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danil1288
½ð³æ (ÕýʽдÊÖ)
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karl2100: ½ð±Ò+1, лл£¡ 2013-10-16 21:08:09
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karl2100: ½ð±Ò+1, лл£¡ 2013-10-16 21:08:09
ÌÆÙ»(¶¹¸ç´ú·¢): ½ð±Ò+10, лл 2013-10-22 08:41:50
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µÚÒ»¸ö ²éѯ½á¹û£º¹²²éµ½13¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . MT-4 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1999 47 1426-1432 Immunomodulatory Constituents from an Ascomycete, Microascus tardifaciens Haruhiro FUJIMOTO,Toshiyuki FUJIMAKI,Emi OKUYAMA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . MT-5 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1999 47 1426-1432 Immunomodulatory Constituents from an Ascomycete, Microascus tardifaciens Haruhiro FUJIMOTO,Toshiyuki FUJIMAKI,Emi OKUYAMA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . cladosporin ÏàËÆ¶È:61.9% Journal of Natural Products 1993 Vol 56 1397 Isocladosporin, a Biologically Active Isomer of Cladosporin from Cladosporium cladosporioides John M. Jacyno, John S. Harwood, Horace G. Cutler, Mee-Kyoung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . asperentin-6-O-methyl ether C17H22O5 ÏàËÆ¶È:57.1% Zeitschrift f¨¹r Naturforschung C 2012 67c 587-593 Plant Growth Activities of Aspyran, Asperentin,and its Analogues Produced by the Fungus Aspergillus sp. Yasuo Kimura, Naomi Shimomura, Fumiaki Tanigawa, Shozo Fujioka, and Atsumi Shimad Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (R)-4-phenyl-2-O-[¦Â-D-xylopyranosyl(1¡ú6)-¦Â-D-glucopyranosyl]butane C21H32O10 ÏàËÆ¶È:52.3% Journal of Asian Natural Products Research 2007 9 223-231 Total synthesis of natural product (R)-4-phenyl-2-O-[¦Â-Dxylopyranosyl(1 ¡ú 6)-¦Â-D-glucopyranosyl]butane and its epimer L.-J. HUANG, S.-J. HOU, J.-B. LI and D.-Q. YU Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . keto-form C13H13O4 ÏàËÆ¶È:52.3% Journal of Asian Natural Products Research 2005 7 627-632 Two new constituents from Rheum sublanceolatum LAN XIANG, XUE-HUI LIU, GUO-QIANG FAN, YU-XIN CUI, LI-JUN DU and JUN-HUA ZHENG Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 1-O-¦Á-L-arabinofuranosyl-(1¡ú6)-¦Â-D-glucopyranosyl-3,7-dimethyl-oct-2-en-7-ol C21H38O11 ÏàËÆ¶È:52.3% Chinese Traditional and Herbal Drugs 2005 36 1763-1767 Ingenane diterpene ester constituents from Tibetan medicine Euphorbia wallichii LI Yu-lin; SUO You-rui Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . asperentin-8-O-methyl ether C17H22O5 ÏàËÆ¶È:52.3% Zeitschrift f¨¹r Naturforschung C 2012 67c 587-593 Plant Growth Activities of Aspyran, Asperentin,and its Analogues Produced by the Fungus Aspergillus sp. Yasuo Kimura, Naomi Shimomura, Fumiaki Tanigawa, Shozo Fujioka, and Atsumi Shimad Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-10-16 18:19:34
danil1288
½ð³æ (ÕýʽдÊÖ)
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µÚ¶þ¸ö ²éѯ½á¹û£º¹²²éµ½114¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Penijanthine A C27H33NO3 ÏàËÆ¶È:67.8% Journal of Natural Medicines 2009 63 96-99 A new indoloditerpene derivative, penijanthine A, isolated from Penicillium janthinellum Takeshi Itabashi, Tomoo Hosoe, Daigo Wakana, Kazutaka Fukushima and Kayoko Takizawa, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . paxilline ÏàËÆ¶È:64.2% Chemical & Pharmaceutical Bulletin 1990 38 3473-3475 Structures of New Indoloditerpenes, Possible Biosynthetic Precursors of the Tremorgenic Mycotoxins, Penitrems, from Penicillium crustosum Tomoo HOSOE,Koohei NOZAWA,Shun-ichi UDAGAWA,Shoichi NAKAJIMA and Ken-ichi KAWAI Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . paxilline ÏàËÆ¶È:64.2% Chemical & Pharmaceutical Bulletin 1989 37 1387-1389 Isolation of a New Tremorgenic Indologiterpene, 1'-O-Acetylpaxilline, from Emericella striata and Distribution of Paxilline in Emericella spp. Koohei NOZAWA,Yoshikazu HORIE,Shun-ichi UDAGAWA,Ken-ichi KAWAI and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . hispidone C28H36O5 ÏàËÆ¶È:64.2% Phytochemistry 1992 31 1335-1338 Limonoids and protolimonoids from the fruits of Phellodendron amurense Kuki Kishi, Kazuko Yoshikawa, Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Paxilline ÏàËÆ¶È:64.2% Journal of Natural Medicines 2009 63 96-99 A new indoloditerpene derivative, penijanthine A, isolated from Penicillium janthinellum Takeshi Itabashi, Tomoo Hosoe, Daigo Wakana, Kazutaka Fukushima and Kayoko Takizawa, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . proceranone C28H36O5 ÏàËÆ¶È:64.2% Phytochemistry 1981 20 173-174 Proceranone, a new tetranortriterpenoid from Carapa procera B. L. Sondengam, C. S. Kamga, S. F. Kimbu, J. D. Connolly Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 5 ÏàËÆ¶È:64.2% Journal of the Chemical Society, Perkin Transactions 1 1981 1750-1753 Tetranortriterpenoids and related compounds. Part 26. Tecleanin, a possible precursor of limonin, and other new tetranortriterpenoids from Teclea grandifolia Engl. (Rutaceae) J. Foyere Ayafor, B. Lucas Sondengam, Joseph D. Connolly, David S. Rycroft and Joseph I. Okogun Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . paxilline ÏàËÆ¶È:64.2% Journal of the Chemical Society, Perkin Transactions 1 1988 2607-2610 Isolation and structures of indoloditerpenes, possible biosynthetic intermediates to the tremorgenic mycotoxin, paxilline, from Emericella striata Koohei Nozawa, Shoichi Nakajima, Ken-ichi Kawai and Shun-ichi Udagawa Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2013-10-16 18:24:36














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