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²éѯ½á¹û£º¹²²éµ½222¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (20S,24R)3¦Â,20,21¦Â,25-tetrahydroxy-21,24-cyclodammarane C30H52O4 ÏàËÆ¶È:70% Chinese Chemical Letters 2011 22 1461-1464 Two new dammarane-type sapogenins from Gynostemma pentaphyllum Xia Li,Jia Qing Cao,Lin Shi,Yu Qing Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Abiesatrine I C31H54O3 ÏàËÆ¶È:67.7% Organic & Biomolecular Chemistry 2010 8 2609-2616 Abiesatrines A¨CJ: anti-inflammatory and antitumor triterpenoids from Abies georgei Orr Xian-Wen Yang, Su-Mei Li, Liang Wu, Yong-Li Li, Lin Feng, Yun-Heng Shen, Jun-Mian Tian, Jian Tang, Ning Wang, Yonghong Liu and Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . sodwanone E ÏàËÆ¶È:66.6% Journal of Natural Products 1997 60 700-703 Sodwanones K, L, and M; New Triterpenes from the Marine Sponge Axinella weltneri Amira Rudi, Maurice Aknin, Emile M. Gaydou, and Yoel Kashman Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Aglaiabbreviatin D C30H48O2 ÏàËÆ¶È:66.6% Journal of Natural Products 2010 73 2042-2046 Triterpenoids from Aglaia abbreviata and Their Cytotoxic Activities Feng Zhang, Jun-Song Wang, Yu-Cheng Gu, and Ling-Yi Kong Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 7 ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 1988 26 581-590 13C NMR assignment of dammarane triterpenes and dendropanoxide: Application of 2D long-range 13C[BOND]1H correlation spectra Motoo Tori, Reiko Matsuda, Masakazu Sono and Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Neoabiestrine H C30H52O4 ÏàËÆ¶È:66.6% Phytochemistry 2012 81 159-164 Cytotoxic triterpenoids from Abies recurvata Yong-Li Li, Yan-Xia Gao, Xian-Wen Yang, Hui-Zi Jin, Ji Ye, Luke Simmons, Ning Wang, Andre Steinmetz, Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Â-acetoxyl-isofouquierol C32H54O4 ÏàËÆ¶È:65.6% 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 8 . compound 12 ÏàËÆ¶È:65.6% Magnetic Resonance in Chemistry 1988 26 581-590 13C NMR assignment of dammarane triterpenes and dendropanoxide: Application of 2D long-range 13C[BOND]1H correlation spectra Motoo Tori, Reiko Matsuda, Masakazu Sono and Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . leucastrin A C31H54O2 ÏàËÆ¶È:64.5% Chemical & Pharmaceutical Bulletin 2006 54 1370-1379 Studies on Nepalese Crude Drugs. XXIX. Chemical Constituents of Dronapuspi, the Whole Herb of Leucas cephalotes SPRENG. Yukinori Miyaichi, Akiko Segawa and Tsuyoshi Tomimori Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Combretanone E C31H50O3 ÏàËÆ¶È:64.5% Journal of Natural Products 2011 74 249-255 Cycloartane Triterpenes Isolated from Combretum quadrangulare in a Screening Program for Death-Receptor Expression Enhancing Activity Kazufumi Toume, Takafumi Nakazawa, Takashi Ohtsuki, Midori A. Arai, Takashi Koyano, Thaworn Kowithayakorn, and Masami Ishibashi Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Neoabiestrine I C31H54O4 ÏàËÆ¶È:64.5% Phytochemistry 2012 81 159-164 Cytotoxic triterpenoids from Abies recurvata Yong-Li Li, Yan-Xia Gao, Xian-Wen Yang, Hui-Zi Jin, Ji Ye, Luke Simmons, Ning Wang, Andre Steinmetz, Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . genipatriol C30H50O3 ÏàËÆ¶È:63.3% Journal of Natural Products 2003 66 398-400 Genipatriol, a New Cycloartane Triterpene from Genipa spruceana Chowdhury Faiz Hossain, Melissa R. Jacob, Alice M. Clark, Larry A. Walker, and Dale G. Nagle Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (23E)-23-dehydro-25-hydroxysunpollenol C30H52O3 ÏàËÆ¶È:63.3% Journal of Natural Products 2003 66 1476-1479 Sunpollenol and Five Other Rearranged 3,4-seco-Tirucallane-Type Triterpenoids from Sunflower Pollen and Their Inhibitory Effects on Epstein-Barr Virus Activation Motohiko Ukiya, Toshihiro Akihisa, Harukuni Tokuda, Kazuo Koike,Yumiko Kimura,Takeshi Asano,Shigeyasu Motohashi,Tamotsu Nikaido, and Hoyoku Nishino Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . sodwanone M C30H50O5 ÏàËÆ¶È:63.3% Journal of Natural Products 1997 60 700-703 Sodwanones K, L, and M; New Triterpenes from the Marine Sponge Axinella weltneri Amira Rudi, Maurice Aknin, Emile M. Gaydou, and Yoel Kashman Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Cyclosieversigenin ÏàËÆ¶È:63.3% Chemistry of Natural Compounds 1992 28 603-607 TRITERPENE GLYCOSIDES OF Astragalus AND THEIR GENINS XLIV. STRUCTURE OF CYCLOCARPOSIDES A AND C B. A. Imomnazarov and M. I. Isaev Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Cyclosieversigenin ÏàËÆ¶È:63.3% Chemistry of Natural Compounds 1992 28 461-463 TRITERPENE GLYCOSIDES OF Astragalus AND THEIR GENINS XLIII. CYCLOARALOSIDE B FROM Astragalus amarus M. I. Isaev Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Cyclosieversigenin ÏàËÆ¶È:63.3% Chemistry of Natural Compounds 1991 27 457-459 TRITERPENE GLYCOSIDES OF Astragalus AND THEIR GENINS XXXIX. CYCLOARALOSIDE D FROM Astragalus amarus M. I. Isaev Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 20S-dammarane-23-ene-3¦Â,20,25-triol ÏàËÆ¶È:63.3% Journal of Asian Natural Products Research 2008 10 33-37 Dammarane triterpenes from Ligustrum lucidum XIAO-HUA XU, NIAN-YUN YANG, SHI-HUI QIAN, NING XIE and JING-AO DUAN Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . fern-7-en-3¦Á-ol ÏàËÆ¶È:63.3% Chemical & Pharmaceutical Bulletin 1999 47 543-547 Fern Constituents : Six New Triterpenoid Alcohols from Adiantum capillus-veneris Takahisa NAKANE,Yoko ARAI,Kazuo MASUDA,Yuh ISHIZAKI,Hiroyuki AGETA and Kenji SHIOJIMA Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 3¦Á-hydroxytirucalla-7,24(25)-dien-6-oxo-21,16-olide C30H44O4 ÏàËÆ¶È:63.3% Journal of Natural Products 2010 73 693-697 Sterols and Terpenoids from Melia azedarach Qin-Gang Tan, Xiao-Ning Li, Hao Chen, Tao Feng, Xiang-Hai Cai and Xiao-Dong Luo Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 3-epibetulinate ÏàËÆ¶È:63.3% Journal of Natural Products 1984 Vol 47 673-676 Isoprenoids from the Leaves of Quercus suber Pietro Monaco, Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . sodwanone E C30H50O5 ÏàËÆ¶È:63.3% Journal of Natural Products 1994 Vol 57 1416 Sodwanones A-F, New Triterpenoids from the Marine Sponge Axinella weltneri Amira Rudi, Yoel Kashman, Yehuda Benayahu, Michael Schleyer Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . lup-20(29)-en-3-on-28-ol ÏàËÆ¶È:63.3% Acta Pharmaceutica Sinica 2005 Vol 40 935-939 Chemical constituents from the mangrove plant Ceriops tagal ZHANG Yan; DENG Zhi-wei; GAO Tian-xiang; FU Hong-zheng; LIN Wen-han Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . compound 348 ÏàËÆ¶È:63.3% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 8,26-cyclo-urs-21-en-3¦Â,20¦Â-diol C30H48O2 ÏàËÆ¶È:63.3% Zeitschrift f¨¹r Naturforschung B 2008 63b 1335-1338 Pentacyclic Triterpenes and Other Constituents from Ficus cordata (Moraceae) Herve M. P. Poumale, Rodrigue T. Kengap, Jean Claude Tchouankeu,Felix Keumedjio, Hartmut Laatsch, and Bonaventure T. Ngadjui Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . Mesendanin R C30H52O3 ÏàËÆ¶È:63.3% Helvetica Chimica Acta 2012 95 286-300 Triterpenoids from Melia toosendan Shi-Hui Dong, Xiu-Feng He, Lei Dong, Yan Wu, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . Elaeocarpucin F C30H48O5 ÏàËÆ¶È:63.3% Journal of Natural Products 2012 75 444−452 Isolation, Structure Elucidation, and Biological Evaluation of 16,23-Epoxycucurbitacin Constituents from Eleaocarpus chinensis Li Pan, Yeonjoong Yong,Ye Deng, Daniel D. Lantvit, Tran Ngoc Ninh, Heebyung Chai,Esperanza J. Carcache de Blanco, Djaja D. Soejarto, Steven M. Swanson, and A. Douglas Kinghorn Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . cycloastragenol ÏàËÆ¶È:63.3% Phytochemistry 1990 29 3271-3274 Cycloartane triterpene glycosides from EgyptianAstragalus species Nadia A. El-Sebakhy,Fathalla M. Harraz,Rokia M. Abdallah,Aya M. Asaad,F. Orsini,F. Pelizzoni,G. Sello,L. Verotta Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . Isofouquierone ÏàËÆ¶È:63.3% Phytochemistry 1985 24 2925-2928 Dammarane Triterpenes from the stem bark of Commiphora Dalzielii Peter G. Waterman, Stephen Ampofo Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . Isofouquierol ÏàËÆ¶È:63.3% 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 31 . 20R,24S-Epoxy-17-epi-cycloartan- 3¦Â,6¦Á,25-triol-16-one C30H48O5 ÏàËÆ¶È:63.3% Chemistry of Natural Compounds 2010 46 407-411 Triterpene glycosides from Astragalus and their genins. LXXXVII. Chemical transformation of cycloartanes. IX. Partial synthesis of cycloasalgenin I. M. Isaev, D. A. Iskenderov and M. I. Isaev Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . (20S)-dammar-23-ene-3¦Â,20,25-triol ÏàËÆ¶È:63.3% Chemistry & Biodiversity 2013 10 96-128 Chemical Constituents and Biological Activities of Plants from the Genus Ligustrum Bei-Bei Gao, Gai-Mei She and Dong-Mei She Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . 3¦Á-hydroxytirucalla-7,24(25)-dien-6-oxo-21,16-olide ÏàËÆ¶È:63.3% Natural Product Sciences 2013 19 342-346 A New Apotirucallane-type Triterpenoid from the Fruit of Melia azedarach Jin, Qinghao;Lee, Chul;Lee, Jin Woo;Lee, Moon-Soon;Lee, Mi Kyeong;Hwang, Bang Yeon Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . compound 5 ÏàËÆ¶È:63.3% Magnetic Resonance in Chemistry 1988 26 581-590 13C NMR assignment of dammarane triterpenes and dendropanoxide: Application of 2D long-range 13C[BOND]1H correlation spectra Motoo Tori, Reiko Matsuda, Masakazu Sono and Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . Lupeportlandol C30H50O ÏàËÆ¶È:63.3% Journal of the Brazilian Chemical Society 2004 15 742-747 Isoprenoid Compounds from Euphorbia portlandica. X-ray Structure of Lupeportlandol, a New Lupane Triterpene Ana M. Madureira, Maria Teresa Duarte, Maria F¨¢tima M. Piedade Jos¨¦ R. Ascenso and Maria-Jos¨¦ U. Ferreira Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . lithocarpic acid D C30H50O4 ÏàËÆ¶È:63.3% Journal of Natural Products 2014 77 1910-1920 Lithocarpic Acids A¨CN, 3,4-seco-Cycloartane Derivatives from the Cupules of Lithocarpus polystachyus Hongmin Wang, Ruonan Ning, Yu Shen, Zhenhua Chen, Jinlong Li, Rujun Zhang, Ying Leng, and Weimin Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . Kuguacin V C30H48O5 ÏàËÆ¶È:63.3% Planta Medica 2015 81 327−332 The Antigluconeogenic Activity of Cucurbitacins from Momordica charantia Jian-Chao Chen1, Clara Bik-San Lau2,3, Judy Yuet-Wa Chan2,3, Kwok-Pui Fung2,3, Ping-Chung Leung2,3, Jie-Qing Liu1,Lin Zhou1, Ming-Jin Xie4, Ming-Hua Qiu1 Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . cycloasgenin B ÏàËÆ¶È:63.3% Chemistry of Natural Compounds 2004 40 303-357 Triterpenoids from Astragalus Plants R. P. Mamedova, M. I. Isaev Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . 3¦Â-acetoxy-25-hydroxydammara-20,23-diene ÏàËÆ¶È:62.5% Planta Medica 2003 69 258-264 New Dihydrobenzofurans and Triterpenoids from Roots of Microglossa pyrifolia homas J.Schmidt,Meike R.Hildebrand,G¨¹nter Willuhn Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . cyclosieversigenin 6-Monoacetate ÏàËÆ¶È:62.5% Chemistry of Natural Compounds 2008 44 732-737 TRITERPENE GLYCOSIDES FROM Astragalus AND THEIR GENINS.LXXVIII. CHEMICAL TRANSFORMATION OF CYCLOARTANES.VI. PARTIAL SYNTHESIS OF CYCLOADSURGENINa I. M. Isaev, D. A. Iskenderov, and M. I. Isaev Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . nepehinol acetate ÏàËÆ¶È:62.5% Acta Pharmaceutica Sinica 1992 27 445-451 TRITERPENE CONSTITUENTS FROM EUPHORBIA NEMTOCYPHA HAND-MAZZ D Cao; YL Su; JS Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . (22S)-6-O-acetyl-21¦ÂH-hopane-3¦Â,6¦Â,22,29-tetrol C32H54O5 ÏàËÆ¶È:62.5% Natural Product Research 2004 18 379-385 (22S)-6-O-acetyl-21¦ÂH-hopane-3¦Â,6¦Â,22,29-tetrol from Oakmoss (Evrnia prunastri) Bjart Frode Lutnaes; Torger Bruun; Helge Kjøsen Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . 6-Monoacetate C34H54O7 ÏàËÆ¶È:62.5% Chemistry of Natural Compounds 2010 46 407-411 Triterpene glycosides from Astragalus and their genins. LXXXVII. Chemical transformation of cycloartanes. IX. Partial synthesis of cycloasalgenin I. M. Isaev, D. A. Iskenderov and M. I. Isaev Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . 3¦Â-acetoxy-25-hydroxydammara-20,23-diene C32H52O3 ÏàËÆ¶È:62.5% Journal of Tropical and Subtropical Botany 2014 22 413-418 Phenolic Derivatives and Steroids from Eupatorium adenophorum Spreng REN Hui, ZHANG Mei, ZHOU Zhong-yu, TAN Jian-wen, WAN Fang-hao Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . compound 4 ÏàËÆ¶È:62.5% Natural Medicines 1997 51 358-360 Studies on the Constituents of Astragalus membranaceus II. : Structure of Triterpenoidal Glycoside, Huangqiyenin D, from its Leaves Kuang Haixue,Zhang Ning, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . (3¦Â)-9,18-dihydroxyolean-12-en-3-yl acetate C32H52O4 ÏàËÆ¶È:62.5% Helvetica Chimica Acta 2013 96 533-537 Two New Pentacyclic Triterpenes from Abelmoschus esculentus Yonghui Zhou, Xin Jia, Jinmin Shi, Yinpeng Xu, Linlin Jing and Lu Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . 3-O-¦Â-D-(2'-OAc)-xylopyranosyl-6-O-¦Â-D-xylopyranosyl-3¦Â,6¦Á,16¦Â,24(R),25-pentahydroxycycloartane C42H70O14 ÏàËÆ¶È:62.5% Chemistry of Natural Compounds 2014 50 1012-1015 Cycloartane Glycosides from Euphorbia boissierana L. N. Gvazava, V. S. Kikoladze Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . 3-O-¦Â-D-(2'-OAc)-xylopyranosyl-6-O-¦Â-D-glucopyranosyl-3¦Â,6¦Á,16¦Â,24(R),25-pentahydroxycycloartane C43H72O15 ÏàËÆ¶È:62.5% Chemistry of Natural Compounds 2014 50 1012-1015 Cycloartane Glycosides from Euphorbia boissierana L. N. Gvazava, V. S. Kikoladze Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . foliasalaci A1 C31H54O2 ÏàËÆ¶È:61.2% Chemical & Pharmaceutical Bulletin 2008 56(7) 915-920 Hnew Triterpene Constituents, Foliasalacins A1¡ªA4, B1¡ªB3, and C, from the Leaves of Salacia chinensis Masayuki YOSHIKAWA,Yi ZHANG, Tao WANG, Seikou NAKAMURA, and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . foliasalaci A2 C31H54O2 ÏàËÆ¶È:61.2% Chemical & Pharmaceutical Bulletin 2008 56(7) 915-920 Hnew Triterpene Constituents, Foliasalacins A1¡ªA4, B1¡ªB3, and C, from the Leaves of Salacia chinensis Masayuki YOSHIKAWA,Yi ZHANG, Tao WANG, Seikou NAKAMURA, and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . igniaren D C31H52O2 ÏàËÆ¶È:61.2% Planta Medica 2009 75 1602-1607 Lanostanes from Phellinus igniarius and Their iNOS Inhibitory Activities Guei-JaneWang, Tung-Hu Tsai, Tun-Tschu Chang, Cheng-Jen Chou, Lie-Chwen Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . lanost-25-en-3¦Â-ol acetyl derivative ÏàËÆ¶È:61.2% Planta Medica 1999 65 478-479 A New Lanostane-Type Triterpenoid from Chamaesyce prostrata Susana Rojas, Martha Maclas, Perla Castañeda,Robert Bye, Edelmira Linares, and Rachel Mata Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . 24-methylene-lanosta-8-en-2¦Â,3¦Â,21-triol C31H52O3 ÏàËÆ¶È:61.2% Phytochemistry 1998 49 2053-2056 24-methylene tetracyclic triterpenes from Polyalthia lancilimba Y. P. Lue, Q. Mu, H. L. Zheng, C. M. Li Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . methyl senexdiolate ÏàËÆ¶È:61.2% Journal of Natural Products 1993 Vol 56 2170 The Absolute Stereochemistry of Senexdiolic Acid at C-22 Antonio G. Gonz¨¢lez, Teresa Siverio Exp¨®sito, Jaime Bermejo Barrera, Ana Garc¨ªa Castellano, Francisco J. Toledo Marante Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . isomotiol(fern-8-en-3¦Â-ol) acetate ÏàËÆ¶È:61.2% Korean Journal of Pharmacognosy 1985 16(3) 155-159 Studies on the Terpenoid constituents of Euphorbia supina Rafin Chung, Bo-Sup; Kim, Ha-Gyun Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . leucastrin A 3,20-ditrimethylsilyl ether derivative C37H61OSi2 ÏàËÆ¶È:61.2% Chemical & Pharmaceutical Bulletin 2006 54 1370-1379 Studies on Nepalese Crude Drugs. XXIX. Chemical Constituents of Dronapuspi, the Whole Herb of Leucas cephalotes SPRENG. Yukinori Miyaichi, Akiko Segawa and Tsuyoshi Tomimori Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . (20S,22R,25R)-5¦Á-spirostane-2¦Á,3¦Â,6¦Â-triol triacetate ÏàËÆ¶È:61.2% Phytochemistry 1988 27 2943-2945 Steroid sapogenins from Nothoscordum gramineum var. philippianum and Tristagma uniflorum M.C. Brunengo,O.L. Tombesi,D. Doller,E.G. Gros |

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