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²éѯ½á¹û£º¹²²éµ½363¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 4, 4'-dimethoxy-3'-hydroxy-7, 9'¡Ã7', 9-diepoxylignan-3-O-¦Â-D-glucopyranoside C26H32O11 ÏàËÆ¶È:92.5% Acta Botanica Yunnanica 2003 25(6) 711-715 A New Lignan Glycoside from Curculigo capitulata LI Ning,TAN Ning-Hua,ZHOU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . pinoresinol-4-O-¦Â-D-glucopyranoside ÏàËÆ¶È:92.5% Chinese Traditional and Herbal Drugs 2008 39 654-656 Chemical constituents of Selaginella sinensis FENG Wei-sheng; CHEN Hui; ZHENG Xiao-ke Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (+)-pinoresinol-O-¦Â-D-glucopyranoside ÏàËÆ¶È:92.5% Chinese Traditional and Herbal Drugs 2008 39 343-346 ÏãÁÛëާÖÐÄ¾Ö¬ËØÀ࿹Ñõ»¯»îÐԳɷֵÄÑо¿ ÕÅÑåÁú;ÔøÎ°Ãñ;Íõ»ÛÈÙ;ÖìÀö;ÐìºéÁÁ;¿ïº£Ñ§ Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Pinoresinol-4-O-glucoside ÏàËÆ¶È:92.5% Archives of Pharmacal Research 2005 28 39-43 Antitumor and antiinflammatory constituents from celtis sinensis Dae Keun Kim, Jong Pil Lim, Jin Wook Kim, Hee Wook Park and Jae Soon Eun Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (+)-pinoresinol-4'-O-¦Â-D-glucopyranoside ÏàËÆ¶È:92.5% Acta Pharmaceutica Sinica 2013 48 521-525 Chemical constituents from Pachysandra terminalis XIAO Hui-jun, LI Chen-yang, TANG Sheng-an, QIN Nan, DUAN Hong-quan Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (-)-pinoresinol 4-O-¦Â-D-glucopyranosid ÏàËÆ¶È:92.5% Journal of Tropical and Subtropical Botany 2012 20 206-208 Five Glycosides from the Seeds of Litchi chinensis XU Xin-ya, XIE Hai-hui, WEI Xiao-yi Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (+)-Pinoresinol-O-¦Â-D-glucopyranoside C26H32O11 ÏàËÆ¶È:88.8% Acta Botanica Yunnanica 2006 28(4) 429-432 Non2alkaloid Constituents of Buxus sinica (Buxaceae) LIN Yun-Liang, QIU Ming-Hua, LI Zhong-Rong,ZHOU Lin,LIU Jian-Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (+)-pinoresinol O-¦Â-D-glucopyranoside ÏàËÆ¶È:88.8% Phytochemistry 2009 70 1277-1285 Absolute configuration of (+)-pinoresinol 4-O-[6''-O-galloyl]-¦Â-D-glucopyranoside,macarangiosides E, and F isolated from the leaves of Macaranga tanarius Katsuyoshi Matsunami, Hideaki Otsuka, Kazunari Kondo, Takakazu Shinzato, Masatoshi Kawahata, Kentaro Yamaguchi, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (-)-pinoresinol 4-O-¦Â-D-glucopyranoside ÏàËÆ¶È:88.8% China Journal of Chinese Materia Medica 2006 31 133-135 Chemical constituents from root of Lasianthus acuminatissimus I LI Bin, ZHANG Dongming, LUO Yongming Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Pinoresinol-4-O-¦Â-D-glucopyranoside C26H32O11 ÏàËÆ¶È:88.8% Natural Product Research and Development 2012 24 298-302 Vasorelaxant Effect on Isolated Rabbit Aortic Rings and Chemical Constituents of n-Butanol Fraction from Leaves of Magnolia officinalis Rehd et Wils. YANG Zhu-ya; WEI Ying-fang; ZHOU Zhi-hong; LONG Fei Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (-)-Pinoresinol 4-O-¦Â-D-glucopyranoside ÏàËÆ¶È:85.1% Phytochemistry 1994 35 479-483 Lignans and a stilbene from Festuca argentina Adriana C. Casabuono, Alicia B. Pomillo Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 4,4'-dimethoxy-3'-hydroxy-7,9',7',9-diepoxyligan-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:85.1% Natural Product Research and Development 2010 22 731-735 Studies on the Chemical Constituents of Euphorbia helioscopia HE Jiang-bo;LIU Guang-ming; CHENG Yong-xian Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (+)-pinoresinol 4-O-glucoside ÏàËÆ¶È:85.1% Natural Medicines 1995 49 475-477 Studies on the Constituents of Chinese Medicine "Luobumaye" : On Phenolic Compounds of Poacynum hendersonii Leaves LEI ZHEN-HUAN,YAHARA SHOJI, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ËÉÖ¬ËØ-4-O-¦Â-D-ÆÏÌÑÌÇÜÕ ÏàËÆ¶È:85.1% Journal of Chinese Medicinal Materials 2007 30 792-794 Non-saponins from Solanum nigrum L. WANG Li-ye, WANG Nai-li, YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3'-demethyl-phillyrin C26H32O11 ÏàËÆ¶È:81.4% Natural Product Research and Development 2008 20 278-279 Chemical constituents from Tinospora sinensis REN Yan-li;TANG Qian-rui; ZHANG Zhen; CHEN Li; HE Hong-ping; HAO Xiao-jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ËÉÓÍ´¼-4-O-¦Â-D-ÇÛ²ËÌÇ»ù-(1¡ú2)-¦Â-D-ßÁà«ÆÏÌÑÌÇß° ÏàËÆ¶È:78.5% Journal of Tropical and Subtropical Botany 2005 13 171-174 °åÀ¶¸ùÖÐß°Àà³É·ÖµÄÑо¿ κ»¶»¶, ÎâÆ¼, κТÒå, ¼ªÌïÑÅÖ®, лº£»Ô Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . pinoresinol 4-O-¦Á-L-rhamnopyranosyl (1¡ú 2)-¦Â-D-gluco-pyranoside C32H42O15 ÏàËÆ¶È:78.1% Journal of Natural Medicines 2009 63 100-101 Lignan and flavonoid glycosides from Urtica laetevirens Maxim. Yuan Zhou, Wei Wang, Ling Tang, Xing-guo Yan and Li-ying Shi, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . lanicepside B ÏàËÆ¶È:77.7% Helvetica Chimica Acta 2007 Vol. 90 951 Two New Lignan Glycosides from Saussurea laniceps Zhi-Wang Zhou, Sheng Yin, Xiao-NingWang, Cheng-Qi Fan, Hui Li, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (+)-isoeucommin A ÏàËÆ¶È:77.7% Natural Product Communications 2011 6 1901-1904 Two New Phenolic Glycosides from Viburnum plicatum var. plicatum f. plicatum Saki Katagiri, Yoshiki Watanabe, Yasunori Yaoita, Masao Kikuchi and Koichi Machida Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (+)-epipinoresinolmethyl ether-¦Â-D-glucoside C21H24O6 ÏàËÆ¶È:77.7% Pharmaceutical Biology 2002 40 96-102 The First Report on the Occurrence of Furofuranoid Lignan Glucosides in Acanthaceae El-Domiaty M.M., El-Shafae A.M., Abdel-Aal M.M., Abou-Hashem M.M. Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . (-)-(7R,7'R,8S,8'R)-4,4'-Dihydroxy-3,3'-dimethoxy-7,7'-epoxylignan-4-O-¦Â-D-glucopyranoside C26H34O10 ÏàËÆ¶È:77.7% Journal of Asian Natural Products Research 2013 15 482-491 Glycosides from the bark of Machilus robusta Peng-Bin Bu, Yan-Ru Li, Ming Jiang, Fang Wang, Xiao-Liang Wang, Sheng Lin, Cheng-Gen Zhu & Jian-Gong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (-)-(7R,7'R,8S,8'R)-4,4'-Dihydroxy-3,3'-dimethoxy-7,7'-epoxylignan-4'-O-¦Â-D-glucopyranoside C26H34O10 ÏàËÆ¶È:77.7% Journal of Asian Natural Products Research 2013 15 482-491 Glycosides from the bark of Machilus robusta Peng-Bin Bu, Yan-Ru Li, Ming Jiang, Fang Wang, Xiao-Liang Wang, Sheng Lin, Cheng-Gen Zhu & Jian-Gong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . (+)-Pinoresinol 4-O-[6''-O-galloyl]-¦Â-D-glucopyranoside C33H36O15 ÏàËÆ¶È:74.1% Phytochemistry 2009 70 1277-1285 Absolute configuration of (+)-pinoresinol 4-O-[6''-O-galloyl]-¦Â-D-glucopyranoside,macarangiosides E, and F isolated from the leaves of Macaranga tanarius Katsuyoshi Matsunami, Hideaki Otsuka, Kazunari Kondo, Takakazu Shinzato, Masatoshi Kawahata, Kentaro Yamaguchi, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . neoarctin A C26H34O12 ÏàËÆ¶È:74.0% Journal of Asian Natural Products Research 2007 9 541-544 A new lignan from the seeds of Arctium lappa MIN YONG, GU KUN and MIN-HUA QIU Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 7R,7' R,8S,8'S-( +)-neo-olivil 4-O-¦Â-D-Glucopyranoside C26H34O12N ÏàËÆ¶È:74.0% Chemical & Pharmaceutical Bulletin 2005 53 48-51 Studies on the Constituents of Swertia japonica MAKINO II. On the Structures of New Glycosides Masafumi Kikuchi and Masao Kikuchi Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . erythro-1-(4-O-¦Â-glucopyranosyl-3-methoxyphenyl)-2-{2-methoxyl-4-[1-(E)-propene-3-ol]-phenoxyl}-propane-1,3-diol C27H34O13 ÏàËÆ¶È:74.0% Turkish Journal of Chemistry 2005 29 71-81 Secondary Metabolites of Phlomis viscosa and Their Biological Activities İHSAN ÇALIŞ, HASAN KIRMIZIBEKMEZ, JOHN A. BEUTLER, ALİ ARSLAN DÖNMEZ, FUNDA NURAY YALÇIN, EKREM KILIÇ, MERAL ÖZALP, PETER R¨¹EDI, DENİZ TAŞDEMİR Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . Hyuganoside IIIa C26H34O12 ÏàËÆ¶È:74.0% Natural Product Research and Development 2012 24 1007-1013 Chemical Constituents from the Stems of Dipteronia dyeriana Henry GUO Rong; WANG Yue-hu; SHI Ya-na; LI Xing-yu; LI Wen-chang; LONG Chun-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . Hyuganoside IIIb C26H34O12 ÏàËÆ¶È:74.0% Natural Product Research and Development 2012 24 1007-1013 Chemical Constituents from the Stems of Dipteronia dyeriana Henry GUO Rong; WANG Yue-hu; SHI Ya-na; LI Xing-yu; LI Wen-chang; LONG Chun-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . Pinoresinol-4-O-rutinoside ÏàËÆ¶È:71.8% Archives of Pharmacal Research 2005 28 39-43 Antitumor and antiinflammatory constituents from celtis sinensis Dae Keun Kim, Jong Pil Lim, Jin Wook Kim, Hee Wook Park and Jae Soon Eun Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . lanicepside A C26H34O12 ÏàËÆ¶È:70.3% Helvetica Chimica Acta 2007 Vol. 90 951 Two New Lignan Glycosides from Saussurea laniceps Zhi-Wang Zhou, Sheng Yin, Xiao-NingWang, Cheng-Qi Fan, Hui Li, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ |
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