| ²é¿´: 186 | »Ø¸´: 1 | ||
[ÇóÖú]
΢Æ×ÇóÖú£¬ÐÁ¿à
|
| 29.3,111.5,120.6,120.9,122.2,126.2,132.0,136.8 |
» ²ÂÄãϲ»¶
284Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
266Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
±¾¿ÆÉúÎïÐÅϢѧ£¬×Ü·Ö362 Çó07 08µ÷¼Á
ÒѾÓÐ3È˻ظ´
283Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
333Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
286Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ7È˻ظ´
297Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
312Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
085602»¯Ñ§¹¤³Ì268·Ö¶×µ÷¼Á
ÒѾÓÐ9È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×Êý¾ÝÇóÖú¡ª¡ªÈý¸ö»¯ºÏÎï лл£¡
ÒѾÓÐ8È˻ظ´
JYN-33 ΢Æ×ÇóÖú£¬¼±Çó£¬Ð»Ð»£¬×·¼Ó½ð±Ò¡£¡£¡£
ÒѾÓÐ6È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú(±½»·ÑÜÉúÎïÀà)
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾ÝÇóÖú ¼±±ÏÒµ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ñ·Ò»: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл£¡ 2013-11-02 13:47:35
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ñ·Ò»: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл£¡ 2013-11-02 13:47:35
|
²éѯ½á¹û£º¹²²éµ½440¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 1H-ßÅßá-2-ôÈËá ÏàËÆ¶È:87.5% Modern Chinese Medicine 2008 10(12) 29-31 Studies on the Metabolites of Salvianolic Acid B Yuan Zheng, Li Guoyu, , Zeng Yimei, Wang Jinhui Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 1H-indole-3-carboxylicacid ÏàËÆ¶È:77.7% China Journal of Chinese Materia Medica 2009 34 994-998 Chemical constituents of A lisma orientalis and their immunosuppressive function ZHANG Chaofeng, ZHOU Aichun, ZHANG mian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . bis(3-indolyl) ketone C17H12N2O ÏàËÆ¶È:77.7% Heterocycles 2004 63 2371-2377 Effect of Sodium Naphthalenide, a Key Set Reagent, on 3-Substituted Indoles Avijit Banerji*, Debasish Bandyopadhyay, and Bidyut Basak Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . indolyl-3-carboxylic acid C9H7NO2 ÏàËÆ¶È:77.7% Chinese Traditional and Herbal Drugs 2010 41 870-873 Áõ¼ÄÅ«µÄ»¯Ñ§³É·ÖÑо¿ Î¾§;Ê·º£Ã÷;êÃçæ;ÁõÑÞ·¼;ÖÜÓêºç;³ÂÓñƽ;ÍÀÅô·É Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . indole-3-carboxylic acid ÏàËÆ¶È:77.7% The Journal of Antibiotics 2001 54 628-634 TMC-205 a New Transcriptional Up-Regulator of SV40 Promoter Produced by an Unidentified Fungus. Fermentation, Isolation, Physico-chemical Properties, Structure Determination and Biological Activities MASAAKI SAKURAI,JUN KOHNO,MAKI NISHIO,KOZO YAMAMOTO,TORU OKUDA,KIMIO KAWANO and NORIYUKI NAKANISHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . indole-3-carboxylic acid ÏàËÆ¶È:77.7% Zeitschrift f¨¹r Naturforschung C 2011 66 485-490 Effects of Indole Amides on Lettuce and Onion Germination and Growth T. F. Borgati and M. A. D. Boaventura Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . indole-3-carboxylic acid C9H7NO2 ÏàËÆ¶È:77.7% Plant Diversity and Resources 2012 34 101-106 New Withanolides from Nicandra physaloides (Solanaceae) YI Qian-Kun, LI Bo, LIU Ji-Kai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . indole-3-carboxylic acid ÏàËÆ¶È:77.7% The Journal of Organic Chemistry 1996 61 6591-6593 Arthrichitin. A New Cell Wall Active Metabolite from Arthrinium phaeospermum E. K. S. Vijayakumar, Kirity Roy, Sugata Chatterjee, S. K. Deshmukh, and B. N. Ganguli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . indole-3-carboxylic acid C9H7NO2 ÏàËÆ¶È:77.7% Natural Product Research 2013 27 1366-1371 A new 20-membered macrolide produced by a marine-derived Micromonospora strain Peng Fei, Wang Chuan-xi, Xie Yang, Jiang Hong-lei, Chen Lu-jie, Paulina Uribe, Alan T. Bull, Michael Goodfellow, Jiang Hong & Lian Yun-yang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . ßÅßá-3-¼×Ëá ÏàËÆ¶È:77.7% Chinese Journal of Medicinal Chemistry 2012 22 38-43 Chemical constituents from the endophyte Bacillus pumilus derived from Breynia fruticosa HUO Pei-yuan; CHEN Hua-hong; JIANG Yi; HAN Li; XU Li-hua; HUANG Xue-shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . indole ÏàËÆ¶È:75% Journal of Natural Products 1986 Vol 49 534 3-Dimethyallylindole: an Antibacterial and Antifungal Metabolite from Monodora tenuifolia A. O. Adeoye, B. O. Oguntimein, A. M. Clark, C. D. Hufford Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 3-ßÅßá¼×Ëá C9H7O2N ÏàËÆ¶È:75% Chinese Traditional and Herbal Drugs 2010 41 1075-1078 ëҶºÏ»¶µÄ»¯Ñ§³É·Ö ÕÅÄÛÁá;ºú½Ãç;ÁõÓñÇå;ÖÜ¿¡;ÕÔÓÑÐË Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 3,3'-biindole C16H12N2 ÏàËÆ¶È:75% The Journal of Antibiotics 2010 63 681-683 1H,1¡äH-[3,3¡ä]biindolyl from the terrestrial fungus Gliocladium catenulatum Brenda V Bertinetti, M Alejandra Rodriguez, Alicia M Godeas and Gabriela M Cabrera Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 1H-indole-3-carboxylic acid ÏàËÆ¶È:75% Journal of Shenyang Pharmaceutical University 2011 28 938-946 Isolation and identification of the secondary metabolites from marine actinomycete KSC2-1 CAO, Guo-xiu, CHEN, Gang, XU, Wen-feng, WU, Hong-hua, PEI, Yue-hu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . compound 3n C19H18N2 ÏàËÆ¶È:70% Indian Journal of Chemistry Section B 2008 47B 1402-1406 A mild and versatile synthesis of bis(indolyl)methanes and tris(indolyl)alkanes catalyzed by antimony trichloride Kundu,Pradip; Maiti,Gourhari Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 3-[1-(1H-indol-3yl)methyl]-1-methylethyl]-1H-indole C19H18N2 ÏàËÆ¶È:70% Indian Journal of Chemistry Section B 2007 46B 669-673 Efficient synthesis of bis(indolyl) methanes in aqueous medium catalyzed by molybdenyl acetylacetonate Banerjee,B; Mandal,S K; Roy,S C Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . ßÅßá-3-¼×Ëá¼×õ¥ C10H9O2N ÏàËÆ¶È:70% Journal of Shenyang Pharmaceutical University 2009 26 964-967 Chemical constituents of aerial parts of Asarum heterotropides Fr. Schmidt var. mandshuricum (Maxim.)Kitaga. (2) XU Lei, WU Di, WU Zhao-hua, LV Shuai, GAO Hui-yuan, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 3,3'-(ethane-1,1-diyl)bis(1H-indole) C18H16N2 ÏàËÆ¶È:70% Tetrahedron 2013 69 1600-1605 TFA-catalyzed C¨CN bond activation of enamides with indoles: efficient synthesis of 3,3-bisindolylpropanoates and other bisindolylalkanes Hai-Yan Xu, You Zi, Xiao-Ping Xu, Shun-Yi Wang, Shun-Jun Ji Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . ¦Â-indole carboxylic acid ÏàËÆ¶È:66.6% Journal of China Pharmaceutical University 2007 38 315-319 Chemical constituents of the aerial parts of Euphorbia sororia ZHANG Wei-ku; ZHANG Xiao-qi; YE Wen-cai; Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 3-Indolethiocarboxamide C9H8N2S2 ÏàËÆ¶È:66.6% Phytochemistry 2011 72 199-206 Detoxification of cruciferous phytoalexins in Botrytis cinerea: Spontaneous dimerization of a camalexin metabolite M. Soledade C. Pedras, Sajjad Hossain, Ryan B. Snitynsky Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . quindoline ÏàËÆ¶È:62.5% Planta Medica 1996 62 22-27 In Vitro Biological Activities of Alkaloids from Cryptolepis sanguinolenta Kanyanga Cimanga, TessDeBruyne. AleidisLasure, Bart Van Poel, Luc Pieters, Magda Claeys. Dirk VandenBerghe. Kabangu Kambu, Lutete Tona, andArnoldi Vlietinck Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 16-epiaffinine ÏàËÆ¶È:62.5% Journal of Natural Products 1985 Vol 48 571-580 Chemistry of the Annonaceae, Part 18. Benzylated Indoles and Dihydrochalcones in Uvaria angolensis from Tanzania Ilias Muhammad, Peter G. Waterman Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . compound 4 ÏàËÆ¶È:62.5% Canadian Journal of Chemistry 2010 88 548-555 The dehydrogenation of combined organic and inorganic hydrogen-storage carriers Dominik Wechsler, Boyd Davis, and Philip G. Jessop Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 2-cyano-3-nitroimidazoimidazo[1,2-a]pyridine ÏàËÆ¶È:62.5% Journal of Heterocyclic Chemistry 2006 43 565-569 Some nucleophilic substitutions in 2-cyano-3-nitroimidazo[1,2-a]pyridine Lucina Arias,H¨¦actor Salgado-Zamora,Elena Campos,Alicia Reyes,Humberto Cervantes and Edward C. Taylor Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 1H-dibenzo[2,3:6,7]oxepino[4,5-d]imidazole C15H11N2O ÏàËÆ¶È:62.5% Journal of Heterocyclic Chemistry 2010 47 640-656 Novel tetracyclic imidazole derivatives: Synthesis, dynamic NMR study, and anti-inflammatory evaluation Renata Rupčić, Marina Modrić, Antun Hutinec, Ana Čikoš, Barbara Stanić, Milan Mesić, Dijana Pešić and Mladen Merćep Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . Compound 2 C20H9Cl2N3O2 ÏàËÆ¶È:62.5% Bioorganic & Medicinal Chemistry Letters 1992 2 449-452 Preparation of synthons for the synthesis of protein kinase C inhibitors from rebeccamycin. Serge Fabre, Michelle Prudhomme, Maryse Rapp Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . Compound 4 ÏàËÆ¶È:62.5% Bioorganic & Medicinal Chemistry Letters 1995 5 3079-3084 Aromatic guanyl hydrazones: Synthesis, structural studies and in vitro activity against Trypanosoma cruzi J. C. Messeder, L. W. Tinoco, J. D. Figueroa-Villar, E. M. Souza, R. Santa Rita and, S. L. de Castro Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-11-02 10:47:49














»Ø¸´´ËÂ¥