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1 . (3b)-3-(acetyloxy)lanosta-7,9(11),24-trien-21-oic acid C32H48O4 ÏàËÆ¶È:78.1% Helvetica Chimica Acta 2013 96 2092-2097 Lanostane Triterpenes from Ceriporia lacerate HS-ZJUT-C13A, a Fungal Endophyte of Huperzia serrata You-Min Ying, Wei-Guang Shan, Li-Wen Zhang, Yan Chen and Zha-Jun Zhan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 8b ÏàËÆ¶È:78.1% Magnetic Resonance in Chemistry 1989 27 1012-1024 1H and 13C NMR assignments for lanostan-3¦Â-ol derivatives: Revised assignments for lanosterol Gary T. Emmons, William K. Wilson and George J. Schroepfer Jr Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¦Â-acetyl-16¦Á-hydroxydehydrotra-metenolic acid phthalimidomethyl ester C41H53O7N ÏàËÆ¶È:75.7% Phytochemistry 1995 40 225-231 Isolation of lanostane-type triterpene acids having an acetoxyl group from sclerotia of Poria cocos Takaaki Tai, Tetsuro Shingu, Tohru Kikuchi, Yasuhiro Tezuka, Akira Akahori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . lanosta-7,9(11),24-trien-3¦Â,21-diol ÏàËÆ¶È:75% Phytochemistry 1999 52 1621-1627 Steroids from the fungus Fomitopsis pinicola Joachim Rosecke, Wilfried A. Konig Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 3¦Á,16¦Á-dihydroxylanosta-7,9(11),24-trien-21-oic acid C30H46O4 ÏàËÆ¶È:71.8% Journal of Natural Products 2006 69 1245-1248 Lanostane Triterpenoids from the Sri Lankan Basidiomycete Ganoderma applanatum E. Dilip de Silva, Sonia A. van der Sar, R. G. Lalith Santha, Ravi L. C.Wijesundera, Anthony L. J. Cole, John W. Blunt, and Murray H. G. Munro Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 21-hydroxylanosta-7,9(11),24-trien-3-one ÏàËÆ¶È:71.8% Phytochemistry 1999 52 1621-1627 Steroids from the fungus Fomitopsis pinicola Joachim Rosecke, Wilfried A. Konig Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . Hypocrellol B C32H50O4 ÏàËÆ¶È:71.8% Journal of Natural Products 2011 74 2143−2150 Lanostane and Hopane Triterpenes from the Entomopathogenic Fungus Hypocrella sp. BCC 14524 Masahiko Isaka, Panida Chinthanom, Malipan Sappan, Rungtiwa Chanthaket,J. Jennifer Luangsa-ard, Samran Prabpai, and Palangpon Kongsaeree Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 3¦Á,16¦Á-Dihydroxylanosta-7,9(11),24-trien-21-oic acid ÏàËÆ¶È:71.8% Molecules 2014 19 17478-17535 A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp. Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . inonotsulide C C30H46O3 ÏàËÆ¶È:68.7% Helvetica Chimica Acta 2007 Vol. 90 2047 Three New Lanostane Triterpenoids from Inonotus obliquus Sayaka Taji, Takeshi Yamada, Yasuko In, Shun-ichi Wada, Yoshihide Usami, Kazuo Sakuma, and Reiko Tanaka Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 3¦Á,16¦Á,26-trihydroxylanosta-7,9(11),24-trien-21-oic acid C30H46O5 ÏàËÆ¶È:68.7% Journal of Natural Products 2006 69 1245-1248 Lanostane Triterpenoids from the Sri Lankan Basidiomycete Ganoderma applanatum E. Dilip de Silva, Sonia A. van der Sar, R. G. Lalith Santha, Ravi L. C.Wijesundera, Anthony L. J. Cole, John W. Blunt, and Murray H. G. Munro Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . antiquol C acetate C32H50O2 ÏàËÆ¶È:68.7% Journal of Natural Products 2002 65 158-162 Eupha-7,9(11),24-trien-3â-ol (¡°Antiquol C¡±) and Other Triterpenes from Euphorbia antiquorum Latex and Their Inhibitory Effects on Epstein-Barr Virus Activation Toshihiro Akihisa, E. M. Kithsiri Wijeratne, Harukuni Tokuda, Fumio Enjo, Masakazu Toriumi,Yumiko Kimura, Kazuo Koike, Tamotsu Nikaido, Yasuhiro Tezuka, and Hoyoku Nishino Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 3¦Â,16¦Á-dihydroxylanosta-7,9(11),24-trien-21-oic acid ÏàËÆ¶È:68.7% Chemical & Pharmaceutical Bulletin 1996 44 847-849 Isolation of Inhibitors of TPA-Induced Mouse Ear Edema from Hoelen, Poria cocos Haruo NUKAYA,Hirokazu YAMASHIRO,Hirotatsu FUKAZAWA,Hitoshi ISHIDA and Kuniro TSUJI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . ganodercochlearin C C31H50O3 ÏàËÆ¶È:68.7% Journal of Natural Products 2014 77 737-743 Hepatoprotective Effects of Triterpenoids from Ganoderma cochlear Xing-Rong Peng, Jie-Qing Liu, Cui-Fang Wang, Xu-Yang Li, Yi Shu, Lin Zhou, and Ming-Hua Qiu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . compound II ÏàËÆ¶È:68.7% Journal of Agricultural and Food Chemistry 1990 38 134-137 Isolation and characterization of pentacyclic triterpene ovipositional stimulant for the sweet potato weevil from Ipomoea batatas (L.) Lam Ki Cheol Son, Ray F. Severson, Richard F. Arrendale, Stanley J. Kays Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . boehmerol ÏàËÆ¶È:68.7% Journal of Agricultural and Food Chemistry 1990 38 134-137 Isolation and characterization of pentacyclic triterpene ovipositional stimulant for the sweet potato weevil from Ipomoea batatas (L.) Lam Ki Cheol Son, Ray F. Severson, Richard F. Arrendale, Stanley J. Kays Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . agnosterol ÏàËÆ¶È:68.7% Magnetic Resonance in Chemistry 1989 27 1012-1024 1H and 13C NMR assignments for lanostan-3¦Â-ol derivatives: Revised assignments for lanosterol Gary T. Emmons, William K. Wilson and George J. Schroepfer Jr Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 9b ÏàËÆ¶È:68.7% Magnetic Resonance in Chemistry 1989 27 1012-1024 1H and 13C NMR assignments for lanostan-3¦Â-ol derivatives: Revised assignments for lanosterol Gary T. Emmons, William K. Wilson and George J. Schroepfer Jr Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 3¦Á-acetoxylanosta-8,24-dien-21-oic acid ÏàËÆ¶È:68.7% Drugs & Clinic 2013 28 822-825 Chemical constituents in ethyl acetate fraction from Olibanum ZHAO Na-xia, CHANG Yun-ping, XIA Guang-ping, ZHANG Jun-yan, HAN Ying-mei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . 3¦Á,16¦Á,26-Trihydroxylanosta-7,9(11),24-trien-21-oic acid ÏàËÆ¶È:68.7% Molecules 2014 19 17478-17535 A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp. Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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