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CMH-14-1 Pyr 15.8,16.1,17.8,20.5,21.2,21.4,22.0,24.5,25.5,27.0,32.4,33.8,34.8,36.5,37.3,39.9,41.8,41.9,42.3,45.6,46.8,47.4,47.7,48.4,55.5,63.5,68.0,73.1,75.4,125.0,129.9,136.7,144.9,168.3,216.7 |
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²éѯ½á¹û£º¹²²éµ½6277¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 22-O-angeloylcamelliagenin B C35H54O5 ÏàËÆ¶È:77.1% Chemical & Pharmaceutical Bulletin 1996 44 1899-1907 Bioactive Saponins and Glycosides. V. Acylated Polyhydroxyolean-12-ene Triterpene Oligoglycosides, Camelliasaponins A1, A2, B1, B2, C1, and C11, from the Seeds of Camellia japonica L. : Structures and Inhibitory Activity on Alcohol Absorption Masayuki YOSHIKAWA,Toshiyuki MURAKAMI,Satoshi YOSHIZUMI,Nobutoshi MURAKAMI,Johji YAMAHARA and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . aesculioside IIb C52H82O22 ÏàËÆ¶È:71.4% Phytochemistry 2006 67 784-794 Triterpenoid saponins from the fruits of Aesculus pavia Zhizhen Zhang, Shiyou Li, Shanmin Zhang, David Gorenstein Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . aesculioside IId C46H72O17 ÏàËÆ¶È:71.4% Phytochemistry 2006 67 784-794 Triterpenoid saponins from the fruits of Aesculus pavia Zhizhen Zhang, Shiyou Li, Shanmin Zhang, David Gorenstein Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 22-O-tigloylcamelliagenin B C35H54O5 ÏàËÆ¶È:71.4% Chemical & Pharmaceutical Bulletin 1996 44 1899-1907 Bioactive Saponins and Glycosides. V. Acylated Polyhydroxyolean-12-ene Triterpene Oligoglycosides, Camelliasaponins A1, A2, B1, B2, C1, and C2, from the Seeds of Camellia japonica L. : Structures and Inhibitory Activity on Alcohol Absorption Masayuki YOSHIKAWA,Toshiyuki MURAKAMI,Satoshi YOSHIZUMI,Nobutoshi MURAKAMI,Johji YAMAHARA and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 22-O-angeloylcamelliagenin C C35H54O6 ÏàËÆ¶È:71.4% Chemical & Pharmaceutical Bulletin 1996 44 1899-1907 Bioactive Saponins and Glycosides. V. Acylated Polyhydroxyolean-12-ene Triterpene Oligoglycosides, Camelliasaponins A1, A2, B1, B2, C1, and C3, from the Seeds of Camellia japonica L. : Structures and Inhibitory Activity on Alcohol Absorption Masayuki YOSHIKAWA,Toshiyuki MURAKAMI,Satoshi YOSHIZUMI,Nobutoshi MURAKAMI,Johji YAMAHARA and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 22¦Á-µ±¹éõ£»ù-ÓñÈï´¼ A1 ÏàËÆ¶È:71.4% Chinese Traditional and Herbal Drugs 2011 42 1936-1938 Chemical constituents in roots of Camellia oleifera TONG, Xiao-jing, CHEN, Zhong, LI, Xia, LI, Xiao-ran, XU, Qiong-ming, YANG, Shi-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . pictoside B C35H56O10 ÏàËÆ¶È:68.5% Chemical & Pharmaceutical Bulletin 2002 50(7) 900-903 Activity-Guided Isolation of Saponins from Kalopanax pictus with Anti-inflammatory Activity Da Wei LI,Eun Bang LEE,Sam Sik KANG, Jin Ee HYUN,and Wan Kyun WHANG Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . aesculioside IIa C52H82O22 ÏàËÆ¶È:68.5% Phytochemistry 2006 67 784-794 Triterpenoid saponins from the fruits of Aesculus pavia Zhizhen Zhang, Shiyou Li, Shanmin Zhang, David Gorenstein Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . argenteanone C C30H48O3 ÏàËÆ¶È:68.5% Journal of Natural Products 1997 60 81-85 Argenteanones C-E and Argenteanols B-E, Cytotoxic Cycloartanes from Aglaia argentea K. Mohamad, M.-T. Martin, E. Leroy, C. Temp¨ºte, T. S¨¦venet, K. Awang, and M. Païs Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 22-O-tigloylcamelliagenin C C35H54O6 ÏàËÆ¶È:68.5% Chemical & Pharmaceutical Bulletin 1996 44 1899-1907 Bioactive Saponins and Glycosides. V. Acylated Polyhydroxyolean-12-ene Triterpene Oligoglycosides, Camelliasaponins A1, A2, B1, B2, C1, and C4, from the Seeds of Camellia japonica L. : Structures and Inhibitory Activity on Alcohol Absorption Masayuki YOSHIKAWA,Toshiyuki MURAKAMI,Satoshi YOSHIZUMI,Nobutoshi MURAKAMI,Johji YAMAHARA and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 5 ÏàËÆ¶È:68.5% Chemical & Pharmaceutical Bulletin 1985 33 3176-3181 Studies on the Constituents of Hedera rhombea BEAN. III. On the Dammarane Triterpene Glycosides. (2) HARUHISA KIZU,MICHIYO KOSHIJIMA and TSUYOSHI TOMIMORI Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3-oxo-15¦Á,16¦Á,21¦Â,22¦Á,28-pentahydroxy-¦¤(12)-oleanane C30H48O6 ÏàËÆ¶È:68.5% Phytochemistry 1994 35 201-204 Polyoxygenated oleanane triterpenes from hydrocotyle ranunculoides Marina Della Greca, Antonio Fiorentino, Pietro Monaco, Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 21-angeloyl-24-hydroxy-R1-barrigeno 1 C35H56O8 ÏàËÆ¶È:68.5% Chinese Traditional and Herbal Drugs 2008 39 334-337 Chemical constituents in carpophore of Xanthoceras sorbifolia LI Wei; LI Xian Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 21-O-angeloyl-R1-barrigenol ÏàËÆ¶È:68.5% Journal of Shenyang Pharmaceutical University 2005 22 345-347 Chemical constituents of the carpohore of Xanthoceras sorbifolia Bunge LI Wei, LI Xian, LI Zhan-lin, ZHANG Peng, XU Jing, WANG Yi Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 2n ÏàËÆ¶È:68.5% Australian Journal of Chemistry 1989 42 243-257 A One- and Two-Dimensional 13C and 1H N.M.R. Study of Some Triterpenes of the Hopane, Stictane and Flavicene Groups AL Wilkins, J Bremer, J Ralph, PT Holland, KJ Ronaldson, PM Jager and PW Bird Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (23E)-coumaroylhederagenin C39H54O6 ÏàËÆ¶È:67.5% Journal of Natural Products 2004 67 91-93 Three New Oleanane-Type Triterpenes from Ludwigia octovalvis with Cytotoxic Activity against Two Human Cancer Cell Lines Chi-I Chang, Ching-Chuan Kuo, Jang-Yang Chang, and Yueh-Hsiung Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 11¦Â,21¦Â-dihydroxy-olean-12-ene-3-one C30H48O3 ÏàËÆ¶È:65.7% Phytochemistry 2008 69 1057-1064 21¦Â-Hydroxy-oleanane-type triterpenes from Hippocratea excelsa David C¨¢ceres-Castillo, Gonzalo J. Mena-Rej¨®n,Roberto Cedillo-Rivera, Leovigildo Quijano Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . aesculioside IIc C52H82O21 ÏàËÆ¶È:65.7% Phytochemistry 2006 67 784-794 Triterpenoid saponins from the fruits of Aesculus pavia Zhizhen Zhang, Shiyou Li, Shanmin Zhang, David Gorenstein Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 12-O-acetylbetulafolienediolone ÏàËÆ¶È:65.7% Chemical & Pharmaceutical Bulletin 1996 44 1033-1038 Chemical Evaluation of Betula Species in Japan. II. Constituents of Betula platyphylla var. japonica Hiroyuki FUCHINO,Soh KONISHI,Tetsuya SATOH,Akiko YAGI,Kohei SAITSU,Tatsuya TATSUMI and Nobutoshi TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 2 ÏàËÆ¶È:65.7% Chinese Chemical Letters 2006 17 211-214 A New Triterpenoid Spaonin Isolated from the Seeds of Aesculus assamica Griff Hong Wei LIU, Xin Sheng YAO, Nai Li WANG, Guo Ping CAI Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . soyasapogenol ÏàËÆ¶È:65.7% Journal of Chinese Pharmaceutical Sciences 2005 14 75-78 Chemical Constituents of Hedysarum gmelinii LIU Yi; MA Xiao-xia; CHEN Hu-biao; TU Guang-zhong; HE Jiu-ming; and ZHAO Yu-ying Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . Saniculagenin N C35H56O7 ÏàËÆ¶È:65.7% Journal of Natural Products 1997 60 1170-1173 Saniculoside N from Sanicula europaea L. Nazlı Arda, Nezhun Gören, Avni Kuru, Thitima Pengsuparp, John M. Pezzuto, Sheng-Xiang Qiu, and Geoffrey A. Cordell Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 21¦Â-µ±¹éõ£»ùÔÆßÒ¶ÔíÜÕÔª ÏàËÆ¶È:65.7% Chinese Traditional and Herbal Drugs 2003 34 970-973 Study on aescin metabolism in intestinal flora in vitro CHEN Ji yong; WU Li jun; TENG Hou lei; LIU Ke Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . compound 6 ÏàËÆ¶È:65.7% Chinese Traditional and Herbal Drugs 1999 30(5) 327-332 Studies on the Chemical Constituents of Japanese Buckeye Seed (Aesculus turbinata)¢ñ£®Isolation and Identification of Escins ¢ña and ¢ñb Zhao Jing and Yang Xiuwei Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 2¦Â,3¦Â,16¦Á-Trihydroxyl-24¦Á-al-olean-12-en-28-oic acid C30H46O6 ÏàËÆ¶È:65.7% Pharmazie 2004 59 882-884 Pentacyclic triterpenoids from Aster ageratoides var. pilosus Fu-Lin Yan, Ai-Xia Wang, and Zhong-Jian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . methyl 23-acetoxy-3¦Â-hydroxyiminoolean-12-en-28-oate C33H51NO5 ÏàËÆ¶È:65.7% The Journal of Organic Chemistry 2007 72 3500-3509 Remote Hydroxylation of Methyl Groups by Regioselective Cyclopalladation. Partial Synthesis of Hyptatic Acid-A Andr¨¦s Garc¨ªa-Granados, Pilar E. L¨®pez, Enrique Melguizo, Andr¨¦s Parra, and Yolanda Sime¨® Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . compound 11 C33H52O5 ÏàËÆ¶È:65.7% The Journal of Organic Chemistry 2007 72 3500-3509 Remote Hydroxylation of Methyl Groups by Regioselective Cyclopalladation. Partial Synthesis of Hyptatic Acid-A Andr¨¦s Garc¨ªa-Granados, Pilar E. L¨®pez, Enrique Melguizo, Andr¨¦s Parra, and Yolanda Sime¨® Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . compound A C39H60O7 ÏàËÆ¶È:65.7% Bulletin des Soci¨¦t¨¦s Chimiques Belges 1983 92 473-484 Triterpenoïdes de Harpullia Cupanioïdes Makoso Zeza Dimbi, Roger Warin, Cl¨¦ment Delaude, Robert Huls and Kapundu Mpuza Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 22-oxo-3¦Â,24-dihydroxyolean-12-ene ÏàËÆ¶È:65.7% Journal of Chinese Medicinal Materials 2012 35 1246-1250 Study on Triterpenoids from Wisteria sinensis LIU Jin-song, CHEN Ai-min, XU Ying-sheng, ZHANG Cong-er, WANG Gang Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . lantadene C ÏàËÆ¶È:65.7% Journal of the Indian Chemical Society 1999 76 723-726 New triterpenoids from Lantana camara:Isomerisation of the angeloyl moiety of lantadene A during catalytic hydrogenation S.B.Mahato,S.Sharma,B.Pramanik and O.P.Sharma Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 3(S)-acetoxy-3-methyl-1-cyano-19 ,28-epoxy-2,3-seco-2-nor-18¦ÁH-oleanane ÏàËÆ¶È:65.7% Chemistry of Natural Compounds 2014 49 1059-1066 Synthesis of A-Pentacyclic Triterpene ¦Á,¦Â-Alkenenitriles A. V. Pereslavtseva, I. A. Tolmacheva, P. A. Slepukhin, O. S. El¡¯tsov, I. I. Kucherov, V. F. Eremin, V. V. Grishko Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . N-5-[2-(2-Aminoethylamino)ethyl]-1,2,8,8,15,19,19-heptamethyl-18-oxopentacyclo[12.8.0.02,11.05,10.015,20]-docos-11-en-5-carboxamide C34H57N3O2 ÏàËÆ¶È:65.7% Chemistry of Natural Compounds 2011 47 68-72 Synthesis of new betulonic and oleanonic acid amides G. V. Giniyatullina, O. B. Kazakova, E. V. Salimova and G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . 21¦Â-hydroxy-¦Â-amyrenone ÏàËÆ¶È:65.7% Natural Product Research and Development 2013 25 1070-1073 Chemical Constituents of Biogas Residues LIU Ding-cai, ZHU Hong-guang, XU Jian-feng* Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . 3,28-Dioxo-28-(6-aminohexylamino)olean-12-ene C36H60N2O2 ÏàËÆ¶È:65.7% Russian Journal of Bioorganic Chemistry 2013 39 329-337 Synthesis of aminopropylamino derivatives of betulinic and oleanolic acids G. V. Giniyatullina, O. B. Kazakova, N. I. Medvedeva, I. V. Sorokina, N. A. Zhukova, T. G. Tolstikova, G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . 2¦Â,3¦Â,16¦Á-trihydroxyl-23¦Á-formyl-12-en-28-oic acid C30H46O6 ÏàËÆ¶È:65.7% Journal of Xingxiang Medical College 2010 27 140-143 Terpenoid constituents extract from Aster ageratoides var. polosus and antibacterial activity ZHAO Xiao-jie, GUO Lan-qing Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . 21¦Â, 22¦Á-O-diangeloyl prosapogenin C40H62O8 ÏàËÆ¶È:65% Phytochemistry 2002 59 825-832 Triterpenoid saponins and acylated prosapogenins from Harpullia austro-caledonica Laurence Voutquenne, C¨¦cile Kokougan, Catherine Lavaud,Isabelle Pouny, Marc Litaudon Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . 21,22-diangeloyl-24-hydroxy-R1-barrigenol C40H62O9 ÏàËÆ¶È:65% Planta Medica 2005 71 1068-1070 Two New Triterpenes from the Husks of Xanthoceras sorbifolia Zhan-Lin Li , Xian Li , Lin-Hao Li , Ning Li , Ming Yu , Da-Li Meng Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . (23Z)-Feruloylhederagenin C40H56O7 ÏàËÆ¶È:65% Journal of Asian Natural Products Research 2007 9 67-72 Oleanane-type triterpenes from Ludwigia octovalvis C.-I. CHANG and Y.-H. KUO Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . 1¦Â-angeloyl-3¦Â,15¦Á,16¦Á,28-tetrahydroxy-22¦Á-(2-methylbutanoyloxy)-olean-12-en-23-al C40H62O9 ÏàËÆ¶È:65% Helvetica Chimica Acta 2013 96 1126-1133 Triterpenoids from the Roots of Camellia oleifera C.Abel and Their Cytotoxic Activities Shou-Li Wang, Zhong Chen, Xiao-Jing Tong, Yan-Li Liu, Xia Li, Qiong-Ming Xu, Xiao-Ran Li and Shi-Lin Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . 21¦Â-angeloyloxy-3¦Â,16¦Á,28-trihydroxy-22¦Á-(2-methylbutanoyloxy)olean-12-en-23-al C40H62O8 ÏàËÆ¶È:65% Helvetica Chimica Acta 2013 96 1126-1133 Triterpenoids from the Roots of Camellia oleifera C.Abel and Their Cytotoxic Activities Shou-Li Wang, Zhong Chen, Xiao-Jing Tong, Yan-Li Liu, Xia Li, Qiong-Ming Xu, Xiao-Ran Li and Shi-Lin Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . 21¦Â-µ±¹éõ£»ù-22¦Á-ÒÒõ£»ùÔÆßÒ¶ÔíÜÕÔª ÏàËÆ¶È:64.8% Chinese Traditional and Herbal Drugs 2003 34 970-973 Study on aescin metabolism in intestinal flora in vitro CHEN Ji yong; WU Li jun; TENG Hou lei; LIU Ke Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . soyasapogenol B 3-O-¦Â-D-glucopyranuronoside ÏàËÆ¶È:63.8% Chemistry of Natural Compounds 1995 31 596-599 TRITERPENE GLYCOSIDES OF Sophora japonica SEEDS V. I. Grishkovets and L. A. Gorbacheva Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . compound 7 C40H58O5 ÏàËÆ¶È:63.8% Tetrahedron 1993 49 4275-4282 Toxicols A-C and toxiusol - new bioactive hexaprenoid hydroquinones from Toxiclona toxius Sara Isaacs, Amnon Hizi, Yoel Kashman Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . 3-O-(¦Â-D-glucuronopyranosyl)-soyasapogenol B C36H58O9 ÏàËÆ¶È:63.8% Zeitschrift f¨¹r Naturforschung C 2005 60 813-820 Bioactive Saponins from Astragalus suberi L. Growing in Yemen F. Abbas and R. Zayed Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . caraganin B C36H54O11 ÏàËÆ¶È:63.8% Journal of Natural Medicines 2012 66 Two new triterpenoid saponins from Caragana microphylla seeds Cheng-Jian Zheng • Gui-Lin Jin • Jing-Ping Zou •Yi-Ping Jiang • Pei-Xin Sun • Lu-Ping Qin Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . caraganin B C36H54O11 ÏàËÆ¶È:63.8% Journal of Natural Medicines 2013 67 190-195 Two new triterpenoid saponins from Caragana microphylla seeds Cheng-Jian Zheng, Gui-Lin Jin, Jing-Ping Zou, Yi-Ping Jiang¡ Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . Oleanolic acid 3-O-¦Á-D-mannopyranoside C36H58O8 ÏàËÆ¶È:63.8% Molecules 2011 16 1113-1128 Synthesis and Anti-Fungal Activity of Seven Oleanolic Acid Glycosides Hanqing Zhao, Guanghui Zong, Jianjun Zhang, Daoquan Wang and Xiaomei Liang Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . 3¦Â-[(¦Á-L-arabinopyranosyl)oxy]-23-oxo-olean-12-en-28-oic acid C35H54O8 ÏàËÆ¶È:62.8% Journal of Natural Products 2009 72 1155-1160 Triterpene Glycosides from the Underground Parts of Caulophyllum thalictroides Yukiko Matsuo, Kazuki Watanabe, and Yoshihiro Mimaki Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . sugikurojin G C35H54O2 ÏàËÆ¶È:62.8% Chemical & Pharmaceutical Bulletin 2006 54(3) 315-319 Three Abietane Diterpenes and Two Diterpenes Incorporated Sesquiterpenes from the Bark of Cryptomeria japonica Kazuko YOSHIKAWA, Toshinori TANAKA, Akemi UMEYAMA, and Shigenobu ARIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . 3¦Á,21¦Â-dihydroxy-olean-12-ene ÏàËÆ¶È:62.8% Phytochemistry 2008 69 1057-1064 21¦Â-Hydroxy-oleanane-type triterpenes from Hippocratea excelsa David C¨¢ceres-Castillo, Gonzalo J. Mena-Rej¨®n,Roberto Cedillo-Rivera, Leovigildo Quijano Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . 29-hydroxy-12-oleanene-3,22-dione C30H46O3 ÏàËÆ¶È:62.8% Journal of Natural Products 2008 71(11) 1829-1832 Triterpenoids and Aromatics from Derris laxiflora Hsi-Lin Chiu, Jyh-Horng Wu, Yu-Tang Tung, Tzong-Huei Lee, Shin-Chang Chien, and Yueh-Hsiung Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . 21¦Â-hydroxyolean-12-en-3-on C30H48O2 ÏàËÆ¶È:62.8% Journal of Natural Products 2007 70 863-865 Antigiardial Activity of Triterpenoids from Root Bark of Hippocratea excelsa Gonzalo J. Mena-Rej¨®n,Aida R. P¨¦rez-Espadas, Rosa E. Moo-Puc, Roberto Cedillo-Rivera,I. L. Bazzocchi,I. A. Jim¨¦nez-Diaz, and Leovigildo Quijano Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . 3¦Â-acetoxy-19¦Á-methoxy-20-taraxastene C33H54O3 ÏàËÆ¶È:62.8% Journal of Natural Products 2000 63 898-901 Taraxastane-Type Triterpenes from the Aerial Roots of Ficus microcarpa Y. M. Chiang and Y. H. Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ |

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