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À¶Ý®Ììʹ2012(¶¹¸ç´ú·¢): ½ð±Ò+5, лл 2013-11-14 15:31:22
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À¶Ý®Ììʹ2012(¶¹¸ç´ú·¢): ½ð±Ò+5, лл 2013-11-14 15:31:22
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Ï´ÎÇë °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 È磺21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ²éѯ½á¹û£º¹²²éµ½932¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . (22E,24R)-3¦Â,5¦Á,9¦Á-trihydroxyergosta-7,22-dien-6-one ÏàËÆ¶È:75% Chinese Journal of Marine Drugs 2009 28(5) 11-16 Cytotoxic metabolites from symbiotic fungus Penicilliom sp.HK13-8 with Rhizophora stylosa HAN Xiu-li, LIN Zhen-jian, TAO Hong-wen, LIU Pei-pei, WANG Yi, ZHU Wei-ming Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 3¦Â,5¦Á,9¦Á-trihydroxyl-(22E,24R)-ergosta-7,22-diene-6-one ÏàËÆ¶È:75% Natural Product Research and Development 2012 24 1047-1050 Secondary Metabolites from Marine Fungus Fusarium sp. LIU Tao; LI Zhan-lin; WANG Yu; TIAN Li; PEI Yue-hu; HUA Hui-ming Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 3¦Â,5¦Á,9¦Á-trihydroxy-(22E,24R)-ergosta-7,22-dien-6-one C28H44O4 ÏàËÆ¶È:71.4% Chemistry of Natural Compounds 2009 45 759-761 STEROIDS AND OTHER CONSTITUENTS FROMTHE MUSHROOM Armillaria lueo-virens Hui-Yan Xiong, Dong-Qing Fei, Jin-Song Zhou,Chun-Jiang Yang,and Guo-Liang Ma Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,9¦Á-trihydroxy-6-one C28H44O4 ÏàËÆ¶È:71.4% Natural Product Research and Development 2007 19 436-438 Chemical Constituents of Basidiomycetes Russula subnigricans GONG Qing-fang; ZHANG Yu-mei; TAN Ning-hua; CHEN Zuo-hong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 3¦Â,5¦Á,9¦Á-ÈýôÇ»ù-(22E,24R)-Âó½ÇçÞ-7,22-¶þÏ©-6-ͪ ÏàËÆ¶È:71.4% Journal of Chinese Medicinal Materials 2007 30 655-657 Studies on Chemical Constituents of Marine Bryozoan Bugula neritina L. TANG Hua, CHENG Ping, LIN Hou-wen, GAO Wen, LU Yi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 3¦Â,5¦Á,9¦Á-trihydroxy-(22E,24R)-ergosta-7,22-dien-6-one ÏàËÆ¶È:71.4% Journal of Chinese Medicinal Materials 2011 34 180-183 Sterols of Marine Bryozoan Bugula neritina from the South China Sea LEI Hui, ZHOU Xue-feng, YANG Ya-ling, SUN Jian-fan, HU Jing, LIU Yong-hong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . dehydro ergosterol peroxide ÏàËÆ¶È:70.8% Archives of Pharmacal Research 1994 17 1-4 Some sesquiterpenoids and 5¦Á,8¦Á-epidioxysterols from Solanum lyratum Su Mi Yu, Hyoung Ja Kim, Eun-Rhan Woo and Hokoon Park Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 3¦Â,5¦Á,9¦Á-trihydroxyergosta-7,22-dien-6-one ÏàËÆ¶È:67.8% Natural Product Research and Development 2012 24 1747-1749 Chemical Constituents of Favolus arcularius YIN Wei, LIU Jin-song, WU Pei-yun, LIANG Yi-min, WANG Gang* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 24E-ergosta-7,22-dien-6-one-3¦Â,5¦Á-diol C28H44O3 ÏàËÆ¶È:66.6% Natural Product Research and Development 1992 4(2) 44-47 CHEMICAL RESEARCH ON THE METABOLITES OF LACTARIUS HYSGINUS (¢ñ) Dong Ding* Wang Huaibin Li Guangyi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 9,11-Dehydroergosterol peroxide ÏàËÆ¶È:65.3% Korean Journal of Pharmacognosy 2007 38(2) 164-169 Antioxidative Activities of Phenolic Compounds Isolated from Inonotus obliquus Kim, Hyoung-Ja; Jin, Chang-Bae; Lee, Yong-Sup Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (22E,24R)-ergosta-6,9,22-trien-3¦Â,5¦Á,8¦Á-triol ÏàËÆ¶È:64.2% Natural Products and Bioprospecting 2012 2 240-244 Six novel steroids from culture of basidiomycete Polyporus ellisii Shuang Wang, Ling Zhang, Liang-Yan Liu, Ze-Jun Dong, Zheng-Hui Li, Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 3 ¦Â,5¦Á-dihydroxy-(22E,24R)-ergosta-7,22-dien-6-one C28H44O3 ÏàËÆ¶È:64.2% Natural Product Research 2013 27 1611-1619 Bioactive ergostanoids and a new polyhydroxyoctane from Lentinus polychrous mycelia and their inhibitory effects on E2-enhanced cell proliferation of T47D cells Niramai Fangkrathok, Bungorn Sripanidkulchai, Kaoru Umehara & Hiroshi Noguchi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 13-epi-homoverrucosan-5¦Â,6¦Â-diol C20H34O2 ÏàËÆ¶È:60.8% Phytochemistry 1995 40 199-203 13-Epi-homoverrucosane derivatives and other diterpenes from Plagiochila (hepaticae) Susanne Valcic, Volker Huch, Michael Veith, Hans Becker Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . ent-3¦Â-hydroxy-beyer-15-ene-2-one C20H30O2 ÏàËÆ¶È:60.8% Phytochemistry 1992 31 699-702 Diterpenoids from Spirostachys africana Zvitendo James Duri, Neil Arthur Hughes, Namboole Moses Munkombwe Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . ent-3¦Â,18-isopropylidenedioxy-beyer-15-ene-2-one C23H34O3 ÏàËÆ¶È:60.8% Phytochemistry 1992 31 699-702 Diterpenoids from Spirostachys africana Zvitendo James Duri, Neil Arthur Hughes, Namboole Moses Munkombwe Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . senepodine A ÏàËÆ¶È:60.8% Heterocycles 2009 77 679-729 The Lycopodium Alkaloids Yusuke Hirasawa, Jun'ichi Kobayashi, and Hiroshi Morita Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 3¦Â-Hydroxy-14-oxo-14,15-seco-5¦Â-card-20( 22)-enolide-15-nitrile C23H31NO4 ÏàËÆ¶È:60.8% Steroids 1996 61 572-582 Digitalis-like compounds: Synthesis and biological evaluation of seco-D and D-homo derivatives Mauro Gobbini, Alessandra Benicchio, Giuseppe Marazzi, Gloria Padoani, Marco Torri, Piero Melloni Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . (1R,3aR,5R,7aR,1'R,2'E,4'R)-5,6,7,7a-Tetrahydro-5-bromoacetoxy-7a-methyl-1-(1',4',5'-trimethyl-2'-hexenyl)-3aH-indan-4-one C21H33O3Br ÏàËÆ¶È:60.8% Tetrahedron 2012 68 1729-1735 Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine A Arata Yajima, Yuuma Kagohara, Keisuke Shikai, Ryo Katsuta, Tomoo Nukada Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (3aR,3bR,5aR,6R,8aR,1'R,2'E,4'R)-3a,3b,4,5,5a,7,8,8a-Octahydro-3a-hydroxy-5a-methyl-6-(1',4',5'-trimethyl-2'-hexenyl)-2H-indeno[5,4-b]dihydrofuran-2-one C21H34O3 ÏàËÆ¶È:60.8% Tetrahedron 2012 68 1729-1735 Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine A Arata Yajima, Yuuma Kagohara, Keisuke Shikai, Ryo Katsuta, Tomoo Nukada Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . (3bR,5aR,6R,8aR,1'R,20E,4'R)-3a,3b,4,5,5a,7,8,8a-Octahydro-5a-methyl-6-(1',4',5'-trimethyl-2'-hexenyl)-2H-indeno[5,4-b]furan-2-one C21H32O2 ÏàËÆ¶È:60.8% Tetrahedron 2012 68 1729-1735 Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine A Arata Yajima, Yuuma Kagohara, Keisuke Shikai, Ryo Katsuta, Tomoo Nukada Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . volemolide C22H34O3 ÏàËÆ¶È:60.8% Bioscience, Biotechnology, and Biochemistry 1994 58 1542-1544 Volemolide, a Novel Norsterol from the Fungus Lactarius volemus Kenji Kobata, Tomonari Wada, Yasuo Hayashi, Hisao Shisata Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . volemolide C22H36O3 ÏàËÆ¶È:60.8% Natural Product Research and Development 2010 22 786-788 Chemical Constituents of Culture Broth of Hebeloma westraliense SHAO Hong-jun;FANG Li-zhen; LIU Ji-kai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . Voulkens in E C20H32O2 ÏàËÆ¶È:60.8% Bioorganic & Medicinal Chemistry Letters 2013 23 3088-3095 Voulkensin C¨CE, new 11-oxocassane-type diterpenoids and a steroid glycoside from Caesalpinia volkensii stem bark and their antiplasmodial activities Charles O. Ochieng, Lawrence A.O. Manguro, Philip O. Owuor, Hosea Akala Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . (22E)-5a,8a-epidioxyergosta-6,9(11),22-trien-3b-ol ÏàËÆ¶È:60.7% Chemistry & Biodiversity 2008 Vol. 5 743 Chemical Constituents of Stereum subtomentosum and Two Other Birch-Associated Basidiomycetes: An Interspecies Comparative Study Simona Hybelbauerov¨¢, Jan Sejbal, Martin Drač¨ªnský , Alice Hahnov¨¢, and Bohum¨ªr Koutek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 9(11)-dehydroaxinysterol C28H40O3 ÏàËÆ¶È:60.7% Chemical & Pharmaceutical Bulletin 2002 50(9) 1286-1289 New Biologically Active Marine Sesquiterpenoid and Steroid from the Okinawan Sponge of the Genus Axinyssa Makoto IWASHIMA,Ikuo TERADA,Kazuo IGUCHI,and Takao YAMORI Structure 13C NMR ̼Æ×Ä£Äâͼ |
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