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quluseobaby: ½ð±Ò+4, ¡ïÓаïÖú 2015-03-12 14:20:53
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quluseobaby: ½ð±Ò+4, ¡ïÓаïÖú 2015-03-12 14:20:53
quluseobaby(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+4 2015-05-03 10:22:53
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1 . alatoside F C21H30O8 ÏàËÆ¶È:61.9% Phytochemistry 2013 96 201-207 Eudesmane-type sesquiterpene derivatives from Laggera alata Guo-Cai Wang, Guo-Qiang Li, Hua-Wei Geng, Tao Li, Jiao-Jiao Xu, Fang Ma, Xia Wu, Wen-Cai Ye, Yao-Lan Li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . nicotabacoside B C20H32O7 ÏàËÆ¶È:60% Fitoterapia 2014 96 81-87 Noreudesmane sesquiterpenoids from the leaves of Nicotiana tabacum Cai-Yan Yang, Chang-An Geng, Xiao-Yan Huang, Hao Wang, Hong-Bo Xu, Wen-Juan Liang, Yun-Bao Ma, Xue-Mei Zhang, Jun Zhou, Ji-Jun Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . cucurbitoside F C24H36O12 ÏàËÆ¶È:59.0% Journal of Natural Products 2005 68 1754-1757 Cucurbitosides F−M, Acylated Phenolic Glycosides from the Seeds of Cucurbita pepo Wei Li, Kazuo Koike, Masaru Tatsuzaki, Atsushi Koide, and Tamotsu Nikaido Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3¦Â-[(¦Â-D-glucopyranosyl)oxy]eudesma- 4(14),11(13)-dien-12-ol C21H34O7 ÏàËÆ¶È:57.1% Helvetica Chimica Acta 2004 Vol. 87 1446 Eudesmane-Type Sesquiterpene Derivatives from Saussurea conica Cheng-Qi Fan, Zha-Jun Zhan, Hui Li, and Jian-Min Yue Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . alatoside D C21H32O8 ÏàËÆ¶È:57.1% Phytochemistry 2003 63 835-839 Eudesmane and megastigmane glucosides from Laggera alata Qunxiong Zheng, Zhaojun Xu, Xianfeng Sun, Wei Yao, Handong Sun,Christopher H. K. Cheng, Yu Zhao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . cucurbitoside K C23H34O12 ÏàËÆ¶È:57.1% Journal of Natural Products 2005 68 1754-1757 Cucurbitosides F−M, Acylated Phenolic Glycosides from the Seeds of Cucurbita pepo Wei Li, Kazuo Koike, Masaru Tatsuzaki, Atsushi Koide, and Tamotsu Nikaido Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . (1R,4R,5R,8R,9S)-4,5-Epoxycaryophyllane-14-ol 14-O-¦Â-D-glucopyranoside ÏàËÆ¶È:57.1% Phytochemistry 1994 35 635-639 Biotransformation of caryophyllene oxide by cultured cells of Eucalyptus perriniana Yutaka Orihara, Kenji Saiki, Tsutomu Furuya Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . Culcitiolide J C21H34O8 ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 2013 61 816-822 Culcitiolides E¨CJ, Six New Eremophilane-Type Sesquiterpene Derivatives from Senecio culcitioides Taichi Mitsui, Ken-ichiro Hayashi, Mikiko Kawai, Masahiro Kido, Hiroyuki Tani, Daisuke Takaoka, Nobuyasu Matsuura, Hiroshi Nozaki Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . swertiajaposide E C16H24O9 ÏàËÆ¶È:55% Helvetica Chimica Acta 2008 Vol. 91 1236 New Secoiridoid Glucosides from Swertia japonica Masafumi Kikuchi, Rie Kakuda, Yasunori Yaoita, and Masao Kikuchi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 8-epikingiside ÏàËÆ¶È:55% Helvetica Chimica Acta 2009 92 2063-2070 Three New Monoterpene Glucosides from Lamium amplexicaule Masao Kikuchi, Rie Onoguchi, Yasunori Yaoita Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 24-epi-teasterone-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:55% Phytochemistry 1998 48 467-470 Metabolic inversion of the 3-hydroxy function of brassinosteroids Adelheid Kolbe, Bernd Schneider, Andrea Porzel, G¨¹nter Adam Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 8-epikingiside ÏàËÆ¶È:55% Phytochemistry 1997 46 1035-1038 Secoiridoids from Gentiana siphonantha Ren Xiang Tan, Ling Dong Kong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 12a C20H34O5 ÏàËÆ¶È:55% Phytochemistry 1995 39 151-161 3-hydroxy-3-methylglutaryl dolabellane diterpenes from Chrozophora obliqua Khaled M. Mohamed, Kazuhiro Ohtani, Ryoji Kasai, Kazuo Yamasaki Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . Linarionoside B C19H34O7 ÏàËÆ¶È:55% Phytochemistry 1994 37 461-465 Linarionosides A¨CC and acyclic monoterpene diglucosides from Linaria japonica Hideaki Otsuka Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 13 C26H28O8 ÏàËÆ¶È:55% Phytochemistry 1988 27 469-472 Absolute structure of nepetaside,a new iridoid glucoside from Nepeta cataria Shan Xie,Shinichi Uesato,Hiroyuki Inouye,Tetsuro Fujita,Fujio Murai,Motoko Tagawa,Tetsuro Shingu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 8-epikingiside C17H24O11 ÏàËÆ¶È:55% Phytochemistry 1989 28 1409-1411 A secoiridoid glucoside from Ligustrum japonicum Hiroshi Kuwajima,Katsunori Matsuuchi,Kiyokazu Takaishi,Kenichiro Inoue,Tetsuro Fujita,Hiroyuki Inouye Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 8-epikingiside ÏàËÆ¶È:55% Phytochemistry 1989 28 2199-2201 8-epikingiside and its vanillate ester,isolated from Gentiana pyrenaica Julian Garcia,Stephane Lavaitte,Claude Gey Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . petiolin E C19H23ClO9 ÏàËÆ¶È:55% Heterocycles 2009 79 917-924 Petiolins D and E, Phloroglucinol Derivatives from Hypericum pseudopetiolatum var. kiusianum Naonobu Tanaka, Takaaki Kubota, Haruaki Ishiyama, Yoshiki Kashiwada, Yoshihisa Takaishi, Junji Ito, Yuzuru Mikami, Motoo Shiro, and Jun'ichi Kobayashi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . t-butyl [(2S,3aS,5R,6aR)-5-((S)1-(p-nitrobenzoyl-oxy)propyl)hexahydrofuro[2,3-b]furan-2-yl]acetate C22H29O8N ÏàËÆ¶È:55% Tetrahedron 2006 62 1102-1109 Stereochemical revision of communiols D and H through synthesis Masaru Enomoto, Takashi Nakahata, Shigefumi Kuwahara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . 8-epikingiside C17H24O11 ÏàËÆ¶È:55% Journal of the Chinese Chemical Society 1996 43 171-176 Secoiridoid Glycosides from Jasminum Polyanthum ÉòÑž´(Ya-Ching Shen);ÁÖÉÙÁê(Shao-Ling Lin);Öx«˜ÎÄ(Pei-Wen Hsieh);º†Ö¾ÖÒ(Chyh-Chung Chein) Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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