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13C 500M CDCl3Êý¾ÝÈçÏ£º 16.29,17.38,18.59,21.49,22.32,23.40,23.58,25.34,25.74,28.43,30.64,31.04,32.57,32.93,33.42,33.85,36.95,37.14,37.54,42.65,43.48,44.86,45.61,48.37,61.65,69.69,75.82,128.29,169.39,200.34 лл |
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1 . 3¦Á-hydroxy-11-oxoolean-12-en-28-oic acid C30H46O4 ÏàËÆ¶È:86.6% Journal of Natural Products 2006 69 142-144 Lupane and Oleanane Triterpenoids from the Cones of Liquidamber styraciflua Yuko Fukuda, Takeshi Yamada, Shun-ich Wada, Kuniyoshi Sakai, Shunyo Matsunaga, and Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . krukovine A C30H46O3 ÏàËÆ¶È:86.6% Journal of Natural Products 1997 60 1174-1177 Partial Synthesis of Krukovines A and B, Triterpene Ketones Isolated from the Brazilian Medicinal Plant Maytenus krukovii Tadashi Honda, Heather J. Finlay, and Gordon W. Gribble Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . krukovine A C30H46O3 ÏàËÆ¶È:83.3% Journal of Natural Products 1996 59 1072-1075 Triterpenes from Brazilian Medicinal Plant ¡°Chuchuhuasi¡± (Maytenus krukovii) Osamu Shirota, Toshihiko Tamemura, Hiroshi Morita, Koichi Takeya, and Hideji Itokawa Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3,11-dioxoolean-12-en-28-yl acetate C32H48O4 ÏàËÆ¶È:81.2% Journal of Natural Products 1997 60 1174-1177 Partial Synthesis of Krukovines A and B, Triterpene Ketones Isolated from the Brazilian Medicinal Plant Maytenus krukovii Tadashi Honda, Heather J. Finlay, and Gordon W. Gribble Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3,11-dioxoolean-12-en-28-oic acid ÏàËÆ¶È:80% Journal of Natural Products 2006 69 142-144 Lupane and Oleanane Triterpenoids from the Cones of Liquidamber styraciflua Yuko Fukuda, Takeshi Yamada, Shun-ich Wada, Kuniyoshi Sakai, Shunyo Matsunaga, and Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 11-oxo-erythrodiol C30H48O3 ÏàËÆ¶È:80% Phytochemistry 1998 47 1101-1105 Oleanane-type triterpenes from Viburnum awabuki Masami Kagawa, Hiroyuki Minami, Mai Nakahara, Hironobu Takahashi, Shigeru Takaoka, Yoshiyasu Fukuyama Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 11-oxo-erythrodiol C30H48O3 ÏàËÆ¶È:80% Phytochemistry 1998 47 1337-1341 Oleanane-type triterpenes from Viburnum awabuki Masami Kagawa, Hiroyuki Minami, Mai Nakahara, Hironobu Takahashi, Shigeru Takaoka, Yoshiyasu Fukuyama Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 11-oxo-erythrodiol ÏàËÆ¶È:80% Archives of Pharmacal Research 2002 25 617-620 Pentacyclic triterpenoids fromllex macropoda Dae Keun Kim, II Yong Nam, Jin Wook Kim, Tae Yong Shin and Jong Pil Lim Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3¦Â,28-epoxydihydroxy-11-oxo-12-ene ÏàËÆ¶È:80% Journal of the Brazilian Chemical Society 2002 13 669-673 Fatty Acid Esters of Triterpenes from Erythroxylum passerinums Marizeth L. Barreiros, Jorge M. David, Pedro A. de P. Pereira, Maria L. S. Guedes and Juceni P. David Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3¦Â-acetoxy-12-oleanen-11-one ÏàËÆ¶È:78.1% China Journal of Chinese Materia Medica 2010 35 2708-2711 Chemical constituents of Indigofera pseudotinctoria WEN Erya; LIANG Hong Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 11-keto-¦Â-amyrenyl-acetate ÏàËÆ¶È:78.1% Lishizhen Medicine and Materia Medica Research 2011 22 1329-1330 The Chemical Constituents of Euphorbia cyathophora CHEN Lin; MU Shu-zhen; JIANG Chun-yong; GE Yong-hui; ZHANG Jian-xin; HAO Xiao-jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (3¦Á,18¦Â,20¦Â)-3-hydroxy-11-oxo-olean-12-en-29-oic acidmethyl ester ÏàËÆ¶È:77.4% Bioorganic & Medicinal Chemistry 2010 18 433-454 Synthesis of glycyrrhetinic acid derivatives for the treatment of metabolic diseases Igor Beseda, Laszlo Czollner, Priti S. Shah, Rupesh Khunt, Rawindra Gaware, Paul Kosma, Christian Stanetty, Maria Carmen del Ruiz-Ruiz, Hassan Amer, Kurt Mereiter, Thierry Da Cunha, Alex Odermatt, Dirk Claßen-Houben, Ulrich Jordis Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 11-oxo-3¦Â-hydroxy-olean-12-ene ÏàËÆ¶È:76.6% Chinese Pharmaceutical Journal 2005 40 900-902 Studies on chemical constituents of Sabia schumanniana LIANG Guang-yi, ZHOU Ying, CAO Pei-xue, XU Bi-xue Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (3¦Á,18¦Â,20¦Â)-11-oxo-3-trifluoromethylsulfonylamino-olean-12-en-29-oic acid ÏàËÆ¶È:76.6% Bioorganic & Medicinal Chemistry 2010 18 7522-7541 Synthesis of novel 3-amino and 29-hydroxamic acid derivatives of glycyrrhetinic acid as selective 11¦Â-hydroxysteroid dehydrogenase 2 inhibitors Christian Stanetty, Laszlo Czollner, Iris Koller, Priti Shah, Rawindra Gaware, Thierry Da Cunha, Alex Odermatt, Ulrich Jordis, Paul Kosma, Dirk Claßen-Houben Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (3¦Á,18¦Â,20¦Â)-3-(acetylamino)-11-oxo-olean-12-en-29-oicacid ÏàËÆ¶È:75% Bioorganic & Medicinal Chemistry 2010 18 7522-7541 Synthesis of novel 3-amino and 29-hydroxamic acid derivatives of glycyrrhetinic acid as selective 11¦Â-hydroxysteroid dehydrogenase 2 inhibitors Christian Stanetty, Laszlo Czollner, Iris Koller, Priti Shah, Rawindra Gaware, Thierry Da Cunha, Alex Odermatt, Ulrich Jordis, Paul Kosma, Dirk Claßen-Houben Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 3,11-dioxo-18¦Â-olean-12-en-28-oic acid ÏàËÆ¶È:74.1% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Methyl 11-oxo-olean-12-en-30-oate ÏàËÆ¶È:74.1% Zeitschrift f¨¹r Naturforschung B 2011 66 521-532 Synthesis and Antitumor Activity of Ring A-modified Glycyrrhetinic Acid Derivatives R. Csuk, S. Schwarz, B. Siewert, R. Kluge, and D. Ströhl Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (3¦Á,18¦Â,20¦Â)-N-hydroxy-N-methyl-11-oxo-3-[(trifluoro-methylsulfonyl)amino]-olean-12-en-29-amide ÏàËÆ¶È:74.1% Bioorganic & Medicinal Chemistry 2010 18 7522-7541 Synthesis of novel 3-amino and 29-hydroxamic acid derivatives of glycyrrhetinic acid as selective 11¦Â-hydroxysteroid dehydrogenase 2 inhibitors Christian Stanetty, Laszlo Czollner, Iris Koller, Priti Shah, Rawindra Gaware, Thierry Da Cunha, Alex Odermatt, Ulrich Jordis, Paul Kosma, Dirk Claßen-Houben Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (3¦Â,18¦Â,20¦Â)-3-acetoxy-N-methyl-N-methoxy-11-oxo-olean-12-en-29-amide ÏàËÆ¶È:73.5% Bioorganic & Medicinal Chemistry 2010 18 7522-7541 Synthesis of novel 3-amino and 29-hydroxamic acid derivatives of glycyrrhetinic acid as selective 11¦Â-hydroxysteroid dehydrogenase 2 inhibitors Christian Stanetty, Laszlo Czollner, Iris Koller, Priti Shah, Rawindra Gaware, Thierry Da Cunha, Alex Odermatt, Ulrich Jordis, Paul Kosma, Dirk Claßen-Houben Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . lantanone C32H48O5 ÏàËÆ¶È:73.3% Journal of Natural Products 2000 63 765-767 Nematicidal Constituents of the Aerial Parts of Lantana camara Sabira Begum,Aneela Wahab, Bina S. Siddiqui, and Fatima Qamar Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . krukovine C C30H46O4 ÏàËÆ¶È:73.3% Journal of Natural Products 1996 59 1072-1075 Triterpenes from Brazilian Medicinal Plant ¡°Chuchuhuasi¡± (Maytenus krukovii) Osamu Shirota, Toshihiko Tamemura, Hiroshi Morita, Koichi Takeya, and Hideji Itokawa Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . olean-1 2-ene-3¦Á,16¦Â-diol C30H50O2 ÏàËÆ¶È:73.3% Planta Medica 1989 55 44-47 New Hepatoprotective Triterpenes from Canarium album Masaharu Tamai, Naoharu Watanabe, Maywni Soineya,Hideaki Kondoh, Sadafumi Omura Zhang PeiLing, Rao Chang, and Chen Wei Ming Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 23-Oxoerythrodiol ÏàËÆ¶È:73.3% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 3¦Â-hydroxyolean-12-en-11-one ÏàËÆ¶È:73.3% Natural Product Sciences 1998 4 253-256 Oleanane Triterpenoids from Gordonia ceylanica Herath, H.M.T.B.; Athukoralage, P.S. Structure 13C NMR ̼Æ×Ä£Äâͼ |

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