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PSA: ½ð±Ò+1, ¸ÐлÄúµÄÈÈÐİïÖú 2012-12-04 11:29:29
hexiaoyang119: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£Ð»Ð»£¡ 2012-12-04 13:30:15
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PSA: ½ð±Ò+1, ¸ÐлÄúµÄÈÈÐİïÖú 2012-12-04 11:29:29
hexiaoyang119: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£Ð»Ð»£¡ 2012-12-04 13:30:15
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²éѯ½á¹û£º¹²²éµ½12¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . ´ó»Æ·Ó(chrysophanol) C15H10O4 ÏàËÆ¶È:73.3% Chinese Journal of Marine Drugs 2011 30(4) 18-24 Bioactive secondary metabolites produced by an Antarctic marine-derived fungus Penicil l ium chrysogenum PR4-1-3 MA Hong-yan,LI De-hai,GU Qian-qun,ZHU T ian-jiao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Chrysophanol ÏàËÆ¶È:73.3% Archives of Pharmacal Research 2008 31 598-605 Lipoxygenase inhibitory constituents from rhubarb Tran Minh Ngoc, Pham Thi Hong Minh, Tran Manh Hung, Phuong Thien Thuong and IkSoo Lee, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . chrysophanol ÏàËÆ¶È:73.3% Journal of China Pharmaceutical University 2003 34 216-219 Steroids and Anthraquinones from Astragalus hoantchy ZHAO Ming; DUAN Jin-Ao; HUANG Wen-Zhe; ZHOU Rong-Han; CHE Chun-Tao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . chrysophanol ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 2009 40 1359-1362 Chemical constituents from exocarp of Juglans mandshurica LIU Yuan-hui; CHENG Ze-feng; QIAO Wen-tao; YUAN Ke Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . Compound 2 ÏàËÆ¶È:56.2% Phytochemical Analysis 2002 13 114-120 New 3-deoxyanthocyanidins from leaves of Arrabidaea chica Beatriz Devia, Gabriel Llabres, Jan Wouters, Leon Dupont, Maria Teresa Escribano-Bailon, Sonia de Pascual-Teresa, Luc Angenot and Monique Tits Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 7-Hydroxy-2,8-dimethoxyonychine C15H13NO4 ÏàËÆ¶È:53.3% Phytochemistry 1995 38 1037-1048 Aporphinoid alkaloids and terpenoids from Piptostigma fugax Hans Achenbach, Andreas Schwinn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 8-chloro-3',4',5,7-tetrahydroxyisoflavone C15H9O6Cl ÏàËÆ¶È:53.3% The Journal of Antibiotics 1989 42 1350-1355 STRUCTURAL STUDY OF ISOFLAVONOIDS POSSESSING ANTIOXIDANT ACTIVITY ISOLATED FROM THE FERMENTATION BROTH OF STREPTOMYCES SP. SHINJI FUNAYAMA, YUMI ANRAKU, AKIRA MITA, KANKI KOMIYAMA, SATOSHI OMURA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 5-amino-4-oxo-3-(4-(trifluoromethoxy)phenyl)-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylic acid ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2012 20 4451-4461 Aminothienopyridazine inhibitors of tau aggregation: Evaluation of structure¨Cactivity relationship leads to selection of candidates with desirable in vivo properties Carlo Ballatore, Alex Crowe, Francesco Piscitelli, Michael James, Kevin Lou, Gabrielle Rossidivito, Yuemang Yao, John Q. Trojanowski, Virginia M.-Y. Lee, Kurt R. Brunden, Amos B. Smith III Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 10-epi-11-deoxy-¦Â-rhodomycinone C20H18O7 ÏàËÆ¶È:52.6% The Journal of Antibiotics 1995 48 1153-1158 New Anthracycline Antibiotics 10-epi-Oxaimomyciii and 10-epi-11-Deoxyoxaunomycin OSAMU JOHDO, H. NISHIDA, R. OKAMOTO, AKIHIRO YOSHIMOTO, TOMIO TAKEUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . dihydrocalythropsin C16H16O5 ÏàËÆ¶È:50% Journal of Natural Products 1993 Vol 56 1718 Two New Cytotoxic Chalcones from Calythropsis aurea John A. Beutler, John H. Cardellina II., Glenn N. Gray, Tanya R. Prather, Robert H. Shoemaker, Michael R. Boyd, Chii M. Lin, Ernest Hamel, Gordon M. Cragg Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . dehydroeffusal ÏàËÆ¶È:50% Phytochemistry 1991 30 3149-3151 Phenanthrene derivatives from the medullae of Juncus effusus Katsuhito Shima, Masao Toyota, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 3-[2-(5-bromo-2-oxoindolin-3-ylidene)hydrazinyl]qui-noxalin-2(1H)-one C16H10N5O2Br ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2010 18 214-221 Microwave assisted synthesis and antimicrobial activity of 2-quinoxalinone-3-hydrazone derivatives Olayinka O. Ajani, Craig A. Obafemi, Obinna C. Nwinyi, David A. Akinpelu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- |
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