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kengkengsee: ½ð±Ò+5, ¡ïÓаïÖú 2013-12-07 09:13:40
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²éѯ½á¹û£º¹²²éµ½6360¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 21¦Â-Hydroxyserrat-14-en-3-one ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 1992 28 575-579 POLYFUNCTIONAL TRITERPENOIDS FROM THE BARK OF YEDDO SPRUCE G. F. Chernenko, I. Yu. Bagryanskaya,Yu. V. Gatilov, G. E. Sal'nikov,E. N. Shmidt, and V. I. Mamatyuk Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . serrat-14-en-3¦Â,21¦Â,24,29-tetraol C30H50O4 ÏàËÆ¶È:66.6% Natural Product Research 2004 18 453-459 Serratane-type Triterpenoids from Huperzia Serrata Hui Zhou; Yun-Sen Li; Xiao-Tian Tong; Hui-Qing Liu; Shan-Hao Jiang; Da-Yuan Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . euscaphic acid ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2007 32 496-500 Studies on chemical constituents in fruits of Eucalyptus globulus YANG Xiuwei, GUO Qingmei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 3,21-diepiserratenediol C30H50O2 ÏàËÆ¶È:66.6% Phytochemistry 1994 37 209-211 Serratenes from the stem bark of Picea Jezoensis carr. hondoensis Reiko Tanaka, Rie Tsuboi, Shunyo Matsunaga Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 24-(E)-3-oxo-dammara-6-¦Â-hydroxy-20,24-dien-26-al C30H46O3 ÏàËÆ¶È:66.6% Tetrahedron 1997 53 6465-6472 First examples of dammarane triterpenes isolated from Celastraceae Haydee Ch¨¢vez, Ana Est¨¦vez-Braun, Ángel G. Ravelo, Antonio G. Gonz¨¢lez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 3¦Â-Butynyloxy-5,6-epoxycholestane ÏàËÆ¶È:64.5% Steroids 2007 72 729-735 6E-Hydroximinosteroid homodimerization by cross-metathesis processes Miriam Rega, Carlos Jim¨¦nez, Jaime Rodr¨ªguez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 27-hydroxyambrein C30H54O3 ÏàËÆ¶È:63.3% Journal of Natural Products 2007 70 147-153 Chemical Transformation and Biological Activities of Ambrein, a Major Product of Ambergris from Physeter macrocephalus (Sperm Whale) Ya-Ching Shen,Shi-Yie Cheng,Yao-Haur Kuo,Tsong-Long Hwang,Michael Y. Chiang,and Ashraf Taha Khalil Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . yunganogenin C ÏàËÆ¶È:63.3% Chemical & Pharmaceutical Bulletin 1995 43 636-640 Five New Triterpene Glycosides from Wisteria branchybotrys (Leguminosae) Junei KINJO,Yoshie FUJISHIMA,Kazuyo SAINO,Rui-hua TIAN and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . compound 11b ÏàËÆ¶È:63.3% Chemical & Pharmaceutical Bulletin 1988 36 1646-1663 Tannins and Related Compounds. LXVII. : Isolation and Characterization of Castanopsinins A-H, Novel Ellagitannins Containing a Triterpenoid Glycoside Core, from Castanopsis cuspidata var. sieboldii NAKAI. (3) MASAYUKI AGETA,GEN-ICHIRO NONAKA and ITSUO NISHIOKA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . Soyasapogenol B C30H50O3 ÏàËÆ¶È:63.3% Journal of Asian Natural Products Research 2005 7 237-243 Three new isoprenylated flavonoids from the roots of Sophora flavescens PEI-LAN DING, AI-JUN HOU and DAO-FENG CHEN Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (22S,23S,24R)-24-methyl-22,23-epoxy-3¦Á,5-cyclo-5¦Á-cholestan-6¦Â-yl acetate ÏàËÆ¶È:63.3% Journal of Natural Products 1985 Vol 48 756-765 Starfish Saponins, Part 22. Asterosaponins from the Starfish Halityle regularis: A Novel 22,23-Epoxysteroidal Gylcoside Sulfate Raffaele Riccio, Maria Iorizzi, Olinda Squillace Greco, Luigi Minale, Maurice Debray, Jean Luis Menou Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . daucosterol ÏàËÆ¶È:63.3% Natural Product Sciences 2009 15 181-184 Phytochemical Constituents from the Seeds of Lithospermum erythrorhizon Park, Jun-Yeon; Lee, Sul-Lim; Han, Saem; Kim, Hye-Min; Lee, Jeong-Min; Ahn, Young-Hee; Lee, Sook-Young; Lee, Sang-Hyun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 21¦Â-Hydroxyserrat-14-en-3-one C30H48O2 ÏàËÆ¶È:63.3% Phytochemistry 1994 37 209-211 Serratenes from the stem bark of Picea Jezoensis carr. hondoensis Reiko Tanaka, Rie Tsuboi, Shunyo Matsunaga Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . olibanumol H C30H52O3 ÏàËÆ¶È:63.3% Chemical & Pharmaceutical Bulletin 2009 57 957-964 Absolute Stereostructures of Olibanumols A, B, C, H, I, and J from Olibanum, Gum-Resin of Boswellia carterii, and Inhibitors of Nitric Oxide Production in Lipopolysaccharide-Activated Mouse Peritoneal Macrophages Masayuki Yoshikawa, Toshio Morikawa, Hideo Oominami and Hisashi Matsuda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . uvaol ÏàËÆ¶È:63.3% Chinese Traditional and Herbal Drugs 2002 33 888-889 ËÄ´¨Áúµ¨µÄÈýÝÆ³É·Ö Nam joon-young,ÁõÏòǰ,ÕųÐìÇ,³Êç¼§,Àî¼Ãîç,½²ýä¨ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . compound 3 C31H50 ÏàËÆ¶È:63.3% Tetrahedron Letters 2004 45 3093-3096 Enzymatic cyclization of 26- and 27-methylidenesqualene to novel unnatural C31 polyprenoids by squalene:hopene cyclase Hideya Tanaka, Hiroshi Noguchi, Ikuro Abe Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 12-ursine-3,28-diol ÏàËÆ¶È:63.3% Natural Product Research and Development 2008 20 821-823 Studies on the Chemical Constituents of Ilex cornuta ZHANG Jie; YU Rong; WU Xia; YE Yun-hua; ZHOU Ya-wei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . ursolic acid ÏàËÆ¶È:63.3% Natural Product Research and Development 2006 18 942-944 Chemical Constituents of Hedyotis diffusa SI Jian-yong; CHEN Di-hua*; PAN Rui-le; ZHAO Xiao-hong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . betulinic acid ÏàËÆ¶È:63.3% Records of Natural Products 2013 7 65-68 Chemical Constituents, Antimicrobial and Cytotoxic Activities of Hypericum riparium (Guttiferae) Michel F. Tala1, Patricia D. Tchakam, Hippolyte K. Wabo, Ferdinand M. Talontsi, Pierre Tane, Jules R. Kuiate, L¨¦on A. apondjou and Hartmut Laatsch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . dysoxyhainic acid D C30H46O4 ÏàËÆ¶È:63.3% European Journal of Organic Chemistry 2009 2009 4818-4824 Ring A Modified Novel Triterpenoids from Dysoxylum hainanense Xiu-Feng He, Xiao-Ning Wang, Sheng Yin, Lei Dong and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . (25S)-5¦Á-Spirostan-25-ol C27H44O3 ÏàËÆ¶È:63.3% Organic Magnetic Resonance 1977 9 439-464 13C N.m.r. Spectra of steroids¡ªA Survey and Commentary J.W.Blunt and J.B.Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 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 |

2Â¥2013-12-06 20:08:36
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Mamatyuk Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . serrat-14-en-3¦Â,21¦Â,24,29-tetraol C30H50O4 ÏàËÆ¶È:66.6% Natural Product Research 2004 18 453-459 Serratane-type Triterpenoids from Huperzia Serrata Hui Zhou; Yun-Sen Li; Xiao-Tian Tong; Hui-Qing Liu; Shan-Hao Jiang; Da-Yuan Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . euscaphic acid ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2007 32 496-500 Studies on chemical constituents in fruits of Eucalyptus globulus YANG Xiuwei, GUO Qingmei Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3,21-diepiserratenediol C30H50O2 ÏàËÆ¶È:66.6% Phytochemistry 1994 37 209-211 Serratenes from the stem bark of Picea Jezoensis carr. hondoensis Reiko Tanaka, Rie Tsuboi, Shunyo Matsunaga Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 24-(E)-3-oxo-dammara-6-¦Â-hydroxy-20,24-dien-26-al C30H46O3 ÏàËÆ¶È:66.6% Tetrahedron 1997 53 6465-6472 First examples of dammarane triterpenes isolated from Celastraceae Haydee Ch¨¢vez, Ana Est¨¦vez-Braun, ¨¢ngel G. Ravelo, Antonio G. Gonz¨¢lez Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3¦Â-Butynyloxy-5,6-epoxycholestane ÏàËÆ¶È:64.5% Steroids 2007 72 729-735 6E-Hydroximinosteroid homodimerization by cross-metathesis processes Miriam Rega, Carlos Jim¨¦nez, Jaime Rodr¨ªguez Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 27-hydroxyambrein C30H54O3 ÏàËÆ¶È:63.3% Journal of Natural Products 2007 70 147-153 Chemical Transformation and Biological Activities of Ambrein, a Major Product of Ambergris from Physeter macrocephalus (Sperm Whale) Ya-Ching Shen,Shi-Yie Cheng,Yao-Haur Kuo,Tsong-Long Hwang,Michael Y. Chiang,and Ashraf Taha Khalil Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . yunganogenin C ÏàËÆ¶È:63.3% Chemical & Pharmaceutical Bulletin 1995 43 636-640 Five New Triterpene Glycosides from Wisteria branchybotrys (Leguminosae) Junei KINJO,Yoshie FUJISHIMA,Kazuyo SAINO,Rui-hua TIAN and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 11b ÏàËÆ¶È:63.3% Chemical & Pharmaceutical Bulletin 1988 36 1646-1663 Tannins and Related Compounds. LXVII. : Isolation and Characterization of Castanopsinins A-H, Novel Ellagitannins Containing a Triterpenoid Glycoside Core, from Castanopsis cuspidata var. sieboldii NAKAI. (3) MASAYUKI AGETA,GEN-ICHIRO NONAKA and ITSUO NISHIOKA Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Soyasapogenol B C30H50O3 ÏàËÆ¶È:63.3% Journal of Asian Natural Products Research 2005 7 237-243 Three new isoprenylated flavonoids from the roots of Sophora flavescens PEI-LAN DING, AI-JUN HOU and DAO-FENG CHEN Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (22S,23S,24R)-24-methyl-22,23-epoxy-3¦Á,5-cyclo-5¦Á-cholestan-6¦Â-yl acetate ÏàËÆ¶È:63.3% Journal of Natural Products 1985 Vol 48 756-765 Starfish Saponins, Part 22. Asterosaponins from the Starfish Halityle regularis: A Novel 22,23-Epoxysteroidal Gylcoside Sulfate Raffaele Riccio, Maria Iorizzi, Olinda Squillace Greco, Luigi Minale, Maurice Debray, Jean Luis Menou Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . daucosterol ÏàËÆ¶È:63.3% Natural Product Sciences 2009 15 181-184 Phytochemical Constituents from the Seeds of Lithospermum erythrorhizon Park, Jun-Yeon; Lee, Sul-Lim; Han, Saem; Kim, Hye-Min; Lee, Jeong-Min; Ahn, Young-Hee; Lee, Sook-Young; Lee, Sang-Hyun Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 21¦Â-Hydroxyserrat-14-en-3-one C30H48O2 ÏàËÆ¶È:63.3% Phytochemistry 1994 37 209-211 Serratenes from the stem bark of Picea Jezoensis carr. hondoensis Reiko Tanaka, Rie Tsuboi, Shunyo Matsunaga Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . olibanumol H C30H52O3 ÏàËÆ¶È:63.3% Chemical & Pharmaceutical Bulletin 2009 57 957-964 Absolute Stereostructures of Olibanumols A, B, C, H, I, and J from Olibanum, Gum-Resin of Boswellia carterii, and Inhibitors of Nitric Oxide Production in Lipopolysaccharide-Activated Mouse Peritoneal Macrophages Masayuki Yoshikawa, Toshio Morikawa, Hideo Oominami and Hisashi Matsuda Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . uvaol ÏàËÆ¶È:63.3% Chinese Traditional and Herbal Drugs 2002 33 888-889 ËÄ´¨Áúµ¨µÄÈýÝÆ³É·Ö Nam joon-young,ÁõÏòǰ,ÕųÐìÇ,³Êç¼§,Àî¼Ãîç,½²ýä¨ Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 3 C31H50 ÏàËÆ¶È:63.3% Tetrahedron Letters 2004 45 3093-3096 Enzymatic cyclization of 26- and 27-methylidenesqualene to novel unnatural C31 polyprenoids by squalene:hopene cyclase Hideya Tanaka, Hiroshi Noguchi, Ikuro Abe Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 12-ursine-3,28-diol ÏàËÆ¶È:63.3% Natural Product Research and Development 2008 20 821-823 Studies on the Chemical Constituents of Ilex cornuta ZHANG Jie; YU Rong; WU Xia; YE Yun-hua; ZHOU Ya-wei Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . ursolic acid ÏàËÆ¶È:63.3% Natural Product Research and Development 2006 18 942-944 Chemical Constituents of Hedyotis diffusa SI Jian-yong; CHEN Di-hua*; PAN Rui-le; ZHAO Xiao-hong Structure 13C NMR ̼Æ×Ä£Äâͼ |

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