CyRhmU.jpeg
²é¿´: 520  |  »Ø¸´: 2

gyqqtbn01

гæ (³õÈëÎÄ̳)

[ÇóÖú] ΢Æ×ÇóÖú£¬Ð»Ð»ÒÑÓÐ2È˲ÎÓë

ë®´úÂÈ·Â
15.4,18.3,18.8,19.0,19.0,19.8,20.2,21.1,22.6,22.8,23.1,23.9,25.4,26.1,26.1,28.0,28.9,29.1,30.3,31.9,32.4,33.7,34.0,35.8,35.9,36.1,36.2,38.9,39.1,39.5,40.4,42.7,45.9,51.3,55.5,55.6,55.6,55.7,56.1,129.5,138.2
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

·çÐÐÕß007

ÖÁ×ðľ³æ (ÖøÃûдÊÖ)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
gyqqtbn01: ½ð±Ò+10 2015-04-14 10:03:29
²éѯ½á¹û£º¹²²éµ½1503¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     aglycone-II
    ÏàËÆ¶È:76.7%
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
2 .     Acutifloric acid
    ÏàËÆ¶È:70.7%
Phytochemistry          1995          40          607-609
Frutoic acid, a dimeric kaurane diterpene from Xylopia frutescens
Jacqueline A. Takahashi, Maria Am¨¦lia D. Boaventura, Joaquim de Carvalho Bayma, Ala¨ªde B. Oliveira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     24-Ethylcholesterol-acetate
    ÏàËÆ¶È:70.7%
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
4 .     ¦Â-sitosterol and stigmasterol
    ÏàËÆ¶È:70.7%
The Chinese Pharmaceutical Journal          2000          52          261-273
Studies on Anti-inflammatory Constituents of Leucas Mollissima WALL. var. Chinensis Benth
¹Åؑͥ(Chen-Ting Ku), ê?„ÙÖÇ(Sheng-Chih Chen), ÍõÀ^ƽ(Jih-Pyang Wang), …ǽðžI(Jin-Bin Wu), ¹ù„ÙÖú(Sheng-Chu Kuo)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     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:70.7%
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
6 .     4-(2'-Phenylethyl)-5-N-cyclohexylcarboxamido-4-aza-5¦Á-cholestan-3-one
C41H64N2O2     ÏàËÆ¶È:68.2%
Steroids          2008          73          1270-1276
Synthesis of 4-azasteroids by an intramolecular Ugi reaction
Fernando Alonso, Sof¨ªa L. Acebedo, Andrea C. Bruttomesso, Javier A. Ram¨ªrez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3¦Â-[(2E,4E)-6-oxo-decadienoyloxy]-olean-12-ene
    ÏàËÆ¶È:68.2%
China Journal of Chinese Materia Medica          2008          33          405-408
Studies on phenolic compounds from Stellera chamaejasme
FENG Bao, GONG Xiaojie, SHI Liying, JIAN Ge, PEI Yue-hu, WANG Yong-qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 23c(less polar isomer)
C35H49ClO5     ÏàËÆ¶È:68.2%
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
9 .     compound 23d(less polar isomer)
C35H49BrO5     ÏàËÆ¶È:68.2%
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
10 .     compound 1d
C41H62O4     ÏàËÆ¶È:68.2%
Journal of the Indian Chemical Society          1991          68          88-91
Arundinol,A New Triterpene from the Orchid Arundina bambusifolia
P.L.MAJUMDER and SABARI GHOSAL
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (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:66.6%
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
12 .     32,33,34-trimethyl-bacteriohopan-16-ene 3-O-¦Â-D-glucopyranoside
C44H76O6     ÏàËÆ¶È:65.9%
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
13 .     (3b,20R)-20- hydroxylanost-25-en-3-yl palmitate
C46H82O3     ÏàËÆ¶È:65.8%
Helvetica Chimica Acta          2006          Vol. 89          558
Terpenoids from Eupatorium fortunei TURCZ
Hai-Xia Jiang, Ya Li, Jing Pan, and Kun Gao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     3¦Â-[(2E,4E)-5-oxo-decadienoyloxy]-olean-12-ene
C40H62O3     ÏàËÆ¶È:65.8%
Chemical & Pharmaceutical Bulletin          2006          54(6)          920-921
Pentacyclic Triterpenoids from Leaves of Excoecaria agallocha
Jian-Hua ZOU,Jungui DAI,Xiaoguang CHEN,and Jing-Quan YUAN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     3'¦Á-[¦Â-sitosteryl-3¦Â-oxy]dihydronepetalactone
C39H64O3     ÏàËÆ¶È:65.8%
Journal of Natural Products          2000          63          888-890
Constituents of Nepeta caesarea
G¨¹la¦Ãtı Top¦Ãu, Gamze Kökdil, and Sabiha Manav Yal¦Ãı
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Z-L-Met-l-Ala-O-cholesterol
C43H66N2O5S     ÏàËÆ¶È:65.8%
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
17 .     4-Butyl-5-N-cyclohexylcarboxamido-4-aza-5¦Á-cholestan-3-one
C37H64N2O2     ÏàËÆ¶È:65.8%
Steroids          2008          73          1270-1276
Synthesis of 4-azasteroids by an intramolecular Ugi reaction
Fernando Alonso, Sof¨ªa L. Acebedo, Andrea C. Bruttomesso, Javier A. Ram¨ªrez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     moldenin
C40H64O3     ÏàËÆ¶È:65.8%
Phytochemistry          1999          50          443-447
A bis-labdenic diterpene from Moldenhawera nutans
Juceni P. David, Jorge M. David, Shu-Wei Yang, Geoffrey A. Cordell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     Frutoic acid
C40H60O4     ÏàËÆ¶È:65.8%
Phytochemistry          1995          40          607-609
Frutoic acid, a dimeric kaurane diterpene from Xylopia frutescens
Jacqueline A. Takahashi, Maria Am¨¦lia D. Boaventura, Joaquim de Carvalho Bayma, Ala¨ªde B. Oliveira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     Mixture of 7-oxostigmast-5-en-3¦Â-yl oleate and palmitate
    ÏàËÆ¶È:65.8%
Phytochemistry          1992          31          4263-4274
Cycloartanes and other terpenoids and phenylpropanoids from Monocyclanthus vignei
Hans Achenbach, Dieter Frey
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     compound 9
    ÏàËÆ¶È:65.8%
Tetrahedron Letters          2000          41          3875-3878
Synthesis of 3¦Â-(5¡ä-D-ribityl)cholestane, a putative biological precursor for fossil 3-alkylsteranes
Tore Duvold, Michel Rohmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     3¦Â-[N-(N',N'-di(2''-hydroxyethyl)-2'-aminoethyl)-N-(N-glycine(N-(2-aminoethyl)amide))carbamoyl] cholesterol
    ÏàËÆ¶È:65.8%
Bioorganic & Medicinal Chemistry          2010          18          330-342
Solid phase synthesis of novel asymmetric hydrophilic head cholesterol-based cationic lipids with potential DNA delivery
Widchaya Radchatawedchakoon, Ramida Watanapokasin, Aungkana Krajarng, Boon-ek Yingyongnarongkul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     ¦Á,¦Â-amyrin
    ÏàËÆ¶È:65.8%
Natural Product Research and Development          2002          14(3)          1-6
STUDIES ON THE CHEMICAL CONSTITUENTS OF THE FLOWER OF CAMPSIS GRANDIFLORA (THUNB.)K.SCHUM.AND ITS CONTRACEPTIVE EFFECT
ZHAO Qian; LIAO Mao chuan GUO Ji xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     Methyl (3¦Â)-3-({6-[(tert-butoxycarbonyl)amino]hexanoyl}-oxy)-11-oxoolean-12-en-30-oate
C42H67NO7     ÏàËÆ¶È:65.8%
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
25 .     6¦Â-hydroxysitostan-3¦Á-(4'-phenyl)thiosemicarbamide
C36H55N3OS     ÏàËÆ¶È:65.8%
Steroids          2014          87          99-107
Synthesis and antiproliferative activity of some steroidal thiosemicarbazones, semicarbazones and hydrozones
Chunfang Gan, Jianguo Cui, Shaoyang Su, Qifu Lin, Linyi Jia, Lianghua Fan, Yanmin Huang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     (1R,3aR,4RS,5S,7aR)-1-((R)-1,5-dimethylhexyl)-5-(2,6-dimethylmorpholine-4-yl)-3a,7a-dimethyl-octahydroinden-4-ol
    ÏàËÆ¶È:65.2%
Bioorganic & Medicinal Chemistry          2013          21          1925-1943
Stereoselective synthesis of a new class of potent and selective inhibitors of human ¦¤8,7-sterol isomerase
Mathias König, Christoph M¨¹ller, Franz Bracher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     3¦Â-Acetoxy-7¦Â-tert-butyldimethylsilyloxystigma-5-ene
C37H66O3Si     ÏàËÆ¶È:64.4%
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 .     ¦Â-sitosteryl-3-O-¦Â-D-glucopyranoside-2'-O-palmitate
C51H90O7     ÏàËÆ¶È:64.2%
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
29 .     7¦Â-Hydroxycholesteryl-9,10-dihydroxystearate
C45H80O5     ÏàËÆ¶È:64.2%
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
30 .     24,26-cyclo-5¦Á-cholest-(22E)-en-3¦Â-ol 4',8',12'-trimethyltridecanoate
C43H74O2     ÏàËÆ¶È:64.2%
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
31 .     7,13E-labdadien-15-yl malonic acid diester; ent-3,13E-clerodadien-15-yl-malonic acid diester
    ÏàËÆ¶È:64.2%
Phytochemistry          1990          29          2223-2228
Terpenoid compounds from Parentucellia latifolia
J.G. Urones,I.S. Marcos,I. Cubillo,N.Martin Garrido,P. Basabe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     ¦Â-sitosterol-3-O-¦Â-D-glucoside-6'-O-eicosanate
    ÏàËÆ¶È:64.2%
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
33 .     ¦Â-sitosteryl-3-O-¦Â-D-glucopyr-anoside-2'-O-palmitate
C51H90O7     ÏàËÆ¶È:64.2%
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
34 .     Sitosteryl oleate
C47H82O2     ÏàËÆ¶È:63.6%
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
35 .     ¦Â-sitosteryl-D-glucoside-6'-palmitate
C51H90O7     ÏàËÆ¶È:63.6%
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
½Å̤ʵµØ£¬·ÜÁ¦Ò»²«£¬Ô¹¬ÕÛ¹ð
2Â¥2014-12-04 13:27:21
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

nkx1979

ľ³æ (ÕýʽдÊÖ)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
²éѯ½á¹û£º¹²²éµ½1503¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     aglycone-II
    ÏàËÆ¶È:76.7%
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
2 .     Acutifloric acid
    ÏàËÆ¶È:70.7%
Phytochemistry          1995          40          607-609
Frutoic acid, a dimeric kaurane diterpene from Xylopia frutescens
Jacqueline A. Takahashi, Maria Am¨¦lia D. Boaventura, Joaquim de Carvalho Bayma, Ala¨ªde B. Oliveira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     24-Ethylcholesterol-acetate
    ÏàËÆ¶È:70.7%
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
4 .     ¦Â-sitosterol and stigmasterol
    ÏàËÆ¶È:70.7%
The Chinese Pharmaceutical Journal          2000          52          261-273
Studies on Anti-inflammatory Constituents of Leucas Mollissima WALL. var. Chinensis Benth
¹Åؑͥ(Chen-Ting Ku), ê?„ÙÖÇ(Sheng-Chih Chen), ÍõÀ^ƽ(Jih-Pyang Wang), …ǽðžI(Jin-Bin Wu), ¹ù„ÙÖú(Sheng-Chu Kuo)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     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:70.7%
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
6 .     4-(2'-Phenylethyl)-5-N-cyclohexylcarboxamido-4-aza-5¦Á-cholestan-3-one
C41H64N2O2     ÏàËÆ¶È:68.2%
Steroids          2008          73          1270-1276
Synthesis of 4-azasteroids by an intramolecular Ugi reaction
Fernando Alonso, Sof¨ªa L. Acebedo, Andrea C. Bruttomesso, Javier A. Ram¨ªrez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3¦Â-[(2E,4E)-6-oxo-decadienoyloxy]-olean-12-ene
    ÏàËÆ¶È:68.2%
China Journal of Chinese Materia Medica          2008          33          405-408
Studies on phenolic compounds from Stellera chamaejasme
FENG Bao, GONG Xiaojie, SHI Liying, JIAN Ge, PEI Yue-hu, WANG Yong-qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 23c(less polar isomer)
C35H49ClO5     ÏàËÆ¶È:68.2%
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
9 .     compound 23d(less polar isomer)
C35H49BrO5     ÏàËÆ¶È:68.2%
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
10 .     compound 1d
C41H62O4     ÏàËÆ¶È:68.2%
Journal of the Indian Chemical Society          1991          68          88-91
Arundinol,A New Triterpene from the Orchid Arundina bambusifolia
P.L.MAJUMDER and SABARI GHOSAL
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (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:66.6%
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
12 .     32,33,34-trimethyl-bacteriohopan-16-ene 3-O-¦Â-D-glucopyranoside
C44H76O6     ÏàËÆ¶È:65.9%
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
13 .     (3b,20R)-20- hydroxylanost-25-en-3-yl palmitate
C46H82O3     ÏàËÆ¶È:65.8%
Helvetica Chimica Acta          2006          Vol. 89          558
Terpenoids from Eupatorium fortunei TURCZ
Hai-Xia Jiang, Ya Li, Jing Pan, and Kun Gao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     3¦Â-[(2E,4E)-5-oxo-decadienoyloxy]-olean-12-ene
C40H62O3     ÏàËÆ¶È:65.8%
Chemical & Pharmaceutical Bulletin          2006          54(6)          920-921
Pentacyclic Triterpenoids from Leaves of Excoecaria agallocha
Jian-Hua ZOU,Jungui DAI,Xiaoguang CHEN,and Jing-Quan YUAN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     3'¦Á-[¦Â-sitosteryl-3¦Â-oxy]dihydronepetalactone
C39H64O3     ÏàËÆ¶È:65.8%
Journal of Natural Products          2000          63          888-890
Constituents of Nepeta caesarea
G¨¹la¦Ãtı Top¦Ãu, Gamze Kökdil, and Sabiha Manav Yal¦Ãı
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Z-L-Met-l-Ala-O-cholesterol
C43H66N2O5S     ÏàËÆ¶È:65.8%
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
17 .     4-Butyl-5-N-cyclohexylcarboxamido-4-aza-5¦Á-cholestan-3-one
C37H64N2O2     ÏàËÆ¶È:65.8%
Steroids          2008          73          1270-1276
Synthesis of 4-azasteroids by an intramolecular Ugi reaction
Fernando Alonso, Sof¨ªa L. Acebedo, Andrea C. Bruttomesso, Javier A. Ram¨ªrez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     moldenin
C40H64O3     ÏàËÆ¶È:65.8%
Phytochemistry          1999          50          443-447
A bis-labdenic diterpene from Moldenhawera nutans
Juceni P. David, Jorge M. David, Shu-Wei Yang, Geoffrey A. Cordell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     Frutoic acid
C40H60O4     ÏàËÆ¶È:65.8%
Phytochemistry          1995          40          607-609
Frutoic acid, a dimeric kaurane diterpene from Xylopia frutescens
Jacqueline A. Takahashi, Maria Am¨¦lia D. Boaventura, Joaquim de Carvalho Bayma, Ala¨ªde B. Oliveira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     Mixture of 7-oxostigmast-5-en-3¦Â-yl oleate and palmitate
    ÏàËÆ¶È:65.8%
Phytochemistry          1992          31          4263-4274
Cycloartanes and other terpenoids and phenylpropanoids from Monocyclanthus vignei
Hans Achenbach, Dieter Frey
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     compound 9
    ÏàËÆ¶È:65.8%
Tetrahedron Letters          2000          41          3875-3878
Synthesis of 3¦Â-(5¡ä-D-ribityl)cholestane, a putative biological precursor for fossil 3-alkylsteranes
Tore Duvold, Michel Rohmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     3¦Â-[N-(N',N'-di(2''-hydroxyethyl)-2'-aminoethyl)-N-(N-glycine(N-(2-aminoethyl)amide))carbamoyl] cholesterol
    ÏàËÆ¶È:65.8%
Bioorganic & Medicinal Chemistry          2010          18          330-342
Solid phase synthesis of novel asymmetric hydrophilic head cholesterol-based cationic lipids with potential DNA delivery
Widchaya Radchatawedchakoon, Ramida Watanapokasin, Aungkana Krajarng, Boon-ek Yingyongnarongkul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     ¦Á,¦Â-amyrin
    ÏàËÆ¶È:65.8%
Natural Product Research and Development          2002          14(3)          1-6
STUDIES ON THE CHEMICAL CONSTITUENTS OF THE FLOWER OF CAMPSIS GRANDIFLORA (THUNB.)K.SCHUM.AND ITS CONTRACEPTIVE EFFECT
ZHAO Qian; LIAO Mao chuan GUO Ji xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     Methyl (3¦Â)-3-({6-[(tert-butoxycarbonyl)amino]hexanoyl}-oxy)-11-oxoolean-12-en-30-oate
C42H67NO7     ÏàËÆ¶È:65.8%
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
25 .     6¦Â-hydroxysitostan-3¦Á-(4'-phenyl)thiosemicarbamide
C36H55N3OS     ÏàËÆ¶È:65.8%
Steroids          2014          87          99-107
Synthesis and antiproliferative activity of some steroidal thiosemicarbazones, semicarbazones and hydrozones
Chunfang Gan, Jianguo Cui, Shaoyang Su, Qifu Lin, Linyi Jia, Lianghua Fan, Yanmin Huang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     (1R,3aR,4RS,5S,7aR)-1-((R)-1,5-dimethylhexyl)-5-(2,6-dimethylmorpholine-4-yl)-3a,7a-dimethyl-octahydroinden-4-ol
    ÏàËÆ¶È:65.2%
Bioorganic & Medicinal Chemistry          2013          21          1925-1943
Stereoselective synthesis of a new class of potent and selective inhibitors of human ¦¤8,7-sterol isomerase
Mathias König, Christoph M¨¹ller, Franz Bracher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     3¦Â-Acetoxy-7¦Â-tert-butyldimethylsilyloxystigma-5-ene
C37H66O3Si     ÏàËÆ¶È:64.4%
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 .     ¦Â-sitosteryl-3-O-¦Â-D-glucopyranoside-2'-O-palmitate
C51H90O7     ÏàËÆ¶È:64.2%
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
29 .     7¦Â-Hydroxycholesteryl-9,10-dihydroxystearate
C45H80O5     ÏàËÆ¶È:64.2%
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
30 .     24,26-cyclo-5¦Á-cholest-(22E)-en-3¦Â-ol 4',8',12'-trimethyltridecanoate
C43H74O2     ÏàËÆ¶È:64.2%
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
31 .     7,13E-labdadien-15-yl malonic acid diester; ent-3,13E-clerodadien-15-yl-malonic acid diester
    ÏàËÆ¶È:64.2%
Phytochemistry          1990          29          2223-2228
Terpenoid compounds from Parentucellia latifolia
J.G. Urones,I.S. Marcos,I. Cubillo,N.Martin Garrido,P. Basabe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     ¦Â-sitosterol-3-O-¦Â-D-glucoside-6'-O-eicosanate
    ÏàËÆ¶È:64.2%
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
33 .     ¦Â-sitosteryl-3-O-¦Â-D-glucopyr-anoside-2'-O-palmitate
C51H90O7     ÏàËÆ¶È:64.2%
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
34 .     Sitosteryl oleate
C47H82O2     ÏàËÆ¶È:63.6%
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
35 .     ¦Â-sitosteryl-D-glucoside-6'-palmitate
C51H90O7     ÏàËÆ¶È:63.6%
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
ÌìµÀ³êÇÚ
3Â¥2014-12-04 14:50:17
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ gyqqtbn01 µÄÖ÷Ìâ¸üÐÂ
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û