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| 13C NMR (126 MHz, CDCl3) ¦Ä14.82,15.84,16.51,19.62,20.93,21.47,26.06,26.84,29.07,29.35,30.35,32.09,33.31,33.43,33.51,33.78,34.06,36.92,39.85,40.56,41.49,42.61,47.28,47.90,50.45,54.89,133.48,136.61,180.26 |
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²éѯ½á¹û£º¹²²éµ½10032¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . moronic acid ÏàËÆ¶È:93.3% Journal of Natural Products 2004 67 986-989 Cytotoxic Triterpenoids from Acridocarpus vivy from the Madagascar Rain Forest Shugeng Cao, Rebecca Clare Guza, James S. Miller, Rabodo Andriantsiferana, Vincent E. Rasamison, and David G. I. Kingston Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . moronic acid ÏàËÆ¶È:93.3% Journal of Natural Products 2001 64 1278-1281 Anti-AIDS Agents. 48.1 Anti-HIV Activity of Moronic Acid Derivatives and the New Melliferone-Related Triterpenoid Isolated from Brazilian Propolis Junko Ito,Fang-Rong Chang, Hui-Kang Wang, Yong Kun Park, Masaharu Ikegaki, Nicole Kilgore,and Kuo-Hsiung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . moronic acid C30H46O3 ÏàËÆ¶È:93.3% Planta Medica 2001 67 443-446 Cytotoxic Activity of Moronic Acid and Identification of the New Triterpene 3,4-seco-Olean-18-ene-3,28-dioic Acid from Phoradendron reichenbachianum Mar¨ªa Yolanda Rios, David Salinas, Mar¨ªa Luisa Villarreal Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . moronic acid C30H46O3 ÏàËÆ¶È:93.3% Phytochemistry 1995 38 1275-1278 Terpenoids, alkaloids and coumarins from Boronia inornata and Boronia gracilipes Monira Ahsan, James A. Armstrong, Alexander I. Gray, Peter G. Waterman Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . moronic acid C30H46O3 ÏàËÆ¶È:93.3% Chinese Traditional and Herbal Drugs 1996 27 451-453 Studies on the Chemical Constituents of Taishan Yanfumu(Rhus taishanensis) Ma Tianbo; Liu Sizhen; Liu Chuanling; et al Ma Tianbo; (Department of Materia Medica; Shandong University of Traditional Chinese Medicine; Jinan); Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . acridocarpusic acid A C30H46O4 ÏàËÆ¶È:90% Journal of Natural Products 2004 67 986-989 Cytotoxic Triterpenoids from Acridocarpus vivy from the Madagascar Rain Forest Shugeng Cao, Rebecca Clare Guza, James S. Miller, Rabodo Andriantsiferana, Vincent E. Rasamison, and David G. I. Kingston Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Moronic acid methyl ester C31H48O3 ÏàËÆ¶È:90% Phytochemistry 1983 22 1828-1830 3-oxo-6¦Â-hydroxyolean-18-en-28-oic acid from orthopterygium huancuy Antonio G. Gonz¨¢lez, Jos¨¦ Amaro, Braulio M. Fraga, Javier G. Luis Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . acridocarpusic acid D C30H47O2 ÏàËÆ¶È:83.3% Journal of Natural Products 2004 67 986-989 Cytotoxic Triterpenoids from Acridocarpus vivy from the Madagascar Rain Forest Shugeng Cao, Rebecca Clare Guza, James S. Miller, Rabodo Andriantsiferana, Vincent E. Rasamison, and David G. I. Kingston Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3,4-seco-olean-18-ene-3,28-dioic acid C30H48O4 ÏàËÆ¶È:83.3% Planta Medica 2001 67 443-446 Cytotoxic Activity of Moronic Acid and Identification of the New Triterpene 3,4-seco-Olean-18-ene-3,28-dioic Acid from Phoradendron reichenbachianum Mar¨ªa Yolanda Rios, David Salinas, Mar¨ªa Luisa Villarreal Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Moronic acid ÏàËÆ¶È:83.3% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . acridocarpusic acid C C30H44O4 ÏàËÆ¶È:80% Journal of Natural Products 2004 67 986-989 Cytotoxic Triterpenoids from Acridocarpus vivy from the Madagascar Rain Forest Shugeng Cao, Rebecca Clare Guza, James S. Miller, Rabodo Andriantsiferana, Vincent E. Rasamison, and David G. I. Kingston Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3¦Â-hydroxy-3-deoxymoronic acid ÏàËÆ¶È:80% Journal of Natural Products 2001 64 1278-1281 Anti-AIDS Agents. 48.1 Anti-HIV Activity of Moronic Acid Derivatives and the New Melliferone-Related Triterpenoid Isolated from Brazilian Propolis Junko Ito,Fang-Rong Chang, Hui-Kang Wang, Yong Kun Park, Masaharu Ikegaki, Nicole Kilgore,and Kuo-Hsiung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 20,28-dihydroxylupane-3-one ÏàËÆ¶È:80% Phytochemistry 1998 48 863-866 Triterpenes from Rhus taitensis Aysen Y¨¹r¨¹ker, Jimmy Orjala, Otto Sticher, Topul Rali Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . morolic acid ÏàËÆ¶È:80% Journal of the Chinese Chemical Society 2000 47 555-560 The Chemical Constituents from the Heartwood of Eucalyptus citriodora Ching-Kuo Lee* and Ming-Huey Chang Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3-Oxoplatanic acid ÏàËÆ¶È:79.3% Phytochemistry 1998 49 709-717 Bioactive polar triterpenoids from Melilotus messanensis Francisco A. Mac¨ªas, Ana M. Simonet, Juan Carlos G. Galindo, Pedro C. Pacheco, Jose A. S¨¢nchez Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . acridocarpusic acid B C32H48O5 ÏàËÆ¶È:78.1% Journal of Natural Products 2004 67 986-989 Cytotoxic Triterpenoids from Acridocarpus vivy from the Madagascar Rain Forest Shugeng Cao, Rebecca Clare Guza, James S. Miller, Rabodo Andriantsiferana, Vincent E. Rasamison, and David G. I. Kingston Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . methyl 3¦Á-hydroxyolean-18-en-28-oate C31H40O3 ÏàËÆ¶È:77.4% Phytochemistry 1995 39 99-103 Terpenoids from the liverworts Symphyogyna brasiliensis and unidentified Frullania species Motoo Tori, Mamiko Aoki, Katsuyuki Nakashima, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Germanicone ÏàËÆ¶È:76.6% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Morolic acid acetate ÏàËÆ¶È:76.6% Acta Botanica Sinica 2004 46 371-374 Triterpenoids from Erythrophleum fordii LI Nan, YU Fang, YU Shi-Shan Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 16¦Â-acetoxyolean-18-en-3-one C32H50O3 ÏàËÆ¶È:76.6% Journal of Natural Products 1989 Vol 52 567 ¦¤18 Oleane Triterpenes from Schaefferia cuneifolia Antonio G. Gonzalez, J. J. Mendoza, A. G. Ravelo, J. G. Luis, X. A. Dominguez Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . moronic aldehyde C30H46O2 ÏàËÆ¶È:76.6% Phytochemistry 1995 38 1275-1278 Terpenoids, alkaloids and coumarins from Boronia inornata and Boronia gracilipes Monira Ahsan, James A. Armstrong, Alexander I. Gray, Peter G. Waterman Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 3,21-dioxo-olean-18-en-oic acid ÏàËÆ¶È:76.6% Organic letters 2001 3 4047-4049 The First Naturally Occurring Tie2 Kinase Inhibitor Bing-Nan Zhou, Randall K. Johnson, Michael R. Mattern, Paul W. Fisher, and David G. I. Kingston Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . morolic acid C30H48O3 ÏàËÆ¶È:76.6% Chinese Journal of Natural Medicines 2010 8 414-418 Triterpenoids from the Fruits of Forsythia suspensa XUE Jiao; XIE Li; LIU Bao-Rui; YU Li-Xia Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 17,24-epoxy-25-hydroxy-3-oxobaccharan-21-oic acid C30H48O5 ÏàËÆ¶È:76.6% The Journal of Organic Chemistry 2004 69 3350-3358 Silvestrol and Episilvestrol, Potential Anticancer Rocaglate Derivatives from Aglaia silvestris Bang Yeon Hwang, Bao-Ning Su, Heebyung Chai, Qiuwen Mi, Leonardus B. S. Kardono, Johar J. Afriastini, Soedarsono Riswan, Bernard D. Santarsiero, Andrew D. Mesecar, Robert Wild, Craig R. Fairchild, Gregory D. Vite, William C. Rose, Norman R. Farnsworth, Ge Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . Messagenic acid H C29H44O5 ÏàËÆ¶È:75.8% Phytochemistry 1998 49 709-717 Bioactive polar triterpenoids from Melilotus messanensis Francisco A. Mac¨ªas, Ana M. Simonet, Juan Carlos G. Galindo, Pedro C. Pacheco, Jose A. S¨¢nchez Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 3-oxo-6¦Â-hydroxyolean-18-en-28-oic acid methyl ester C31H48O4 ÏàËÆ¶È:75.8% Phytochemistry 1983 22 1828-1830 3-oxo-6¦Â-hydroxyolean-18-en-28-oic acid from orthopterygium huancuy Antonio G. Gonz¨¢lez, Jos¨¦ Amaro, Braulio M. Fraga, Javier G. Luis Structure 13C NMR ̼Æ×Ä£Äâͼ |

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