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| 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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²éѯ½á¹û£º¹²²éµ½424¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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. 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(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 ̼Æ×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. 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(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. 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(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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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