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tbdlh0413

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[ÇóÖú] άÆÕÇóÖú ÒÑÓÐ1È˲ÎÓë

13C NMR (126 MHz, cdcl3) ¦Ä 12.06,12.28,14.15,15.39,15.45,17.59,18.27,18.72,18.91,19.00,20.23,20.55,21.12,21.24,22.72,24.38,24.75,25.43,28.21,28.95,29.10,29.27,29.39,29.47,29.62,29.68,29.72,30.28,30.58,31.46,32.44,33.72,35.90,36.20,38.84,39.07,39.69,40.53,42.22,51.25,55.95,55.99,56.10,56.87,129.27,138.35
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1 .     5,6¦Â-Epoxysitosteryl oleate
C47H82O3     ÏàËÆ¶È:76.0%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (3¦Â,22E)-stigmasta-5,9(11),22-trien-3-yl heptadecanoate
C46H78O2     ÏàËÆ¶È:73.9%
Chemistry & Biodiversity          2007          Vol. 4          1578
New Lipoxygenase-Inhibiting Constituents from Calligonum polygonoides
Mirza Arfan Yawer, Ejaz Ahmed, Abdul Malik, Muhammad Ashraf, Muhammad Azam Rasool, and Nighat Afza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (3¦Â)-lup-20(29)-en-3-yl stearate
    ÏàËÆ¶È:73.9%
Helvetica Chimica Acta          2007          Vol. 90          652
Triterpene Esters Isolated from Leaves of Maytenus salicifolia Reissek
Roqueline Rodrigues Silva de Miranda, Gr¨¢cia Divina de F¨¢tima Silva, Lucienir Pains Duarte, and SidneyA ugusto Vieira Filho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     5,6¦Â-Epoxysitosteryl-9,10-dihydroxystearate
C47H84O5     ÏàËÆ¶È:73.9%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     12-ursadien-3¦Â-ol 3-O-palmitate
C46H78O2     ÏàËÆ¶È:71.7%
Chemical & Pharmaceutical Bulletin          2003          51(7) 885¡ª887         
Studies on the Constituents of Gentiana Species. II. A New Triterpenoid, and (S)-(1)- and (R)-(2)-Gentiolactones from Gentiana lutea
Rie KAKUDA, Koichi MACHIDA, Yasunori YAOITA, Masafumi KIKUCHI, and Masao KIKUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Sitosteryl oleate
C47H82O2     ÏàËÆ¶È:71.7%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     ¦Â-sitosterol palmitate
C45H80O2     ÏàËÆ¶È:71.7%
China Journal of Chinese Materia Medica          2002          27          752-754
Studies on the Chemical Constituents in Radix Astilbes Chinensis
SUN Hongxiang, YE Yiping, YANG Ke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 1-5
    ÏàËÆ¶È:71.7%
Bioscience, Biotechnology, and Biochemistry          2001          65          1198-1201
Lupeol Esters from the Twig Bark of Japanese Pear (Pyrus serotina Rehd.) cv. Shinko
Hideyuki TOMOSAKA, Hiroyuki KOSHINO, Tatsuharu TAJIKA, Saburo OMATA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     lupenyl palmitate
    ÏàËÆ¶È:71.7%
Natural Product Research and Development          2006          18          954-957
Studies on Chemical Constituents of Poacynum hendersonii
ZHANG Yun-feng; WEI Dong; GUO Si-yuan; CHEN Feng; DU Nian-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (6R,E)-6-((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-(palmitoyloxy)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-3-ethyl-2-methylhept-4-enoic acid
C45H78O4     ÏàËÆ¶È:71.7%
Life Sciences          2013          92          202-210
Antiulcer and antioxidant activities of a new steroid from Morus alba
Aftab Ahmad, Gaurav Gupta, Muhammad Afzal, Imran Kazmi, Firoz Anwar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Stigmast-5-en-3¦Â-ol linoleate
C17H18O6     ÏàËÆ¶È:70.2%
Acta Botanica Yunnanica          2001          23(3)          368-372
Chemical Constituents from Dysoxylum hainanense
LUO Xiao-Dong,WU Shao-Hua,MA Yun-Bao,WU Da-Gang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     12-ursene-3¦Â, 11a-diol 3-O-palmitate
C46H80O3     ÏàËÆ¶È:69.5%
Chemical & Pharmaceutical Bulletin          2003          51(7) 885¡ª887         
Studies on the Constituents of Gentiana Species. II. A New Triterpenoid, and (S)-(1)- and (R)-(2)-Gentiolactones from Gentiana lutea
Rie KAKUDA, Koichi MACHIDA, Yasunori YAOITA, Masafumi KIKUCHI, and Masao KIKUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     sitosteryl-9,10-dihydroxystearate
C47H84O4     ÏàËÆ¶È:69.5%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     aglycone-II
    ÏàËÆ¶È:69.5%
Yakugaku Zasshi          1983          103          43-48
The Principles of Tetragonia tetragonoides Having an Antiulcerogenic Activity. I. Isolation and Identification of Sterylglucoside Mixture (Compound A)
EMI OKUYAMA, MIKIO YAMAZAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     sitosteryl 9,10-dihydroxystearate
C50H88O4     ÏàËÆ¶È:68.0%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Sitosterol-3-O-12',13'-epoxy-9'-oxo-(10'E)-octadecenoate
C47H78O4     ÏàËÆ¶È:68.0%
Journal of Asian Natural Products Research          2003          5          215-221
THE CHEMICAL CONSTITUENTS OF MUNRONIA HENRYI
SHU-HUA QI, DA-GANG WU, YUN-BAO MA and XIAO-DONG LUO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (3¦Â,5¦Á,6¦Á,22E)-ergosta-7,22-diene-3,5,6-triol 6-oleate
C46H78O4     ÏàËÆ¶È:67.3%
Helvetica Chimica Acta          2007          Vol. 90          1165
New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori
Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     lanoscopariol
C46H80O3     ÏàËÆ¶È:67.3%
Journal of Natural Products          1996          59          181-184
New 9¦Â-Lanostane-Type Triterpenic and 13, 14-seco-Steroidal Esters from the Roots of Artemisia scoparia
Surendra Kumar Sharma and Mohammad Ali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     sambucunlin A
C46H80O2     ÏàËÆ¶È:67.3%
Planta Medica          1988          54          223-224
Antihepatotoxic Principles of Sambucus formosana
Chun-Nan Lin and Whey-Pin Tome
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     Cholesteryl-9,10-dihydroxystearate
C45H80O4     ÏàËÆ¶È:67.3%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     5,6¦Â-Epoxycholesteryl-9,10-dihydroxystearate
C45H80O5     ÏàËÆ¶È:67.3%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     3b-linoleyloxyergosta-7,22-diene
    ÏàËÆ¶È:67.3%
Phytochemistry          2000          54          603-610
Constituents of various wood-rotting basidiomycetes
Joachim Rösecke, Wilfried A. König
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     3b-linoleyloxyergost-7-ene
    ÏàËÆ¶È:67.3%
Phytochemistry          2000          54          603-610
Constituents of various wood-rotting basidiomycetes
Joachim Rösecke, Wilfried A. König
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     ursa-12-sene-3¦Â,11¦Â-diol 3-O-palmitate
C46H80O3     ÏàËÆ¶È:67.3%
Journal of Asian Natural Products Research          2011          13          105-110
Triterpenoids from Viburnum betulifolium
Jiang Hu; Xuan-Qin Chen; Qin-Shi Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     lupenic palmitate
C46H78O2     ÏàËÆ¶È:67.3%
Journal of Asian Natural Products Research          2012          14          7-13
Two new triterpenoids from Cichorium intybus L. roots
Rajkumari Kumari, Mohammed Ali & Vidhu Aeri
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     ¦Â-sitosteryl-3¦Â-glucopyranoside-6'-O-palmitate
    ÏàËÆ¶È:67.3%
Chinese Traditional and Herbal Drugs          2013          44          2657-2660
Chemical constituents from Cardamine leucantha
ZHENG Cong-cong, SU Yan-fang, CHEN Lei, BI Yan-ping, YANG Fan, XU Jing, YAN Shi-lun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     7¦Â-Hydroxysitosteryl oleate
C47H82O3     ÏàËÆ¶È:66.6%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     5,6¦Â-Epoxysitosteryl-9,10-di-tertbutyldimethylsilyloxystearate
C59H112O5Si2     ÏàËÆ¶È:66.6%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     7¦Â-Hydroxycholesteryl-9,10-di-tertbutyldimethylsilyloxystearate
C57H108O5Si2     ÏàËÆ¶È:66.6%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     3¦Â-palmitoyl-11-carboyl-urs-12-ene
C46H78O3     ÏàËÆ¶È:65.9%
Natural Product Research and Development          1997          9(3)          19-23
TRITERPENE ESTERS AND TRITERPENES FROM ILEX KUDINCHA
Ouyang Mingan; Wang Hanqing Su Junhua Liu Yuqing; Yang Chongren
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     (3¦Â)-urs-12-en-3-yl stearate
    ÏàËÆ¶È:65.2%
Helvetica Chimica Acta          2007          Vol. 90          652
Triterpene Esters Isolated from Leaves of Maytenus salicifolia Reissek
Roqueline Rodrigues Silva de Miranda, Gr¨¢cia Divina de F¨¢tima Silva, Lucienir Pains Duarte, and SidneyA ugusto Vieira Filho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     11 ,12 :13 ,28-diepoxyoleanan-3 -yl (9Z)-hexadec-9-enoate
C46H76O4     ÏàËÆ¶È:65.2%
Helvetica Chimica Acta          2004          Vol. 87          46
Palmitoleate (=(9Z)-Hexadeca-9-enoate) Esters of Oleanane Triterpenoids from the Golden Flowers of Tagetes erecta: Isolation and Autoxidation Products
Shaheen Faizi and Aneela Naz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     13 ,28-epoxyolean-11-en-3 -yl (9Z)-hexadec-9-enoate
C46H76O3     ÏàËÆ¶È:65.2%
Helvetica Chimica Acta          2004          Vol. 87          46
Palmitoleate (=(9Z)-Hexadeca-9-enoate) Esters of Oleanane Triterpenoids from the Golden Flowers of Tagetes erecta: Isolation and Autoxidation Products
Shaheen Faizi and Aneela Naz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     7¦Â-Hydroxysitosteryl-9,10-dihydroxystearate
C47H84O5     ÏàËÆ¶È:65.2%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     ¦Â-sitosteryl-3¦Â-glucopyranoside-6'-O-palmitate
    ÏàËÆ¶È:65.2%
Fitoterapia          2004          75          500-504
Cytotoxic constituents from Plumbago zeylanica
A.T. Nguyen , H. Malonne , P. Duez , R. Vanhaelen-a,b, b a anhaelen-Fastrea,M. Vanhaelen, J. Fontaine
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     cholestery 9,12-octadecadienoate
    ÏàËÆ¶È:65.2%
Chinese Pharmaceutical Journal          2011          46          17-20
Studies on Chemical Constituents of Sarcopyramis nepdensis
ZHANG Jin-wen, CHEN Hua-dong, LIAO Mei, ZHANG Yong-hui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     cholesteryl hepadecanoate
    ÏàËÆ¶È:65.2%
Chinese Pharmaceutical Journal          2011          46          17-20
Studies on Chemical Constituents of Sarcopyramis nepdensis
ZHANG Jin-wen, CHEN Hua-dong, LIAO Mei, ZHANG Yong-hui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     3¦Â-palmitoyl-¦Á-amyrin
C46H80O2     ÏàËÆ¶È:65.2%
Natural Product Research and Development          1997          9(3)          19-23
TRITERPENE ESTERS AND TRITERPENES FROM ILEX KUDINCHA
Ouyang Mingan; Wang Hanqing Su Junhua Liu Yuqing; Yang Chongren
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     ¦Â-sitosteryl-3¦Â-glucopyranoside-6'-O-palmitate
    ÏàËÆ¶È:65.2%
Pharmaceutical Chemistry Journal          2012          46          225-227
Chemical constituents of Ficus odorata
P.-W. Tsai, K. A. De Castro-Cruz, C.-C. Shen, C.-T. Chiou, C. Y. Ragasa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     ursa-12-dien-1¦Â,3¦Â-diol 3-O-palmitate
    ÏàËÆ¶È:65.2%
Journal of Asian Natural Products Research          2011          13          105-110
Triterpenoids from Viburnum betulifolium
Jiang Hu; Xuan-Qin Chen; Qin-Shi Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     N,N-dimethyl-(3¦Â-acetate-5¦Â-cholestan)-N-tetradecylammonium bromide
C43H79NO2Br2     ÏàËÆ¶È:65.2%
Molecules          2013          18          14961-14976
Synthesis, Spectroscopic and Semiempirical Studies of New Quaternary Alkylammonium Conjugates of Sterols
Bogumił Brycki, Hanna Koenig, Iwona Kowalczyk and Tomasz Pospieszny
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,7¦Á-dihydroxy-5¦Â-cholan-24-oate
C51H81NO6     ÏàËÆ¶È:64.7%
Steroids          2009          74          424-434
Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids
Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     (3¦Â)-olean-18-en-3-yl stearate
    ÏàËÆ¶È:64.5%
Helvetica Chimica Acta          2007          Vol. 90          652
Triterpene Esters Isolated from Leaves of Maytenus salicifolia Reissek
Roqueline Rodrigues Silva de Miranda, Gr¨¢cia Divina de F¨¢tima Silva, Lucienir Pains Duarte, and SidneyA ugusto Vieira Filho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     3¦Â-stearyloxy-urs-12-ene
C48H84O2     ÏàËÆ¶È:64.5%
Magnetic Resonance in Chemistry          2006          44          127-131
Structural determination of 3¦Â-stearyloxy-urs-12-ene from Maytenus salicifolia by 1D and 2D NMR and quantitative 13C NMR spectroscopy (pages 127¨C131)
R. R. S. Miranda, G. D. F. Silva, L. P. Duarte, I. C. P. Fortes and S. A. Vieira Filho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     (cis)-2-(4-{2-[(ethoxycarbonyl)amino]ethoxy}benzyl)cyclohexyl (3¦Â,22E)-stigmasta-5,22-dien-3-yl butanedioate
    ÏàËÆ¶È:64.5%
Bioorganic & Medicinal Chemistry          2010          18          8194-8203
Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids
Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     ¦Â-sitosterol linoleate
    ÏàËÆ¶È:63.8%
Chinese Pharmaceutical Journal          2007          42          661-663
Studies on Chemical Constituents of Paeonia veitchii L.
WANG Rui, CHOU Gui-xin, ZHU En-yuan, WANG Zheng-tao, BI Kai-shun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     stigmasterol
C64H98O5S2     ÏàËÆ¶È:63.8%
Molecules          2011          16          9404-9420
Succinobucol¡¯s New Coat ¡ª Conjugation with Steroids to Alter Its Drug Effect and Bioavailability
Ondřej Jurček, Satu Ikonen, Lucie Buřičov¨¢, Martina Wimmerov¨¢, Zden¨§k Wimmer, Pavel Drašar, Jan Horn¨ªček, Ad¨¦la Galand¨¢kov¨¢, Jitka Ulrichov¨¢ and Erkki T. Kolehmainen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     ¦Â-sitosteryl linoleate
    ÏàËÆ¶È:63.8%
Natural Product Research and Development          2012          24          1738-1742
Chemical Constituents of Ceratocarpus arenarius L£®
LIU Shan-shan, SUN Wen, YANG Hong-bing*, SUN Wan-fu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     cholesteryl-9,10 dihydroxystearate
C48H84O4     ÏàËÆ¶È:63.2%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     stigmast-5-ene-7¦Á,22¦Á-diol-3¦Â-tetradecanoate
C43H76O4     ÏàËÆ¶È:63.0%
Helvetica Chimica Acta          2008          Vol. 91          1894
Four New Compounds from Sinacalia tangutica
Ying Zhu, Yan Zhao, Guo-Du Huang, and Wang-Suo Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     (3¦Â,5¦Á,6¦Á,22E)-ergosta-7,22-diene-3,5,6-triol 6-linoleate
C46H76O4     ÏàËÆ¶È:63.0%
Helvetica Chimica Acta          2007          Vol. 90          1165
New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori
Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-oleate
    ÏàËÆ¶È:63.0%
Helvetica Chimica Acta          2007          Vol. 90          1165
New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori
Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     28-hydroxy-11-oxoolean-12-en-3 -yl (9Z)-hexadec-9-enoate
C46H76O4     ÏàËÆ¶È:63.0%
Helvetica Chimica Acta          2004          Vol. 87          46
Palmitoleate (=(9Z)-Hexadeca-9-enoate) Esters of Oleanane Triterpenoids from the Golden Flowers of Tagetes erecta: Isolation and Autoxidation Products
Shaheen Faizi and Aneela Naz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     ¦Á-amyrin hexacosoate
    ÏàËÆ¶È:63.0%
Journal of Chinese Pharmaceutical Sciences          2000          9          131-133
A New Triterpene from Rosemary (Rosmarinus officinalis)
Zhou Qunfang, Xu Zhanhui, Tu Pengfei, Li Gansun and Chen Hongming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     ¦Â-sitosteryl-D-glucoside-6'-palmitate
C51H90O7     ÏàËÆ¶È:63.0%
China Journal of Chinese Materia Medica          2006          31          307-308
Studies on the chemical constituents from stem of Chirta longgangensis var. hongyao
WANG Manyuan, YANG Lan, TU Youyou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     ¦Â-Sitosterylpalmitate
    ÏàËÆ¶È:63.0%
Phytochemistry          1998          49          1069-1078
Polyphenols and alkaloids from piper species
Virinder S. Parmar, Subhash C. Jain, Sangita Gupt¦Á, Sangeeta Talwar, Vivek K. Rajwanshi, Rajesh Kumar, Abul Azim, Sanjay Malhotr¦Á, Naresh Kumar, Rajni Jain, Nawal K. Sharm¦Á, Om D. Tyagi, Stephen J. Lawrie, William Errington, Oliwer W. Howarth, Carl E. Ols
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     ¦Â-Sitosterol glucoside 6'-O-palmitate
    ÏàËÆ¶È:63.0%
Korean Journal of Pharmacognosy          2008          39(3)          186-193
Phytochemical Studies on Astragalus Root (3);Triterpenoids and Sterols
Jung, Hye-Sil; Lee, Eun-Ju; Lee, Je-Hyun; Kim, Ju-Sun; Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
58 .     3,5-¶þôÇ»ù¶þÊ®ÍéËáÓðÉȶ¹´¼õ¥
C50H88O4     ÏàËÆ¶È:63.0%
Chemical Journal of Chinese Universities          2003          24          436-441
Chemical Constituents from the Roots of Biondia Hemsleyana
TAN Xing-Gen, ZHANG Xiao-Rong, PENG Shu-Lin, LIAO Xun, DING Li-Sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
59 .     2,3-seco-28-methoxycarbonyl-1-cyanolup-20(29)-en-3-al
C42H69N3O3     ÏàËÆ¶È:63.0%
Chemistry of Natural Compounds          2010          46          39-43
Synthesis of acylhydrazones from lupane and 19¦Â,28-epoxy-18¦Á-oleanane 2,3-seco-aldehydonitriles
I. A. Tolmacheva, N. V. Galaiko and V. V. Grishko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
60 .     ursa-12-sene-1¦Â,3¦Â,11a-triol 3-O-palmitate
C46H80O4     ÏàËÆ¶È:63.0%
Journal of Asian Natural Products Research          2011          13          105-110
Triterpenoids from Viburnum betulifolium
Jiang Hu; Xuan-Qin Chen; Qin-Shi Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
61 .     5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,6¦Á-dihydroxy-5¦Â-cholan-24-oate
C51H81NO6     ÏàËÆ¶È:62.7%
Steroids          2009          74          424-434
Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids
Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
62 .     Ginsenoside DM1
    ÏàËÆ¶È:62.5%
Molecules          2007          12          2140-2150
Isolation, Synthesis and Structures of Cytotoxic Ginsenoside Derivatives
Jun Lei, Xiang Li, Xiao-jie Gong and Yi-nan Zheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
63 .     7¦Â-tert-Butyldimethylsilyloxysitosteryl oleate
C53H96O3Si     ÏàËÆ¶È:62.5%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
64 .     urs-12-en-3¦Â-O-9E,12E-octadecadienoate
C19H34O2     ÏàËÆ¶È:62.5%
Journal of Asian Natural Products Research          2009          11          583-587
A new lipid and other constituents from the rhizomes of Nelumbo nucifera
Prabir Kumar Chaudhuri and Deepika Singh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
65 .     cycloeucalenol vernolitate
C48H80O3     ÏàËÆ¶È:62.5%
Journal of the Chinese Chemical Society          2000          47          555-560
The Chemical Constituents from the Heartwood of Eucalyptus citriodora
Ching-Kuo Lee* and Ming-Huey Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
66 .     3¦Â,12¦Â,20(S)-trihydroxy-dammar-24-ene 20-O-¦Â-D-glucopyranosyl 6'-lauroyl ester
C48H84O9     ÏàËÆ¶È:62.5%
Molecules          2013          18          3689-3702
Synthesis of Esters of Ginsenoside Metabolite M1 and Their Cytotoxicity on MGC80-3 Cells
Wen-Fang Li, Li-Rong Chen, Xiao-Jie Gong, Zheng-Ning Li and Ke-Ke Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
67 .     Ginsenosides 3c
C48H84O9     ÏàËÆ¶È:62.5%
Chinese Journal of Natural Medicines          2011          9          199-203
Synthesis and Structural Analysis of Mono-dodecanoic Acid Esters of Ginsenoside M1
LI Wen-Fang, LI Zheng-Ning, Chen Li-Rong, GONG Xiao-Jie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
68 .     cholesterol
C64H100O5S2     ÏàËÆ¶È:61.7%
Molecules          2011          16          9404-9420
Succinobucol¡¯s New Coat ¡ª Conjugation with Steroids to Alter Its Drug Effect and Bioavailability
Ondřej Jurček, Satu Ikonen, Lucie Buřičov¨¢, Martina Wimmerov¨¢, Zden¨§k Wimmer, Pavel Drašar, Jan Horn¨ªček, Ad¨¦la Galand¨¢kov¨¢, Jitka Ulrichov¨¢ and Erkki T. Kolehmainen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
69 .     3-O-[(9Z)-hexadec-9-enoyl]erythrodiol
C46H78O3     ÏàËÆ¶È:60.8%
Helvetica Chimica Acta          2004          Vol. 87          46
Palmitoleate (=(9Z)-Hexadeca-9-enoate) Esters of Oleanane Triterpenoids from the Golden Flowers of Tagetes erecta: Isolation and Autoxidation Products
Shaheen Faizi and Aneela Naz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
70 .     ¦Â-sitosteryl-3-O-¦Â-D-glucopyranoside-2'-O-palmitate
C51H90O7     ÏàËÆ¶È:60.8%
Phytochemistry          2008          69          2627-2633
Non-cannabinoid constituents from a high potency Cannabis sativa variety
Mohamed M. Radwan, Mahmoud A. ElSohly, Desmond Slade, Safwat A. Ahmed, Lisa Wilson,Abir T. El-Alfy, Ikhlas A. Khan, Samir A. Ross
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
71 .     artemisterol B
C44H72O4     ÏàËÆ¶È:60.8%
Journal of Natural Products          1996          59          181-184
New 9¦Â-Lanostane-Type Triterpenic and 13, 14-seco-Steroidal Esters from the Roots of Artemisia scoparia
Surendra Kumar Sharma and Mohammad Ali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
72 .     N'-{N-[3-Oxo-20(29)-lupen-28-oyl]-9-aminononanoyl}-3-amino-3-phenylpropionic acid
    ÏàËÆ¶È:60.8%
Chemistry of Natural Compounds          2002          38          331-339
SYNTHESIS OF BETULONIC ACID DERIVATIVES CONTAINING AMINO-ACID FRAGMENTS
N. I. Petrenko, N. V. Elantseva, V. Z. Petukhova,M. M. Shakirov, E. E. Shul'ts, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
73 .     7-Ketositosteryl-9,10-dihydroxystearate
C47H82O5     ÏàËÆ¶È:60.8%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
74 .     7-Ketocholesteryl-9,10-dihydroxystearate
C45H78O5     ÏàËÆ¶È:60.8%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
75 .     3b-linoleyloxyergosta-7,24(28)-diene
    ÏàËÆ¶È:60.8%
Phytochemistry          2000          54          603-610
Constituents of various wood-rotting basidiomycetes
Joachim Rösecke, Wilfried A. König
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
76 .     3¦Â-stearoyl-panaxdiol
C48H86O4     ÏàËÆ¶È:60.8%
Chemical Research in Chinese Universities          2007          23          176-182
Synthesis and Primary Research on Antitumor Activity of Three New Panaxadiol Fatty Acid Esters
ZHANG Chun-hong, LIXiang-gao,GAO Yu-gang,ZHANG Lian-xue and FU Xue-qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
77 .     Cyclotucanol 3-palmitate
C47H82O3     ÏàËÆ¶È:60.8%
Planta Medica          2010          76          721-725
Anti-HIV©\1 Diterpenoids from Leaves and Twigs of Polyalthia sclerophylla
Saepou, Siriporn; Pohmakotr, Manat; Reutrakul, Vichai; Yoosook, Chalobon; Kasisit, Jitra; Napaswad, Chanita; Tuchinda, Patoomratana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
78 .     24-Ethyl-22-dehydrocholestanol-acetate
    ÏàËÆ¶È:60.8%
Steroids          1989          53          625-638
Sterols of some Clerodendrum species(verbenaceae): Occurrence of the 24¦Á- and 24¦Â-epimers of 24-ethylsterols lacking a ¦¤25-bond
Toshihiro Akihisa, Yuzuru Matsubara, Parthasarathi Ghosh, Swapnadip Thakur, Toshitake Tamura, Taro Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
79 .     ¦Â-ÏãÊ÷Ö¬ËØ×Ø¸éËáõ¥
    ÏàËÆ¶È:60.8%
Chinese Traditional and Herbal Drugs          2006          37          338-340
Chemical constituents in Ixeridium gramineum
LIU Jun-xi; WEI Xiao-ning; LU Run-hua; SHI Yan-ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
80 .     ¦Â-sitosterol-3-O-¦Â-D-glucoside-6'-O-eicosanate
    ÏàËÆ¶È:60.8%
Chinese Traditional and Herbal Drugs          2002          33          6-8
New steroid glycoside derivatives from Stelmatocrypton khasianum
New steroid glycoside derivatives from Stelmatocrypton khasianum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
81 .     ursa-12-ene-11-one-3-ol-octocosate
    ÏàËÆ¶È:60.8%
Chinese Traditional and Herbal Drugs          2001          32          6-9
Studies on triterpenoids and steroids from Balanophora involucrata
XIA Xin zhong; HAN Hong xing; TU Peng fei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
82 .     2,3-seco-28-methoxycarbonyl-1-cyanolup-20(29)-en-3-al
C46H77N3O3     ÏàËÆ¶È:60.8%
Chemistry of Natural Compounds          2010          46          39-43
Synthesis of acylhydrazones from lupane and 19¦Â,28-epoxy-18¦Á-oleanane 2,3-seco-aldehydonitriles
I. A. Tolmacheva, N. V. Galaiko and V. V. Grishko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
83 .     amphiphilic hexasubstituted [60]fullerene
C412H576O38     ÏàËÆ¶È:60.8%
Tetrahedron Letters          2005          46          6507-6510
Interfacial behavior and film-forming properties of an amphiphilic hexasubstituted [60]fullerene
Delphine Felder-Flesch, Cyril Bourgogne, Jean-Louis Gallani, Daniel Guillon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
84 .     3¦Â-O-{4-[(6-hydroxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-chromen-2-yl)methoxy]-4-oxobutanoyl}betulinic acid
C48H70O8     ÏàËÆ¶È:60.8%
Russian Journal of Organic Chemistry          2010          46          1355-1363
Synthesis of triterpene acids conjugates with ¦Á-tocopherol synthetic analogs
A. Yu. Spivak, R. R. Mufazzalova, E. R. Shakurova and V. N. Odinokov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
85 .     6'-palmitoxyl-¦Â-daucosterin
    ÏàËÆ¶È:60.8%
Journal of the Chinese Chemical Society          2008          55          863-870
Diversity of Chemical Constituents from Saxifraga montana H.
Jun-Xi Liu, Duo-Long Di* and Yan-Ping Shi*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
86 .     compound 1A
C43H66O10     ÏàËÆ¶È:60.8%
Journal of the Indian Chemical Society          2006          83          513-516
Chemical investigation of the roots of Xanthium strumarium
Sankar Kumar Maitra,B.N.Chatterjee,Debi Chakravarti and B.C.Maiti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
87 .     16¦Â-hydroxypseudotaraxasterol 3-O-palmitate
C46H80O3     ÏàËÆ¶È:60.8%
Shoyakugaku Zasshi          1990          44          335-338
Studies on the Constituents of Chrysanthemi Flos
YAHARA SHOJI, MORITA YASUSHI,NOHARA TOSHIHIRO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
88 .     Spirost-5-en-3¦Â-yl N-(2-(4-Isobutyl-phenyl)-propionyl)-6-aminohexanoic Acid
46H69NO5     ÏàËÆ¶È:60.8%
Chemical & Pharmaceutical Bulletin          2013          61          532-538
Synthesis of Diosgenin-Ibuprofen Derivatives and Their Activities against Insulin-Dependent Diabetes Mellitus
Guang Xin, Yanyan Wang, Xiurong Guo, Baozhan Huang, Dan Du, Shiliang He, Rui Zhang, Zhihua Xing, Hang Zhao, Qianming Chen, Wen Huang, Yang He
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
89 .     N,N-dimethyl-(3¦Â-acetate-ergosta-5,7,12-triene)-N-tetradecylammonium bromide
C46H79NO2Br2     ÏàËÆ¶È:60.8%
Molecules          2013          18          14961-14976
Synthesis, Spectroscopic and Semiempirical Studies of New Quaternary Alkylammonium Conjugates of Sterols
Bogumił Brycki, Hanna Koenig, Iwona Kowalczyk and Tomasz Pospieszny
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
90 .     7-ketositosteryl-9,10-dihydroxystearate
C50H86O5     ÏàËÆ¶È:60.7%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
91 .     5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,7¦Â-dihydroxy-5¦Â-cholan-24-oate
C51H81NO6     ÏàËÆ¶È:60.7%
Steroids          2009          74          424-434
Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids
Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
92 .     balanoinvolin
    ÏàËÆ¶È:60.7%
Journal of Anhui Agricultural Sciences          2012          40          9641-9643
Study on the Chemical Constituents of Mirabilis himalaica Roots
YANG Pan-pan et al
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
93 .     3¦Â,12¦Â,20(S)-trihydroxy-dammar-24-ene 20-O-¦Â-D-glucopyranosyl 3'-lauroyl ester
C48H84O9     ÏàËÆ¶È:60.4%
Molecules          2013          18          3689-3702
Synthesis of Esters of Ginsenoside Metabolite M1 and Their Cytotoxicity on MGC80-3 Cells
Wen-Fang Li, Li-Rong Chen, Xiao-Jie Gong, Zheng-Ning Li and Ke-Ke Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
94 .     3¦Â,12¦Â,20(S)-trihydroxy-dammar-24-ene 20-O-¦Â-D-glucopyranosyl 4'-lauroyl ester
C48H84O9     ÏàËÆ¶È:60.4%
Molecules          2013          18          3689-3702
Synthesis of Esters of Ginsenoside Metabolite M1 and Their Cytotoxicity on MGC80-3 Cells
Wen-Fang Li, Li-Rong Chen, Xiao-Jie Gong, Zheng-Ning Li and Ke-Ke Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
95 .     Ginsenosides 3a
C48H84O9     ÏàËÆ¶È:60.4%
Chinese Journal of Natural Medicines          2011          9          199-203
Synthesis and Structural Analysis of Mono-dodecanoic Acid Esters of Ginsenoside M1
LI Wen-Fang, LI Zheng-Ning, Chen Li-Rong, GONG Xiao-Jie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
96 .     Ginsenosides 3b
C48H84O9     ÏàËÆ¶È:60.4%
Chinese Journal of Natural Medicines          2011          9          199-203
Synthesis and Structural Analysis of Mono-dodecanoic Acid Esters of Ginsenoside M1
LI Wen-Fang, LI Zheng-Ning, Chen Li-Rong, GONG Xiao-Jie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
97 .     aglycone-II-Ac
    ÏàËÆ¶È:60.4%
Yakugaku Zasshi          1983          103          43-48
The Principles of Tetragonia tetragonoides Having an Antiulcerogenic Activity. I. Isolation and Identification of Sterylglucoside Mixture (Compound A)
EMI OKUYAMA, MIKIO YAMAZAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
98 .     (R)-2-((R)-1-acetoxy-17-{(1S,2R)-2-[(1S,20S,21S)-20-(tetrahydro-2H-pyran-2-yl)-1,21-dimethyl-nonatriacontyl]cyclopropyl}heptadecyl)hexacosnoic acid methyl ester
C95H184O6     ÏàËÆ¶È:60%
Tetrahedron          2013          69          6285-6296
The synthesis of methoxy and keto mycolic acids containing methyl-trans-cyclopropanes
Gani Koza, Maged Muzael, Richard R. Schubert-Rowles, Cornelia Theunissen, Juma'a R. Al Dulayymi, Mark S. Baird
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
99 .     stigmastanol
C64H102O5S2     ÏàËÆ¶È:59.5%
Molecules          2011          16          9404-9420
Succinobucol¡¯s New Coat ¡ª Conjugation with Steroids to Alter Its Drug Effect and Bioavailability
Ondřej Jurček, Satu Ikonen, Lucie Buřičov¨¢, Martina Wimmerov¨¢, Zden¨§k Wimmer, Pavel Drašar, Jan Horn¨ªček, Ad¨¦la Galand¨¢kov¨¢, Jitka Ulrichov¨¢ and Erkki T. Kolehmainen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
100 .     3¦Â-O-{4-[2-(6-hydroxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-chromen-2-yl)ethoxy]-4-oxobutanoyl}betulinic acid
C49H72O8     ÏàËÆ¶È:59.5%
Russian Journal of Organic Chemistry          2010          46          1355-1363
Synthesis of triterpene acids conjugates with ¦Á-tocopherol synthetic analogs
A. Yu. Spivak, R. R. Mufazzalova, E. R. Shakurova and V. N. Odinokov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
101 .     7¦Â,15¦Á-dihydroxy-lup-20(29)-en-3¦Â-O-eicosanoate
C50H88O4     ÏàËÆ¶È:59.1%
Phytochemistry Letters          2011          4          357-362
Steroids and triterpenoids from Eastern Nigeria mistletoe, Loranthus micranthus Linn. (Loranthaceae) parasitic on Kola acuminata with immunomodulatory potentials
Omeje Edwin Ogechukwu, Osadebe Patience Ogoamaka, Nworu Chukwuemeka Sylvester, Amal Hassan, Abdessamad Debbab, Esimone Charles Okechukwu, Akira Kawamura, Proksch Peter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
102 .     (R)-2-{(R)-1-hydroxy-17-[(1S,2R)-2-((1S,20S,21S)-20-(tetrahydro-2H-pyran-2-yl)-1,21-dimethylnonatriacontyl)cyclopropyl]heptadecyl}hexacosanoic acid
C92H180O5     ÏàËÆ¶È:59.1%
Tetrahedron          2013          69          6285-6296
The synthesis of methoxy and keto mycolic acids containing methyl-trans-cyclopropanes
Gani Koza, Maged Muzael, Richard R. Schubert-Rowles, Cornelia Theunissen, Juma'a R. Al Dulayymi, Mark S. Baird
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
103 .     5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,12¦Á-dihydroxy-5¦Â-cholan-24-oate
C51H81NO6     ÏàËÆ¶È:58.8%
Steroids          2009          74          424-434
Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids
Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
104 .     3¦Â-O-{4-[(6-benzyloxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-chromen-2-yl)methoxy]-4-oxobutanoyl}betulinic acid
C55H76O8     ÏàËÆ¶È:58.8%
Russian Journal of Organic Chemistry          2010          46          1355-1363
Synthesis of triterpene acids conjugates with ¦Á-tocopherol synthetic analogs
A. Yu. Spivak, R. R. Mufazzalova, E. R. Shakurova and V. N. Odinokov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
105 .     (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-palmitate
C44H76O4     ÏàËÆ¶È:58.6%
Helvetica Chimica Acta          2007          Vol. 90          1165
New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori
Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
106 .     (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-stearate
C46H80O4     ÏàËÆ¶È:58.6%
Helvetica Chimica Acta          2007          Vol. 90          1165
New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori
Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
107 .     (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-linoleate
    ÏàËÆ¶È:58.6%
Helvetica Chimica Acta          2007          Vol. 90          1165
New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori
Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
108 .     3-O-tetradecanoyl-16-O-acetylisoiridogermanal
C46H78O6     ÏàËÆ¶È:58.6%
Journal of Natural Products          1999          62          89-93
Iridal-Type Triterpenoids with Ichthyotoxic Activity from Belamcanda chinensis
Hideyuki Ito, Satomi Onoue, Yoko Miyake, and Takashi Yoshida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
109 .     compound 3e
    ÏàËÆ¶È:58.6%
Chemistry of Natural Compounds          2002          38          331-339
SYNTHESIS OF BETULONIC ACID DERIVATIVES CONTAINING AMINO-ACID FRAGMENTS
N. I. Petrenko, N. V. Elantseva, V. Z. Petukhova,M. M. Shakirov, E. E. Shul'ts, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
110 .     N-[3¦Â-acetoxy-20(29)-lupen-28-oyl]-9-amino acid Methyl Ester
    ÏàËÆ¶È:58.6%
Chemistry of Natural Compounds          2002          38          331-339
SYNTHESIS OF BETULONIC ACID DERIVATIVES CONTAINING AMINO-ACID FRAGMENTS
N. I. Petrenko, N. V. Elantseva, V. Z. Petukhova,M. M. Shakirov, E. E. Shul'ts, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
111 .     Z-L-Met-l-Ala-O-cholesterol
C43H66N2O5S     ÏàËÆ¶È:58.6%
Steroids          2006          71          660-669
Efficient microwave assisted access to chiral O-(¦Á-protected-aminoacyl)steroids
Alan R. Katritzky, Parul Angrish
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
112 .     3¦Â-Acetoxy-7¦Â-tert-butyldimethylsilyloxystigma-5-ene
C37H66O3Si     ÏàËÆ¶È:58.6%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
113 .     7-ketocholesteryl-9,10-dihydroxystearate
C48H82O5     ÏàËÆ¶È:58.6%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
114 .     5,6¦Â-Epoxycholesteryl-9,10-di-tertbutyldimethylsilyloxystearate
C57H108O5Si2     ÏàËÆ¶È:58.6%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
115 .     24,26-cyclo-5¦Á-cholest-(22E)-en-3¦Â-ol 4',8',12'-trimethyltridecanoate
C43H74O2     ÏàËÆ¶È:58.6%
Journal of Natural Products          1991          Vol 54          1119
New Sterol Ester from a Deep Water Marine Sponge, Xestospongia sp.
Sarath P. Gunasekera, Susan Cranick, Shirley A. Pomponi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
116 .     stigmast-5-en-3-O-¦Â-D-glucopyranoside tetraacetate
C43H68O10     ÏàËÆ¶È:58.6%
Natural Product Sciences          1999          5          124-126
Sterols and Sterol Glycosides from Cuscuta Reflexa
Anis, E.; Mustafa, G.; Ahmed, S.; Nisarullah, Nisarullah; Malik, A.; Afza, N.; Badar, Y.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
117 .     iristectorene E
    ÏàËÆ¶È:58.6%
Phytochemistry          1994          36          425-431
Iristectorenes A and C-G, monocyclic triterpene esters from Iris tectorum
Katsura Seki, Toshiya Tomihari, Kazuo Haga, Ryohei Kaneko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
118 .     Iristectorene B monoacetate
C46H78O6     ÏàËÆ¶È:58.6%
Phytochemistry          1994          36          433-438
Iristectorene B, a monocyclic triterpene ester from Iris tectorum
Katsura Seki, Toshiya Tomihari, Kazuo Haga, Ryohei Kaneko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
119 .     Mixture of 7-oxostigmast-5-en-3¦Â-yl oleate and palmitate
    ÏàËÆ¶È:58.6%
Phytochemistry          1992          31          4263-4274
Cycloartanes and other terpenoids and phenylpropanoids from Monocyclanthus vignei
Hans Achenbach, Dieter Frey
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
120 .     ¦Â-sitosterol-¦Â-D-ghcopyranoside
    ÏàËÆ¶È:58.6%
Phytochemistry          1991          30          1026-1029
A butyrolactone lignan disaccharide from Flacourtia ramontchi  
V. Satyanarayana, G.L.David Krupadanam, G. Srimannarayana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
121 .     compound 3
    ÏàËÆ¶È:58.6%
Korean Journal of Pharmacognosy          1999          30(3)          290-294
Isolation of Acylated Sterylglycosides from the Legumes of Albizzia julibrissin
Kim, Young-Hee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
122 .     3¦Á-Tetrahydropyranyloxy-5¦Â-cholan-24-ol
C29H50O3     ÏàËÆ¶È:58.6%
Steroids          2011          76          291-300
Synthesis and olfactory activity of unnatural, sulfated 5-bile acid derivatives in the sea lamprey (Petromyzon marinus)
Aaron C. Burns, Peter W. Sorensen, Thomas R. Hoye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
123 .     7¦Â,15¦Á-Dihydroxy-lup-20(29)-en-3¦Â-O-stearate
C48H84O4     ÏàËÆ¶È:58.6%
Phytochemistry Letters          2011          4          357-362
Steroids and triterpenoids from Eastern Nigeria mistletoe, Loranthus micranthus Linn. (Loranthaceae) parasitic on Kola acuminata with immunomodulatory potentials
Omeje Edwin Ogechukwu, Osadebe Patience Ogoamaka, Nworu Chukwuemeka Sylvester, Amal Hassan, Abdessamad Debbab, Esimone Charles Okechukwu, Akira Kawamura, Proksch Peter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
124 .     N-{3-[4-(3-(Bisheptylamino)propyl)piperazinyl]pro-pyl}-3-O-acetyl-ursolamide
C56H100N4O3     ÏàËÆ¶È:58.6%
Bioorganic & Medicinal Chemistry          2008          16          771-782
Pharmacomodulation on the 3-acetylursolic acid skeleton: Design, synthesis, and biological evaluation of novel N-{3-[4-(3-aminopropyl)piperazinyl]propyl}-3-O-acetylursolamide derivatives as antimalarial agents
Simone C.B. Gnoatto, Sophie Susplugas, Luciana Dalla Vechia, Thais B. Ferreira, Alexandra Dassonville-Klimpt, Karine R. Zimmer, Catherine Demailly, Sophie Da Nascimento, Jean Guillon, Philippe Grellier, Hugo Verli, Grace Gosmann, Pascal Sonnet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
125 .     Stigmastanol-3¦Â-p-butanoxydihydrocoumaroate
C42H68O3     ÏàËÆ¶È:58.6%
Phytochemical Analysis          2006          17          36-45
Chemical constituents of rice (Oryza sativa) hulls and their herbicidal activity against duckweed (Lemna paucicostata Hegelm 381)
Ill Min Chung, Mohd Ali, Ateeque Ahmad, Jung Dae Lim, Chang Yeon Yu and Jin Seog Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
126 .     24-Ethylcholesterol-acetate
    ÏàËÆ¶È:58.6%
Steroids          1989          53          625-638
Sterols of some Clerodendrum species(verbenaceae): Occurrence of the 24¦Á- and 24¦Â-epimers of 24-ethylsterols lacking a ¦¤25-bond
Toshihiro Akihisa, Yuzuru Matsubara, Parthasarathi Ghosh, Swapnadip Thakur, Toshitake Tamura, Taro Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
127 .     ¦Â-amyrin hexadecanate
    ÏàËÆ¶È:58.6%
Chinese Traditional and Herbal Drugs          2001          32          6-9
Studies on triterpenoids and steroids from Balanophora involucrata
XIA Xin zhong; HAN Hong xing; TU Peng fei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
128 .     3-O-(N-Nonyl)malonamoyl-12¦Â-acetoxy-25-O-(N-nonyl)oxamoyl-3¦Á,25-dihydroxy-(20S,24R)-epoxydammarane
C56H94N2O11     ÏàËÆ¶È:58.6%
Bioorganic & Medicinal Chemistry          2010          18          2964-2975
Papyriferic acid derivatives as reversal agents of multidrug resistance in cancer cells
Juan Xiong, Masatoshi Taniguchi, Yoshiki Kashiwada, Michiko Sekiya, Takashi Yamagishi, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
129 .     6'-linoleic-¦Â-daucosterol
C30H50O     ÏàËÆ¶È:58.6%
Natural Product Research and Development          2009          21          776-778
Chemical Constituents of the Roots of Ligularia fischeri
DENG Mei-cai; JIAO Wei; DONG Wei-wei; LU Run-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
130 .     methyl N-{5-oxo-5-[(3¦Â,22E)-stigmasta-5,22-dien-3-yloxy]pentanoyl}-L-phenylalanine
C44H65NO5     ÏàËÆ¶È:58.6%
Molecules          2011          16          9357-9367
Stigmasterol-Based Novel Low Molecular Weight/Mass Organic Gelators
Jana Šustekov¨¢, Pavel Drašar, David Šaman and Zden¨§k Wimmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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132 .     ¦Â-sitosterol
C62H96O5S2     ÏàËÆ¶È:58.6%
Molecules          2011          16          9404-9420
Succinobucol¡¯s New Coat ¡ª Conjugation with Steroids to Alter Its Drug Effect and Bioavailability
Ondřej Jurček, Satu Ikonen, Lucie Buřičov¨¢, Martina Wimmerov¨¢, Zden¨§k Wimmer, Pavel Drašar, Jan Horn¨ªček, Ad¨¦la Galand¨¢kov¨¢, Jitka Ulrichov¨¢ and Erkki T. Kolehmainen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
133 .     faradiol palmitic ester
    ÏàËÆ¶È:58.6%
Journal of Ethnopharmacology          1997          57          139-144
Anti-oedematous activities of the main triterpendiol esters of marigold (Calendula officinalis L.)
K Zitterl-Eglseer, S Sosa, J Jurenitsch, M Schubert-Zsilavecz, R Della Loggia, A Tubaro, M Bertoldi, C Franz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
134 .     7¦Â,15¦Á-dihydroxyl-lup-20(29)-ene-3¦Â-O-palmitate
C46H80O4     ÏàËÆ¶È:58.6%
Natural Product Research          2012          26          1775-1781
Three hydroxylated lupeol-based triterpenoid esters isolated from the Eastern Nigeria mistletoe parasitic on Kola acuminata
Edwin Ogechukwu Omeje, Patience Ogoamaka Osadebe, Charles Okechukwu Esimone, Chukwuemeka Sylvester Nworu, Akira Kawamura & Peter Proksch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
135 .     3¦Â,12¦Â,20(S)-trihydroxy-dammar-24-ene 20-O-¦Â-D-glucopyranosyl 6'-decanoyl ester
C46H80O9     ÏàËÆ¶È:58.6%
Molecules          2013          18          3689-3702
Synthesis of Esters of Ginsenoside Metabolite M1 and Their Cytotoxicity on MGC80-3 Cells
Wen-Fang Li, Li-Rong Chen, Xiao-Jie Gong, Zheng-Ning Li and Ke-Ke Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
136 .     (3RS,5S)-3-[(8R,11R,12R,15R,16R,19R,20R)-20-(tert-butyldimethylsilyloxy)-12,15;16,19-diepoxy-8,11-bis(methoxymethoxy)-dotriacontanyl]-5-methyl-3-(phenylsulfenyl)tetrahydrofuran-2-one
C53H94O9SSi     ÏàËÆ¶È:58.6%
European Journal of Organic Chemistry          2006          2006          1422-1429
First Total Synthesis of Longimicin D
Hiroaki Tominaga, Naoyoshi Maezaki, Minori Yanai, Naoto Kojima, Daisuke Urabe, Risa Ueki and Tetsuaki Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
137 .     ¦Â-sitosteryl-3-O-¦Â-D-glucopyr-anoside-2'-O-palmitate
C51H90O7     ÏàËÆ¶È:58.6%
Natural Product Research and Development          2014          26          197-201
Chemical Constituents from the Roots of Nothapodytes pittosporoides
BAI Yong-hua, SONG Qi-shi*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
138 .     ¦Á-amyrin 3-O-dimorphecolate
C48H80O3     ÏàËÆ¶È:58.6%
Natural Medicines          2004          58          22-26
Triterpenoids from Gentianae Scabrae Radix and Gentianae Radix
Kakuda Rie,Ueno Chie, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
139 .     Methyl (3¦Â)-3-({6-[(tert-butoxycarbonyl)amino]octanoyl}-oxy)-11-oxoolean-12-en-30-oate
C44H71NO7     ÏàËÆ¶È:58.6%
Zeitschrift f¨¹r Naturforschung B          2012          67          731-746
Synthesis and Cytotoxic Activity of Methyl Glycyrrhetinate Esterified with Amino Acids
Ren¨¦ Csuk, Stefan Schwarz, Bianka Siewert, Ralph Kluge, and Dieter Ströhl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
140 .     fraction a
    ÏàËÆ¶È:58.3%
Chemical & Pharmaceutical Bulletin          1992          40          1773-1778
Marine Natural Products. XXX. Two New 3-Keto-4-methylene Steroids, Theonellasterone and Conicasterone, and a Diels-Alder Type Dimeric Steroid Bistheonellasterone, from the Okinawan Marine Sponge Theonella swinhoei
Motomasa KOBAYASHI,Kazuyoshi KAWAZOE,Taketo KATORI and Isao KITAGAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
141 .     N-(Cholest-5-en-3¦Â-yl)-3¦Â-hydroxyandrost-5-ene-17¦Â-carboxamide
C47H75NO2     ÏàËÆ¶È:57.4%
Steroids          2009          74          88-94
Steroids linked with amide bond¡ªExtended cholesterol
Ivan Černy, Miloš Bud¨§š¨ªnsky, Vladim¨ªr Pouzar, Pavel Drašar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
142 .     3¦Â-palmitoyl-lup-20(29)-ene-24-methyl ester
    ÏàËÆ¶È:57.4%
Natural Product Research and Development          1997          9(3)          19-23
TRITERPENE ESTERS AND TRITERPENES FROM ILEX KUDINCHA
Ouyang Mingan; Wang Hanqing Su Junhua Liu Yuqing; Yang Chongren
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
143 .     6-hydroxy-N'-[3¦Â-hydroxylup-20(29)-en-28-oyl]-2,5,7,8-tetramethyl-3,4-dihydro-2H-chromen-2-carbohydrazide
C44H66N2O5     ÏàËÆ¶È:57.4%
Russian Journal of Organic Chemistry          2010          46          1355-1363
Synthesis of triterpene acids conjugates with ¦Á-tocopherol synthetic analogs
A. Yu. Spivak, R. R. Mufazzalova, E. R. Shakurova and V. N. Odinokov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
144 .     methyl 2-((1R,2R)-1-(tert-butyldimethylsilyloxy)-19-((1S,2R)-2-((2S,18S,19S)-18-methoxy-19-methylheptatriacontan-2-yl)cyclo-propyl)nonadecyl)hexacosanoate
C95H190O4Si     ÏàËÆ¶È:57.4%
Tetrahedron          2013          69          6285-6296
The synthesis of methoxy and keto mycolic acids containing methyl-trans-cyclopropanes
Gani Koza, Maged Muzael, Richard R. Schubert-Rowles, Cornelia Theunissen, Juma'a R. Al Dulayymi, Mark S. Baird
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
145 .     balanoinvolin
C53H90O7     ÏàËÆ¶È:57.1%
Chemistry of Natural Compounds          2009          45          371-373
BALANOINVOLIN, A NEW STEROID DERIVATIVEFROM Balanophora involucrate
Bing Luo, Kun Zou, Zhiyong Guo, Feijun Dan, Juizhi Wang, and Hui Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
146 .     3¦Á-Hydroxy-5¦Â-cholan-24-oic acid (cholan-24-oicacid methyl ester)-3-yl ester
C49H81O5     ÏàËÆ¶È:57.1%
Steroids          2003          68          1157-1161
Synthesis of ester-linked lithocholic acid dimers
Lutfun Nahar, Alan B. Turner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
147 .     GE3
C49H80N8O14     ÏàËÆ¶È:57.1%
The Journal of Antibiotics          1997          50          704-708
GE3, a Novel Hexadepsipeptide Antitumor Antibiotic Produced by Streptomyces sp. II. Structure Determination
TSUTOMU AGATSUMA, YASUSHI SAKAI, TAMIO MIZUKAMI, YUTAKA SAITOH
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
148 .     compound 16
C63H96N8O7     ÏàËÆ¶È:57.1%
Tetrahedron          2014          70          3297-3305
The CuI-catalyzed alkyne¨Cazide cycloaddition as direct conjugation/cyclization method of peptides to steroids
Radell Echemend¨ªa, Odette Concepci¨®n, Fidel E. Morales, M¨¢rcio W. Paixão, Daniel G. Rivera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
149 .     N-(tert-Butoxy)carbonyl]-D-alanyl-N-methyl-L-leucyl-N-methyl-L-leucyl-N-methyl-L-valyl-(2S,3R,4R,6E)-3-hydroxy-4-methyl-2-(methylamino)oct-6-enoyl-(2S)-2-aminobutanoyl-N-methylglycyl-N-methyl-L-leucyloxy-¦×(O CH2)-ethoxy-¦×(O NH)-4,4,4,4',4',4'-hexafluoro-D
    ÏàËÆ¶È:56.8%
Helvetica Chimica Acta          2010          93          1583-1601
Stereoselective Synthesis of [5-[4,4,4,4¡ä,4¡ä,4¡ä-Hexafluoro-N-(2-hydroxyethoxy)-D-valine]]- and [5-[4,4,4,4¡ä,4¡ä,4¡ä-Hexafluoro-N-(2-hydroxyethoxy)-L-valine]cyclosporin A
Marcel K. Eberle and Reinhart Keese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
150 .     artemisterol A
C43H68O5     ÏàËÆ¶È:56.5%
Journal of Natural Products          1996          59          181-184
New 9¦Â-Lanostane-Type Triterpenic and 13, 14-seco-Steroidal Esters from the Roots of Artemisia scoparia
Surendra Kumar Sharma and Mohammad Ali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
151 .     ¦Â-sitosterol ¦Â-D-glucopyranoside tetraacetate
    ÏàËÆ¶È:56.5%
Planta Medica          1993          59          369-372
A New Oleanolic Acid Derivative from Securinega tinctoria
LuisM. Carvalho and J. Seita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
152 .     bistheonellasterone
C60H96O2     ÏàËÆ¶È:56.5%
Chemical & Pharmaceutical Bulletin          1992          40          1773-1778
Marine Natural Products. XXX. Two New 3-Keto-4-methylene Steroids, Theonellasterone and Conicasterone, and a Diels-Alder Type Dimeric Steroid Bistheonellasterone, from the Okinawan Marine Sponge Theonella swinhoei
Motomasa KOBAYASHI,Kazuyoshi KAWAZOE,Taketo KATORI and Isao KITAGAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
153 .     3¦Â-O-(3,4,6-tri-O-acetyl-2-deoxy-¦Á-L-arabinohexopyranosyl)-20(29)-lupen-28-oic acid
C43H66O10     ÏàËÆ¶È:56.5%
Chemistry of Natural Compounds          2006          42          706-709
SYNTHESIS OF METHYL ESTERS OF BETULINIC ACID 2-DEOXY-a-GLYCOSIDES AND 28-OXO-19,28-EPOXYOLEANANE
O. B. Flekhter, N. I. Medvedeva, E. V. Tret'yakova,F. Z. Galin, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
154 .     compound 4e
    ÏàËÆ¶È:56.5%
Chemistry of Natural Compounds          2002          38          331-339
SYNTHESIS OF BETULONIC ACID DERIVATIVES CONTAINING AMINO-ACID FRAGMENTS
N. I. Petrenko, N. V. Elantseva, V. Z. Petukhova,M. M. Shakirov, E. E. Shul'ts, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
155 .     N'-{N-[3-Oxo-20(29)-lupen-28-oyl]-9-aminononanoyl}-3-aminopropionic acid
    ÏàËÆ¶È:56.5%
Chemistry of Natural Compounds          2002          38          331-339
SYNTHESIS OF BETULONIC ACID DERIVATIVES CONTAINING AMINO-ACID FRAGMENTS
N. I. Petrenko, N. V. Elantseva, V. Z. Petukhova,M. M. Shakirov, E. E. Shul'ts, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
156 .     compound 19
    ÏàËÆ¶È:56.5%
Helvetica Chimica Acta          2009          92          839-889
New Derivatives of Ascomycin with Modifications in the Amino Acid Region - Synthesis and Biological Activities, and X-Ray Crystal Structure of 5,6-Dehydroascomycin
Murty A. R. C. Bulusu, Peter Waldstätten, Thomas Tricotet, Christophe Rochais, Andrea Steck, Markus Bacher, Gerhard Schulz, Josef G. Meingassner, Peter Hiestand, Gerhard Zenke, Walter Schuler, Trixie Wagner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
157 .     7-Ketositosteryl oleate
C47H80O3     ÏàËÆ¶È:56.5%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
158 .     7¦Â-Hydroxycholesteryl-9,10-dihydroxystearate
C45H80O5     ÏàËÆ¶È:56.5%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
159 .     atroside
C45H78O7     ÏàËÆ¶È:56.5%
Fitoterapia          2001          72          712-714
A new acylated steroid glucoside from Pero skia atriplicifolia
M.S. Alia, M. Saleema, A.W. Erian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
160 .     (6'-O-palmitoyl)-sitosterol-3-O-¦Â-D-glucoside
    ÏàËÆ¶È:56.5%
Journal of Natural Products          1987          Vol 50          881
Sterols and Steryl Glycosides from Urtica dioica
Neera Chaurasia, Max Wichtl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
161 .     3¦Â-tetradecanoyl erythrodiol
C44H76O3     ÏàËÆ¶È:56.5%
Acta Pharmaceutica Sinica          2009          Vol 44          1258−1261
A new erythrodiol triterpene fatty ester from Scorzonera mongolica
WANG Bin; LI Guo-qiang; GUAN Hua-shi; YANG Li-ye; TONG Guo-zhong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
162 .     24-methylenecholesterol linolenate
C46H76O2     ÏàËÆ¶È:56.5%
Chemical & Pharmaceutical Bulletin          2009          57          401-404
Alpha-Reductase and Aromatase Inhibitory Constituents from Brassica rapa L. Pollen
Yong-Hui Li, Yi-Fang Yang, Kun Li, Li-Li Jin, Nian-Yun Yang and De-Yun Kong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
163 .     compound 3a
    ÏàËÆ¶È:56.5%
Phytochemistry          1990          29          2351-2355
Sterol glucosides from Prunella vulgaris
Hisashi Kojima,Noriko Sato,Akiko Hatano,Haruo Ogura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
164 .     Sitosterol-3-O-¦Â-D-glucosl-6'-O-palmitate
    ÏàËÆ¶È:56.5%
Phytochemical Analysis          1992          3          38-41
Characterization of acylated steryl glycosides from Euryale ferox by nuclear magnetic resonance spectroscopy
Zhao Haoru and Zhao Shoushun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
165 .     Stigmastanol-3¦Â-p-glyceroxydihydrocoumaroate
C41H66O5     ÏàËÆ¶È:56.5%
Phytochemical Analysis          2006          17          36-45
Chemical constituents of rice (Oryza sativa) hulls and their herbicidal activity against duckweed (Lemna paucicostata Hegelm 381)
Ill Min Chung, Mohd Ali, Ateeque Ahmad, Jung Dae Lim, Chang Yeon Yu and Jin Seog Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
166 .     Stigmast-5-en-3-O-¦Â-D-glucoside tetraacetate
    ÏàËÆ¶È:56.5%
Magnetic Resonance in Chemistry          2001          39          399-405
Complete 1H and 13C NMR assignments of stigma-5-en-3-O-¦Â-glucoside and its acetyl derivative
Shaheen Faizi, Muhammad Ali, Rubeena Saleem, Irfanullah and Sarah Bibi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
167 .     (22E,24R,25R)-6-(1,3-Dioxolan-2-yl)-24-methyl-3¦Á,5-cyclo-5¦Á-cholest-22-en-26-oic acid ethyl ester
    ÏàËÆ¶È:56.5%
Steroids          2012          77          780-790
A new approach to the side chain formation of 24-alkyl-22-hydroxy steroids: Application to the preparation of early brassinolide biosynthetic precursors
Alaksiej L. Hurski, Vladimir N. Zhabinskii, Vladimir A. Khripach
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
168 .     3-O-(N-pentyl)malonamoyl-12¦Â-acetoxy-25-O-(N-pen-tyl)oxamoyl-3¦Á,25-dihydroxy-(20S,24R)-epoxydammarane
C47H78N2O9     ÏàËÆ¶È:56.5%
Bioorganic & Medicinal Chemistry          2010          18          2964-2975
Papyriferic acid derivatives as reversal agents of multidrug resistance in cancer cells
Juan Xiong, Masatoshi Taniguchi, Yoshiki Kashiwada, Michiko Sekiya, Takashi Yamagishi, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
169 .     methyl N-{4-oxo-4-[(3¦Â,22E)-stigmasta-5,22-dien-3-yloxy]butanoyl}-L-phenylalanine
C43H63NO5     ÏàËÆ¶È:56.5%
Molecules          2011          16          9357-9367
Stigmasterol-Based Novel Low Molecular Weight/Mass Organic Gelators
Jana Šustekov¨¢, Pavel Drašar, David Šaman and Zden¨§k Wimmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
170 .     3¦Â-oxalyloxy-23,24-bisnorchol-5-en-22-yl-(N-3-methoxycarbonylpropyl)-amine
    ÏàËÆ¶È:56.5%
Bioorganic & Medicinal Chemistry          2009          17          5950-5961
SAR studies on azasterols as potential anti-trypanosomal and anti-leishmanial agents
Federica Gigante, Marcel Kaiser, Reto Brun, Ian H. Gilbert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
171 .     (R)-2-{(R)-17-[(1S,2R)-2-((1S,21S)-1,21-dimethyl-20-oxononatriacontyl)-cyclopropyl]-1-hydroxyheptadecyl}-hexacosanoic acid methyl ester
C90H174O5     ÏàËÆ¶È:56.5%
Tetrahedron          2013          69          6285-6296
The synthesis of methoxy and keto mycolic acids containing methyl-trans-cyclopropanes
Gani Koza, Maged Muzael, Richard R. Schubert-Rowles, Cornelia Theunissen, Juma'a R. Al Dulayymi, Mark S. Baird
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
172 .     Methyl 3¦Á,7¦Á,12¦Á-tris(decanoyloxy)-5¦Â-cholate
C55H96O8     ÏàËÆ¶È:56.5%
Steroids          2011          76          1082-1097
Investigation of new acyloxy derivatives of cholic acid and their esters as drug absorption modifiers
Lech Mr¨®zek, Lenka Dvoř¨¢kov¨¢, Zuzana Mandelov¨¢, Lucie R¨¢rov¨¢, Anna Řez¨¢čov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
173 .     (20¦Á,22¦Â,25R)-3¦Â-Acetoxy-5,6-epoxy-26-azidofurostane
C29H45N3O4     ÏàËÆ¶È:56.5%
Steroids          2012          77          1069-1074
Application of hypoiodite-mediated aminyl radical cyclization to synthesis of solasodine acetate
Yi Kou, Myong Chul Koag, Young Cheun, Aram Shin, Seongmin Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
174 .     N-{3-[4-(3-Aminopropyl)piperazinopropyl]terbutylcarbamate}-3-acetylbetulinamide
C47H80N4O5     ÏàËÆ¶È:56.5%
Molecules          2012          17          12003-12014
Synthesis and Antiplasmodial Activity of Betulinic Acid and Ursolic Acid Analogues
Adrine M. Innocente, Gloria N. S. Silva, Laura Nogueira Cruz, Miriam S. Moraes, Myna Nakabashi, Pascal Sonnet, Grace Gosmann, C¨¦lia R. S. Garcia and Simone C. B. Gnoatto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
175 .     ¦Á-amyrin 3-O-coriolate
C48H80O3     ÏàËÆ¶È:56.5%
Natural Medicines          2004          58          22-26
Triterpenoids from Gentianae Scabrae Radix and Gentianae Radix
Kakuda Rie,Ueno Chie, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
176 .     3¦Â-(Stearyloxy)olean-12-ene
C48H84O2     ÏàËÆ¶È:56.2%
Helvetica Chimica Acta          2003          Vol. 86          3445
3¦Â-(Stearyloxy)olean-12-ene from Austroplenckia populnea: Structure Elucidation by 2D-NMR and Quantitative 13C-NMR Spectroscopy
S. A. Vieira Filho, L. P. Duarte, G. D. F. Silva, O. W. Howarth, and I. S. Lula
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
177 .     iristectorene G
    ÏàËÆ¶È:56.2%
Phytochemistry          1994          36          425-431
Iristectorenes A and C-G, monocyclic triterpene esters from Iris tectorum
Katsura Seki, Toshiya Tomihari, Kazuo Haga, Ryohei Kaneko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
178 .     cycloeucalenol linolenate
C48H78O2     ÏàËÆ¶È:56.2%
Chemical & Pharmaceutical Bulletin          2009          57          401-404
Alpha-Reductase and Aromatase Inhibitory Constituents from Brassica rapa L. Pollen
Yong-Hui Li, Yi-Fang Yang, Kun Li, Li-Li Jin, Nian-Yun Yang and De-Yun Kong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
179 .     7-Ketocholesteryl-9,10-di-tertbutyldimethylsilyloxystearate
C57H106O5Si2     ÏàËÆ¶È:55.3%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
180 .     Benzyl¦Á3¦Á,7¦Á,12¦Á-tris(hexadecanoyloxy)-5¦Â-cholate
C79H136O8     ÏàËÆ¶È:55.3%
Steroids          2011          76          1082-1097
Investigation of new acyloxy derivatives of cholic acid and their esters as drug absorption modifiers
Lech Mr¨®zek, Lenka Dvoř¨¢kov¨¢, Zuzana Mandelov¨¢, Lucie R¨¢rov¨¢, Anna Řez¨¢čov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
181 .     Dimer N
C46H73N3O6     ÏàËÆ¶È:55.3%
Molecules          2013          18          5936-5953
Dimeric Labdane Diterpenes: Synthesis and Antiproliferative Effects
Mariano Walter Pertino, Cristina Theoduloz, Marco Bast¨ªas and Guillermo Schmeda-Hirschmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
182 .     3-Oxo-5¦Â-cholan-24-oic acid (cholan-24-oic acidmethyl ester)-3-yl ester
C49H79O5     ÏàËÆ¶È:55.1%
Steroids          2003          68          1157-1161
Synthesis of ester-linked lithocholic acid dimers
Lutfun Nahar, Alan B. Turner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
183 .     ligustrin C
    ÏàËÆ¶È:55.1%
Phytochemistry          1997          46          977-979
Acylated triterpenoids from Ligustrum ovalifolium
Koichi Machida, Toshio Yamaguchi, Yoshiko Kamiya, Masao Kikuchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
184 .     N'-[3¦Â-acetoxylup-20(29)-en-28-oyl]-6-hydroxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-chromen-2-carbohydrazide
C46H68N2O6     ÏàËÆ¶È:55.1%
Russian Journal of Organic Chemistry          2010          46          1355-1363
Synthesis of triterpene acids conjugates with ¦Á-tocopherol synthetic analogs
A. Yu. Spivak, R. R. Mufazzalova, E. R. Shakurova and V. N. Odinokov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
185 .     codonopilate A
C49H82O3     ÏàËÆ¶È:55.1%
Journal of Natural Medicines          2011          65          18-23
Three new triterpenyl esters, codonopilates A¨CC, isolated from Codonopsis pilosula
Daigo Wakana ,Nobuo Kawahara ,Yukihiro Goda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
186 .     codonopilate B
C49H82O3     ÏàËÆ¶È:55.1%
Journal of Natural Medicines          2011          65          18-23
Three new triterpenyl esters, codonopilates A¨CC, isolated from Codonopsis pilosula
Daigo Wakana ,Nobuo Kawahara ,Yukihiro Goda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
187 .     codonopilate C
C49H80O3     ÏàËÆ¶È:55.1%
Journal of Natural Medicines          2011          65          18-23
Three new triterpenyl esters, codonopilates A¨CC, isolated from Codonopsis pilosula
Daigo Wakana ,Nobuo Kawahara ,Yukihiro Goda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
188 .     Benzyl¦Á3¦Á-acetoxy-7¦Á,12¦Á-bis(hexadecanoyloxy)-5¦Â-cholate
C65H108O8     ÏàËÆ¶È:55.1%
Steroids          2011          76          1082-1097
Investigation of new acyloxy derivatives of cholic acid and their esters as drug absorption modifiers
Lech Mr¨®zek, Lenka Dvoř¨¢kov¨¢, Zuzana Mandelov¨¢, Lucie R¨¢rov¨¢, Anna Řez¨¢čov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
189 .     5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,7¦Á,12¦Á-trihydroxy-5¦Â-cholan-24-oate
C51H81NO7     ÏàËÆ¶È:54.9%
Steroids          2009          74          424-434
Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids
Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
190 .     11-oxoolean-12-en-3 -yl (9Z)-hexadec-9-enoate
C46H76O3     ÏàËÆ¶È:54.3%
Helvetica Chimica Acta          2004          Vol. 87          46
Palmitoleate (=(9Z)-Hexadeca-9-enoate) Esters of Oleanane Triterpenoids from the Golden Flowers of Tagetes erecta: Isolation and Autoxidation Products
Shaheen Faizi and Aneela Naz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
191 .     viridamide A
C46H79N5O10     ÏàËÆ¶È:54.3%
Journal of Natural Products          2008          71(9)          1544-1550
Viridamides A and B, Lipodepsipeptides with Antiprotozoal Activity from the Marine Cyanobacterium Oscillatoria nigro-viridis
T. Luke Simmons, Niclas Engene, Luis David Ureña, Luz I. Romero,Eduardo Ortega-Barr¨ªa, Lena Gerwick, and William H. Gerwick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
192 .     gymnasterone A
C45H67NO5     ÏàËÆ¶È:54.3%
Journal of Natural Products          2007          70          1731-1740
Variation in Cytostatic Constituents of a Sponge-Derived Gymnascella dankaliensis by Manipulating the Carbon Source
Taro Amagata,Makoto Tanaka,Takeshi Yamada, Mitsunobu Doi, Katsuhiko Minoura, Hirofumi Ohishi,Takao Yamori, and Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
193 .     fritillebin A
C42H66O5     ÏàËÆ¶È:54.3%
Chemical & Pharmaceutical Bulletin          1995          43          1148-1153
Structure-Activity Relationships of Neuromedin U. I. Contractile Activity of Dog Neuromedin U-Related Peptides on Isolated Chicken Crop Smooth Muscle
Naoki SAKURA,Katsuro KUROSAWA and Tadashi HASHIMOTO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
194 .     fritillebin B
C44H68O7     ÏàËÆ¶È:54.3%
Chemical & Pharmaceutical Bulletin          1995          43          1148-1153
Structure-Activity Relationships of Neuromedin U. I. Contractile Activity of Dog Neuromedin U-Related Peptides on Isolated Chicken Crop Smooth Muscle
Naoki SAKURA,Katsuro KUROSAWA and Tadashi HASHIMOTO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
195 .     (24S)-[26,27-2H6]23-Phenylsulfonyl-24-methyl-3¦Á ,5-cyclo-5¦Á -cholestan-22-ol
    ÏàËÆ¶È:54.3%
Steroids          2004          69          617-628
Synthesis of [26,27-2H6]brassinosteroids from 23,24-bisnorcholenic acid methyl ester
Andrey P. Antonchick, Bernd Schneider, Vladimir N. Zhabinskii, Vladimir A. Khripach
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
196 .     Z-L-Phe-O-¦Â-Sitosterol
C46H65NO4     ÏàËÆ¶È:54.3%
Steroids          2006          71          660-669
Efficient microwave assisted access to chiral O-(¦Á-protected-aminoacyl)steroids
Alan R. Katritzky, Parul Angrish
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
197 .     colebrin C
C52H90O7     ÏàËÆ¶È:54.3%
Fitoterapia          2000          71          641-648
New steroids from Clerodendrum colebrookianum
Hui Yang, Jia Wang, Ai-Jun Hou, Yun-Pin Guo,Zhong-Wen Lin, Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
198 .     2¦Á-hydroxypyracrenic acid triacetate
C45H60O10     ÏàËÆ¶È:54.3%
Phytochemistry          1996          43          847-851
Three triterpene esters from Zizyphus jujuba
Shoei-Sheng Lee, Buh-Fang Lin, Karin C. Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
199 .     iristectorene B
    ÏàËÆ¶È:54.3%
Phytochemistry          1994          36          425-431
Iristectorenes A and C-G, monocyclic triterpene esters from Iris tectorum
Katsura Seki, Toshiya Tomihari, Kazuo Haga, Ryohei Kaneko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
200 .     Iristectorene B
C44H76O5     ÏàËÆ¶È:54.3%
Phytochemistry          1994          36          433-438
Iristectorene B, a monocyclic triterpene ester from Iris tectorum
Katsura Seki, Toshiya Tomihari, Kazuo Haga, Ryohei Kaneko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
201 .     N-hydroxysolasodine
C27H43NO3     ÏàËÆ¶È:54.3%
Phytochemistry          1992          31          1837-1839
N-Hydroxysolasodine from Solanum robustum
Helmut Ripperger, Andrea Porzel
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
202 .     compound 1a
    ÏàËÆ¶È:54.3%
Phytochemistry          1991          30          1869-1872
Diterpenic adducts from Xylopia species
Wagner Vilegas, Joana D'Arc Felicio, Nidia F. Roque, Hugo E. Gottlieb
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
203 .     sitosteryl-¦Â-D-glucopyranoside tetraacetate
    ÏàËÆ¶È:54.3%
Phytochemistry          1991          30          3383-3387
Steroids and triterpenoids from Rosa laevigata
Jim-Min Fang, Kuang-Chaun Wang, Yu-Shia Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
204 .     7-hydroxysitosteryl-3-O-¦Â-D-glucopyranoside tetraacetate
    ÏàËÆ¶È:54.3%
Phytochemistry          1991          30          3383-3387
Steroids and triterpenoids from Rosa laevigata
Jim-Min Fang, Kuang-Chaun Wang, Yu-Shia Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
205 .     stigmasta-3¦Á,5¦Á-diol-3-O-¦Â-D-glucopyranoside tetraacetate
    ÏàËÆ¶È:54.3%
Phytochemistry          1991          30          3383-3387
Steroids and triterpenoids from Rosa laevigata
Jim-Min Fang, Kuang-Chaun Wang, Yu-Shia Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
206 .     compound 7
    ÏàËÆ¶È:54.3%
Phytochemistry          1988          27          2199-2204
Sesquiterpenoid glycosides and an acetogenin glucoside from Lessingia glandulifera
Shivanand D. Jolad,Barbara N. Timmermann,Joseph J. Hoffmann,Robert B. Bates,Fernando A. Camou,Teruna J. Siahaan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
207 .     compound 3b
    ÏàËÆ¶È:54.3%
Phytochemistry          1990          29          2351-2355
Sterol glucosides from Prunella vulgaris
Hisashi Kojima,Noriko Sato,Akiko Hatano,Haruo Ogura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
208 .     N-{3-[4-(3-(Bis(3-phenylpropyl)amino)propyl)piper-azinyl]propyl}-3-O-acetylursolamide
C60H92N4O3     ÏàËÆ¶È:54.3%
Bioorganic & Medicinal Chemistry          2008          16          771-782
Pharmacomodulation on the 3-acetylursolic acid skeleton: Design, synthesis, and biological evaluation of novel N-{3-[4-(3-aminopropyl)piperazinyl]propyl}-3-O-acetylursolamide derivatives as antimalarial agents
Simone C.B. Gnoatto, Sophie Susplugas, Luciana Dalla Vechia, Thais B. Ferreira, Alexandra Dassonville-Klimpt, Karine R. Zimmer, Catherine Demailly, Sophie Da Nascimento, Jean Guillon, Philippe Grellier, Hugo Verli, Grace Gosmann, Pascal Sonnet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
209 .     N-{3-[4-(3-(Bis(4-nitrobenzyl)amino)propyl)piper-azinyl]propyl}-3-O-acetylursolamide
C56H82N6O7     ÏàËÆ¶È:54.3%
Bioorganic & Medicinal Chemistry          2008          16          771-782
Pharmacomodulation on the 3-acetylursolic acid skeleton: Design, synthesis, and biological evaluation of novel N-{3-[4-(3-aminopropyl)piperazinyl]propyl}-3-O-acetylursolamide derivatives as antimalarial agents
Simone C.B. Gnoatto, Sophie Susplugas, Luciana Dalla Vechia, Thais B. Ferreira, Alexandra Dassonville-Klimpt, Karine R. Zimmer, Catherine Demailly, Sophie Da Nascimento, Jean Guillon, Philippe Grellier, Hugo Verli, Grace Gosmann, Pascal Sonnet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
210 .     N-{3-[(4-(3-(4-Nitrobenzyl)amino)propyl)piperazi-nyl]propyl}-3-O-acetyl-ursolamide
C49H77N5O5     ÏàËÆ¶È:54.3%
Bioorganic & Medicinal Chemistry          2008          16          771-782
Pharmacomodulation on the 3-acetylursolic acid skeleton: Design, synthesis, and biological evaluation of novel N-{3-[4-(3-aminopropyl)piperazinyl]propyl}-3-O-acetylursolamide derivatives as antimalarial agents
Simone C.B. Gnoatto, Sophie Susplugas, Luciana Dalla Vechia, Thais B. Ferreira, Alexandra Dassonville-Klimpt, Karine R. Zimmer, Catherine Demailly, Sophie Da Nascimento, Jean Guillon, Philippe Grellier, Hugo Verli, Grace Gosmann, Pascal Sonnet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
211 .     (8'Z,11'R)-5-(11'-Hydroxy-octadec-8'-enyl)-2-phenylamine-1,3,4-oxadiazole
    ÏàËÆ¶È:54.3%
Bioorganic & Medicinal Chemistry Letters          2010          20          1933-1938
Synthesis, characterization, and in vitro antimicrobial activities of 5-alkenyl/hydroxyalkenyl-2-phenylamine-1,3,4-oxadiazoles and thiadiazoles
Nida N. Farshori, Mudasir R. Banday, Anis Ahmad, Asad U. Khan, Abdul Rauf
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
212 .     Calotropterpenylester
C42H82O2     ÏàËÆ¶È:54.3%
Pharmazie          2001          56          175-177
Norditerpenic ester and pentacyclic triterpenoids from root bark of Calotropis procera (Ait) R. Br.
S.H. Ansari - M. Ali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
213 .     24-Iodo-3¦Â-tetrahydropyranyloxychol-5-ene
    ÏàËÆ¶È:54.3%
Bioorganic & Medicinal Chemistry          1997          5          1893-1901
The design, synthesis and transmembrane transport studies of a biomimetic sterol-based ion channel
Anthony D. Pechulis, Richele J. Thompson, John P. Fojtik, Herbert M. Schwartz, Carol A. Lisek, Leah L. Frye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
214 .     3-O-(N-Nonyl)malonamoyl-12¦Â-acetoxy-3¦Á,25-dihy-droxy-(20S,24R)-epoxydammarane
C44H75NO7     ÏàËÆ¶È:54.3%
Bioorganic & Medicinal Chemistry          2010          18          2964-2975
Papyriferic acid derivatives as reversal agents of multidrug resistance in cancer cells
Juan Xiong, Masatoshi Taniguchi, Yoshiki Kashiwada, Michiko Sekiya, Takashi Yamagishi, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
215 .     Cheilocline B
C45H62O4     ÏàËÆ¶È:54.3%
Tetrahedron          2005          61          429-436
Cheiloclines A¨CI. First examples of octacyclic sesquiterpene-triterpene hetero-Diels¨CAlder adducts
Dulce Mesa-Siverio, Haydee Ch¨¢vez, Ana Est¨¦vez-Braun, ¨¢ngel G. Ravelo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
216 .     Cheilocline I
C45H62O4     ÏàËÆ¶È:54.3%
Tetrahedron          2005          61          429-436
Cheiloclines A¨CI. First examples of octacyclic sesquiterpene-triterpene hetero-Diels¨CAlder adducts
Dulce Mesa-Siverio, Haydee Ch¨¢vez, Ana Est¨¦vez-Braun, ¨¢ngel G. Ravelo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
217 .     3¦Â-butoxy-23,24-bisnorchol-5-en-22-yl-(N-3-methoxycarbonylpropyl)-amine
C31H51NO4     ÏàËÆ¶È:54.3%
Bioorganic & Medicinal Chemistry          2009          17          5950-5961
SAR studies on azasterols as potential anti-trypanosomal and anti-leishmanial agents
Federica Gigante, Marcel Kaiser, Reto Brun, Ian H. Gilbert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
218 .     32,33,34-trimethyl-bacteriohopan-16-ene 3-O-¦Â-D-glucopyranoside
C44H76O6     ÏàËÆ¶È:54.3%
Journal of Ethnopharmacology          2011          135          78-87
Chemical constituents from the stem bark of Symplocos paniculata Thunb. with antimicrobial, analgesic and anti-inflammatory activities
Ruchi Badoni Semwal, Deepak Kumar Semwal, Ravindra Semwal, Randhir Singh, Mohan Singh Maniyari Rawat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
219 .     N-{3-[4-(3-aminopropyl)piperazinopropyl]terbutylcarbamate}-3-O-acetylursolamide
C47H80N4O5     ÏàËÆ¶È:54.3%
European Journal of Medicinal Chemistry          2008          43          1865-1877
Evaluation of ursolic acid isolated from Ilex paraguariensis and derivatives on aromatase inhibition
Simone C.B. Gnoatto, Alexandra Dassonville-Klimpt, Sophie Da Nascimento, Philippe Gal¨¦ra, Karim Boumediene, Grace Gosmann, Pascal Sonnet, Safa Moslemi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
220 .     compound 23d(less polar isomer)
C35H49BrO5     ÏàËÆ¶È:54.3%
Journal of Medicinal Chemistry          2012          55          10662-10673
Bile Acid-Based 1,2,4-Trioxanes: Synthesis and Antimalarial Assessment1
Chandan Singh, , Mohammad Hassam, Ved Prakash Verma, Ajit Shanker Singh, Niraj Krishna Naikade, Sunil K. Puri, Prakas R. Maulik, and Ruchir Kant
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
221 .     compound 24d(less polar isomer)
C33H45BrO4     ÏàËÆ¶È:54.3%
Journal of Medicinal Chemistry          2012          55          10662-10673
Bile Acid-Based 1,2,4-Trioxanes: Synthesis and Antimalarial Assessment1
Chandan Singh, , Mohammad Hassam, Ved Prakash Verma, Ajit Shanker Singh, Niraj Krishna Naikade, Sunil K. Puri, Prakas R. Maulik, and Ruchir Kant
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
222 .     (R)-2-((R)-1-acetoxy-17-{(1S,2R)-2-[(1S,20S,21S)-20-(tert-butyldimethylsilanyloxy)-1,21-dimethyl-nonatriacontyl]cyclopropyl}heptadecyl)hexacosnoic acid methyl ester
C96H190O5Si     ÏàËÆ¶È:54.3%
Tetrahedron          2013          69          6285-6296
The synthesis of methoxy and keto mycolic acids containing methyl-trans-cyclopropanes
Gani Koza, Maged Muzael, Richard R. Schubert-Rowles, Cornelia Theunissen, Juma'a R. Al Dulayymi, Mark S. Baird
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
223 .     (24R)-29-O-acetyl-cholest-5,16-dien-22-one-3¦Â-ol
C31H48O4     ÏàËÆ¶È:54.3%
New Journal of Chemistry          2013          37          3647-3661
Synthesis of analogues of linckoside B, a new neuritogenic steroid glycoside
Qingchao Liu, Yue Yu, Peng Wang and Yingxia Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
224 .     10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl 2-(1-(((tert-butoxycarbonyl)amino)methyl)cyclohexyl)acetate
C41H69NO4     ÏàËÆ¶È:54.3%
Bioorganic & Medicinal Chemistry          2014          22          1479-1486
Gabapentin hybrid peptides and bioconjugates
Iryna O. Lebedyeva, David A. Ostrov, John Neubert, Peter J. Steel, Kunal Patel, Sean M. Sileno, Kevin Goncalves, Mohamed A. Ibrahim, Khalid A. Alamry, Alan R. Katritzky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
225 .     Benzyl 3¦Á-acetoxy-7¦Á,12¦Á-bis(decanoyloxy)-5¦Â-cholate
C53H84O8     ÏàËÆ¶È:54.3%
Steroids          2011          76          1082-1097
Investigation of new acyloxy derivatives of cholic acid and their esters as drug absorption modifiers
Lech Mr¨®zek, Lenka Dvoř¨¢kov¨¢, Zuzana Mandelov¨¢, Lucie R¨¢rov¨¢, Anna Řez¨¢čov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
226 .     3¦Á,7¦Á,12¦Á-Tris(decanoyloxy)-5¦Â-cholic acid
C54H94O8     ÏàËÆ¶È:54.3%
Steroids          2011          76          1082-1097
Investigation of new acyloxy derivatives of cholic acid and their esters as drug absorption modifiers
Lech Mr¨®zek, Lenka Dvoř¨¢kov¨¢, Zuzana Mandelov¨¢, Lucie R¨¢rov¨¢, Anna Řez¨¢čov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
227 .     3¦Á,7¦Á,12¦Á-Tris(hexadecanoyloxy)-5¦Â-cholic acid
C72H130O8     ÏàËÆ¶È:54.3%
Steroids          2011          76          1082-1097
Investigation of new acyloxy derivatives of cholic acid and their esters as drug absorption modifiers
Lech Mr¨®zek, Lenka Dvoř¨¢kov¨¢, Zuzana Mandelov¨¢, Lucie R¨¢rov¨¢, Anna Řez¨¢čov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
228 .     5,6-epoxy-solasodine-3¦Â-acteate
C29H45NO4     ÏàËÆ¶È:54.3%
Steroids          2012          77          1069-1074
Application of hypoiodite-mediated aminyl radical cyclization to synthesis of solasodine acetate
Yi Kou, Myong Chul Koag, Young Cheun, Aram Shin, Seongmin Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
229 .     Neomaclafungin I
C46H80O10     ÏàËÆ¶È:54.3%
Journal of Natural Products          2012          75          1974-1982
Neomaclafungins A¨CI: Oligomycin-Class Macrolides from a Marine-Derived Actinomycete
Seizo Sato, Fumie Iwata, Shoichi Yamada, and Masashi Katayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
230 .     Klainedoxasterol
C79H146O7     ÏàËÆ¶È:54.3%
Fitoterapia          2013          86          108-114
Lanostane-type triterpenoid and steroid from the stem bark of Klainedoxa gabonensis
Eric Ren¨¦ Sieliatchom Nkanwen, Anar Sahib Gojayev, Hippolyte Kamdem Wabo, Jean Jules Kezetas Bankeu, Muhammad Choudhary Iqbal, Akif Alakbar Guliyev, Pierre Tane
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
231 .     Dimer E
C41H66O6     ÏàËÆ¶È:54.3%
Molecules          2013          18          5936-5953
Dimeric Labdane Diterpenes: Synthesis and Antiproliferative Effects
Mariano Walter Pertino, Cristina Theoduloz, Marco Bast¨ªas and Guillermo Schmeda-Hirschmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
232 .     Dimer F
C42H68O6     ÏàËÆ¶È:54.3%
Molecules          2013          18          5936-5953
Dimeric Labdane Diterpenes: Synthesis and Antiproliferative Effects
Mariano Walter Pertino, Cristina Theoduloz, Marco Bast¨ªas and Guillermo Schmeda-Hirschmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
233 .     Dimer I
C44H69N3O6     ÏàËÆ¶È:54.3%
Molecules          2013          18          5936-5953
Dimeric Labdane Diterpenes: Synthesis and Antiproliferative Effects
Mariano Walter Pertino, Cristina Theoduloz, Marco Bast¨ªas and Guillermo Schmeda-Hirschmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
234 .     Dimer J
C45H71N3O6     ÏàËÆ¶È:54.3%
Molecules          2013          18          5936-5953
Dimeric Labdane Diterpenes: Synthesis and Antiproliferative Effects
Mariano Walter Pertino, Cristina Theoduloz, Marco Bast¨ªas and Guillermo Schmeda-Hirschmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
235 .     Dimer K
C45H71N3O6     ÏàËÆ¶È:54.3%
Molecules          2013          18          5936-5953
Dimeric Labdane Diterpenes: Synthesis and Antiproliferative Effects
Mariano Walter Pertino, Cristina Theoduloz, Marco Bast¨ªas and Guillermo Schmeda-Hirschmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
236 .     Dimer L
C46H73N3O6     ÏàËÆ¶È:54.3%
Molecules          2013          18          5936-5953
Dimeric Labdane Diterpenes: Synthesis and Antiproliferative Effects
Mariano Walter Pertino, Cristina Theoduloz, Marco Bast¨ªas and Guillermo Schmeda-Hirschmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
237 .     22-Dehydroclerosterol 3¦Â-O-¦Â-D-(6'-O-margaroyl)-glucopyranoside
    ÏàËÆ¶È:54.3%
Steroids          2013          78          711-716
New cytotoxic steroids from the leaves of Clerodendrum trichotomum
Rui-Lan Xu, Rui Wang, Lan Ding, Yan-Ping Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
238 .     N,N-dimethyl-(3¦Â-acetate-ergosta-5,7,12-triene)-N-decylammonium bromide
C42H71NO2Br2     ÏàËÆ¶È:54.3%
Molecules          2013          18          14961-14976
Synthesis, Spectroscopic and Semiempirical Studies of New Quaternary Alkylammonium Conjugates of Sterols
Bogumił Brycki, Hanna Koenig, Iwona Kowalczyk and Tomasz Pospieszny
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
239 .     N,N-dimethyl-(3¦Â-acetate-ergosta-5,7,12-triene)-N-dodecylammonium bromide
C44H75NO3     ÏàËÆ¶È:54.3%
Molecules          2013          18          14961-14976
Synthesis, Spectroscopic and Semiempirical Studies of New Quaternary Alkylammonium Conjugates of Sterols
Bogumił Brycki, Hanna Koenig, Iwona Kowalczyk and Tomasz Pospieszny
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
240 .     compound 7
    ÏàËÆ¶È:54.1%
Chemical & Pharmaceutical Bulletin          1992          40          1773-1778
Marine Natural Products. XXX. Two New 3-Keto-4-methylene Steroids, Theonellasterone and Conicasterone, and a Diels-Alder Type Dimeric Steroid Bistheonellasterone, from the Okinawan Marine Sponge Theonella swinhoei
Motomasa KOBAYASHI,Kazuyoshi KAWAZOE,Taketo KATORI and Isao KITAGAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
241 .     iristectorene F
    ÏàËÆ¶È:54.1%
Phytochemistry          1994          36          425-431
Iristectorenes A and C-G, monocyclic triterpene esters from Iris tectorum
Katsura Seki, Toshiya Tomihari, Kazuo Haga, Ryohei Kaneko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
242 .     malevamide A
C54H80N8O10     ÏàËÆ¶È:54%
Journal of Natural Products          2000          63          461-467
Malevamides A-C, New Depsipeptides from the Marine Cyanobacterium Symploca laete-viridis
F. David Horgen, Wesley Y. Yoshida, and Paul J. Scheuer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
243 .     compound 6
    ÏàËÆ¶È:53.1%
Chemical & Pharmaceutical Bulletin          1992          40          1773-1778
Marine Natural Products. XXX. Two New 3-Keto-4-methylene Steroids, Theonellasterone and Conicasterone, and a Diels-Alder Type Dimeric Steroid Bistheonellasterone, from the Okinawan Marine Sponge Theonella swinhoei
Motomasa KOBAYASHI,Kazuyoshi KAWAZOE,Taketo KATORI and Isao KITAGAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
244 .     14-benzoyldelphonine-8-palmitate
C47H73NO9     ÏàËÆ¶È:53.1%
Journal of Natural Products          1994          Vol 57          963
Long-Chain Fatty Acid Esters of Some Norditerpenoid Alkaloids
Yili Bai, Haridutt K. Desai, S. William Pelletier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
245 .     endo-and exo-14-[18'-methoxycarbonyl-13',14',15',16'-tetranorlabda-8'(17')-en-12'-yl]-15-oxa-3-azoniatricyclo[9.4.0.(11,12)]hexadeca-10,13-diene bromides
C30H44BrNO3     ÏàËÆ¶È:53.1%
Russian Journal of Organic Chemistry          2005          41          1145-1157
Synthetic Transformations of Higher Terpenoids: X. Intramolecular Cyclization of N-Allyl- and N-Propargyl-16-dialkylammoniomethyl-12-furfuryl-13,14,15,16-tetranorlabdanoid Bromides
Yu.V. Kharitonov, E.E. Shults, M.M. Shakirov and G.A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
246 .     3,4-O-isopropylidene-2-O-[1-methyl-1-(cholest-5-en-3¦Â-yl-sulfanyl)-ethyl]-1-(cholest-5-en-3¦Â-yl-sulfanyl)-¦Â-D-galactopyranose
C66H110O5S2     ÏàËÆ¶È:53.1%
Steroids          2014          82          60-67
Electrochemical synthesis of glycoconjugates from activated sterol derivatives
Aneta M. Tomkiel, Jan Kowalski, Jolanta Płoszy¨½ska, Leszek Siergiejczyk, Zenon Łotowski, Andrzej Sobkowiak, Jacek W. Morzycki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
247 .     3¦Â-hydroxy-35-(cyclohexyl-5'-propan-7'-one)-33-ethyl-34-methyl-bactereohopane
C47H82O2     ÏàËÆ¶È:53.1%
Chinese Chemical Letters          2011          22          81-84
A novel bacteriohopanoid from Celtis australis L. bark
Ruchi Badoni, Deepak Kumar Semwal, Prabhakar P. Badoni, Sudhir Kumar Kothiyal, Usha Rawat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
248 .     compound 26
C45H74N8O7     ÏàËÆ¶È:53.1%
Tetrahedron          2014          70          3297-3305
The CuI-catalyzed alkyne¨Cazide cycloaddition as direct conjugation/cyclization method of peptides to steroids
Radell Echemend¨ªa, Odette Concepci¨®n, Fidel E. Morales, M¨¢rcio W. Paixão, Daniel G. Rivera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
249 .     compound 1
    ÏàËÆ¶È:53.0%
Chemistry of Natural Compounds          2005          41          007-010
SYNTHESIS OF TRITERPENE DERIVATIVES OF D-GLUCOSAMINE -MODIFIED ANALOGS OF GLYCYRRHIZIC ACID
R. M. Kondratenko, S. R. Mustafina, L. A. Baltina,F. Z. Galin, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
250 .     14-benzoyldelphonine-8-stearate
C49H77NO9     ÏàËÆ¶È:53.0%
Journal of Natural Products          1994          Vol 57          963
Long-Chain Fatty Acid Esters of Some Norditerpenoid Alkaloids
Yili Bai, Haridutt K. Desai, S. William Pelletier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
251 .     28-O-¦Á-L-Rhamnopyranosylbetulin 3¦Â-O-¦Á-L-rhamnopyranoside
C42H70O10     ÏàËÆ¶È:52.1%
Journal of Natural Products          2009          72          72-81
Synthesis and Cytotoxicity of Bidesmosidic Betulin and Betulinic Acid Saponins
Charles Gauthier,Jean Legault,Serge Lavoie, Simon Rondeau, Samuel Tremblay, and Andr¨¦ Pichette
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
252 .     24-methylenecycloartanyl 2'E,4'E-decadienoate
C41H66O2     ÏàËÆ¶È:52.1%
Journal of Natural Products          2009          72          1258-1264
Diterpenoids and Triterpenoids from Euphorbia retusa
Hamada Haba, Catherine Lavaud, Abdulmagid Alabdul Magid, and Mohammed Benkhaled
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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