| ²é¿´: 315 | »Ø¸´: 1 | ||
qiupingdafoгæ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú16 ÒÑÓÐ1È˲ÎÓë
|
|
ÈܼÁ£ºë®´úDMSO 107.34,112.14,115.61,120.54,120.91,122.08,125.97,132.20,132.43,136.93,165.89 |
» ²ÂÄãϲ»¶
ר˶310Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
081700»¯Ñ§¹¤³ÌÓë¼¼Êõ Ò»Ö¾Ô¸Öк£Ñó 323 Çóµ÷¼ÁѧУ
ÒѾÓÐ14È˻ظ´
085600£¬321·ÖÇóµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸¶«±±´óѧ085901ÍÁľר˶345Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸¹þ¶û±õ¹¤Òµ´óѧ085600Ó¢Ò»Êý¶þ337·ÖÇóµ÷¼Á
ÒѾÓÐ9È˻ظ´
¹¤¿Æ11408£¬314Çóµ÷¼Á£¬ÓÐÏîÄ¿¾Ñ飬Á˽âtransformer£¬ÄÜѵÁ·Ä£ÐÍ¡£
ÒѾÓÐ3È˻ظ´
348·Ö»·¾³¹¤³Ì¡¤µ÷¼Á
ÒѾÓÐ11È˻ظ´
359Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
0703Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
Ò»Ö¾Ô¸0817»¯Ñ§¹¤³ÌÓë¼¼Êõ£¬Çóµ÷¼Á
ÒѾÓÐ26È˻ظ´
ÌìÑý»¯Ñ§
½ð³æ (³õÈëÎÄ̳)
- Ó¦Öú: 3 (Ó×¶ùÔ°)
- ½ð±Ò: 750.5
- Ìû×Ó: 15
- ÔÚÏß: 25.5Сʱ
- ³æºÅ: 3663865
- ×¢²á: 2015-01-26
- רҵ: ÖÐÒ©Ïû»¯ÓëºôÎüÒ©Àí
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
qiupingdafo(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+10, ok 2015-04-26 12:28:11
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
qiupingdafo(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+10, ok 2015-04-26 12:28:11
|
1 . 1H-indole-3-carboxylic acid ÏàËÆ¶È:81.8% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . ßÅßá-3-¼×Ëá¼×õ¥ C10H9O2N ÏàËÆ¶È:81.8% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . indole-3-carboxylic acid ÏàËÆ¶È:81.8% The Journal of Antibiotics 2008 61 75-80 Studies on Terpenoids Produced by Actinomycetes Keiichiro Motohashi, Kiyofumi Irie, Takashi Toda, Yoshihide Matsuo, Hiroaki Kasai, Masayuki Sue, Kazuo Furihata and Haruo Seto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . indole-3-carboxylic acid ÏàËÆ¶È:81.8% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . indole-3-carboxylic acid ÏàËÆ¶È:81.8% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . indole-3-carboxylic acid C9H7NO2 ÏàËÆ¶È:81.8% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . ¦Â-indole carboxylic acid ÏàËÆ¶È:81.8% Military Medical Sciences 2013 37 279-282 Chemical constituents from Solanum lyratum Thunb£®£¨¢ò£© YIN Hai-long, LI Jian, DONG Jun-xing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ßÅßá-3-¼×Ëá ÏàËÆ¶È:81.8% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 1H-Indole-3-carboxylic acid ÏàËÆ¶È:81.8% Journal of Qingdao University of Science and Technology (Natural Science Edition) 2007 28 502-504 Studies on the Chemical Constituents of the Marine Sponge (Xetospongia testudinaria) from the South China Sea GUO Sen-hui, ZHONG Hui-min, LIN Wen-han Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Â-indole carboxylic acid ÏàËÆ¶È:81.8% Bulletin of the Academy of Military Medical Sciences 2013 37 279-282 Chemical constituents from Solanum lyratum Thunb. ( ¢ò) YIN Hai-long, LI Jian, DONG Jun-xing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . indolyl-3-carboxylic acid C9H7NO2 ÏàËÆ¶È:72.7% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 1H-ßÅßá-2-ôÈËá ÏàËÆ¶È:72.7% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . indole-3-carboxylic acid ÏàËÆ¶È:72.7% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . indole-3-carboxylic acid C9H7NO2 ÏàËÆ¶È:72.7% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . indole-3-carboxylic acid ÏàËÆ¶È:72.7% Chinese Traditional and Herbal Drugs 2014 45 631-634 Chemical constituents from seeds of Helianthus annuus FEI Yong-he, CHEN Zhong, LI Xiao-ran, XU Qiong-ming, YANG Shi-lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . indole-3-carboxylic acid ÏàËÆ¶È:72.7% Chinese Traditional and Herbal Drugs 2015 46 344−347 Chemical constituents from pods of Glycine max ZHANG-Meng, XU Qiong-ming, WANG Tao-yun, YANG Shi-lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 1H-indole-3-carboxylic acid, methyl ester ÏàËÆ¶È:72.7% Chinese Traditional and Herbal Drugs 2015 46 334−338 Chemical constituents from shoots of Phyllostachys edulis (I) DU Wen-peng, XU Peng, LIU Bo, XU Xiang-hong, LAI Xue-wen, LI Bin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . ¦Â-carboline ÏàËÆ¶È:63.6% Journal of Natural Products 1997 60 802-803 Secondary Metabolites from the Sponge Tedania anhelans: Isolation and Characterization of Two Novel Pyrazole Acids and Other Metabolites P. S. Parameswaran, C. G. Naik, and Vinod R. Hegde Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . 1,3-dihydro-1,3,3-tris(trifluoromethyl)isobenzofuran-1-ol C11H5F9O2 ÏàËÆ¶È:63.6% Helvetica Chimica Acta 2008 91 97−110 A One-Pot Synthesis of 1,3-Dihydro-1,3,3-tris(perfluoroalkyl)isobenzofuran-1-olates and Their Complete NMR Spectroscopic Analysis on the Basis of 1D and 2D Experiments Wieland Tyrra, Harald Scherer, Lesya A. Babadzhanova, Natalya V. Kirij, Yurii L. Yagupolskii, Dieter Naumann, and Ingo Pantenburg Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . Zn(NHQuin-H)2•2H2O ZnC22H20N2O8 ÏàËÆ¶È:63.6% Journal of Heterocyclic Chemistry 2003 40 645-648 Novel ¡®quinolone' metal complexes: Synthesis and spectroscopic studies of mg(II),zn(II) and ba(II) complexes with N-methyl (or NH)-3-acetyl-4-hydroxy quinolin-2-one ligands Giorgos Athanasellis,Efstathios Gavrielatos,Olga Igglessi-Markopoulou and John Markopoulos Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . bis(3-indolyl) ketone C17H12N2O ÏàËÆ¶È:63.6% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . k1-Methyl-1H-indole-3-thiocarboxamide ÏàËÆ¶È:63.6% Bioorganic & Medicinal Chemistry Letters 2002 12 2317-2320 A Practical Synthesis of 3,4-Diethoxybenzthioamide Based on Friedel¨CCrafts Reaction with Potassium Thiocyanate in Methanesulfonic Acid Shinji Aki, Takafumi Fujioka, Masashi Ishigami, Jun-ichi Minamikawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . Compound 1 C13H17N2 ÏàËÆ¶È:63.6% Bioorganic & Medicinal Chemistry Letters 2003 13 4481-4483 Conicamin, a novel histamine antagonist from the mediterranean tunicate Aplidium conicum Anna Aiello, Francesca Borrelli, Raffaele Capasso, Ernesto Fattorusso, Paolo Luciano, Marialuisa Menna Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . 3-ßÅßá¼×Ëá C9H7O2N ÏàËÆ¶È:63.6% Chinese Traditional and Herbal Drugs 2010 41 1075-1078 ëҶºÏ»¶µÄ»¯Ñ§³É·Ö ÕÅÄÛÁá;ºú½Ãç;ÁõÓñÇå;ÖÜ¿¡;ÕÔÓÑÐË Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 25 . 1-hydroxy-2,3-bis(3-indolyl)-3-pyrrolin-2,5-dione C20H13N3O3 ÏàËÆ¶È:63.6% The Journal of Antibiotics 1995 48 863-868 Antimicrobial Activities of Indolocarbazole and Bis-indole Protein Kinase C Inhibitors II. Substitution on Maleimide Nitrogen with Functional Groups Bearing a Labile Hydrogen ELISABETE RODRIGUES PEREIRA, SERGE FABRE, MARTINE SANCELME, MICHELLE PRUDHOMME, MARYSE RAPP Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 26 . 3-(1H-pyrazol-4-yl)-1H-indole C11H9N3 ÏàËÆ¶È:63.6% Tetrahedron 2013 69 5829-5840 Preparation of indole containing building blocks for the regiospecific construction of indole appended pyrazoles and pyrroles John T. Gupton, Nakul Telang, Dominic F. Gazzo, Peter J. Barelli, Kristin E. Lescalleet, Jonathan W. Fagan, Brandon J. Mills, Kara L. Finzel, Rene P.F. Kanters, Kyle R. Crocker, Sean T. Dudek, Corinne M. Lariviere, Stanton Q. Smith, Kartik M. Keertikar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 27 . 3-Indolethiocarboxamide C9H8N2S2 ÏàËÆ¶È:63.6% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 28 . cyclobrassinin sulfoxide C11H10N2OS2 ÏàËÆ¶È:63.6% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 29 . 1H-ßÅßò C7H6N2 ÏàËÆ¶È:63.6% Asia-Pacific Traditional Medicine 2013 9 47-48 ´óÀöÂÖУ¾ú´Î¼¶´úл²úÎïÑо¿ CUI Xiu-chun, LUO Du-qiang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 30 . 9H-pyrido[2,3-b]indol-2-amine ÏàËÆ¶È:63.6% Chemical Research in Toxicology 1997 10 1192-1197 Identification of the Major Hepatic DNA Adduct Formed by the Food Mutagen 2-Amino-9H-pyrido[2,3-b]indole (A¦ÁC) Wolfgang Pfau, Christian Schulze, Tomoyuki Shirai, Rhyohei Hasegawa, and Ulrike Brockstedt Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 31 . (E)-5-Bromo-3-(2-nitrovinyl)-1H-indole ÏàËÆ¶È:63.6% Marine Drugs 2013 11 1427-1439 Total Synthesis and Biological Activity of Marine Alkaloid Eudistomins Y1¨CY7 and Their Analogues Huijuan Jin, Puyong Zhang, Krikor Bijian, Sumei Ren, Shengbiao Wan, Moulay A. Alaoui-Jamali and Tao Jiang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 32 . 1H-indole-3-carboxylic acid ÏàËÆ¶È:63.6% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 33 . N-(1H-indole-3-carbonyl)urea ÏàËÆ¶È:63.6% Helvetica Chimica Acta 1994 77 1886-1894 Imidazolone and Imidazolidinone Artifacts of a Pivotal Imidazolthione, Zyzzin, from the poecilosclerid sponge Zyzza massalis from the coral sea. The first thermochromic systems of marine origin Ines Mancini, Graziano Guella, Francesco Pietra, C¨¦cile Debitus and Daniel Duhet Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 34 . 1H-indole-3-carboxylic acid ÏàËÆ¶È:63.6% Marine Sciences 2009 33 81-86 Chemical constituents of EN-22, an endophytic fungus derived from the marine red alga Polysiphonia urceolata ZHAO Ting-ting, LI Xiao-ming, LI Jing-mei, LI Ke, CUI Chuan-ming, LI Chun-shun, WANG Bin-gui Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 35 . N-[3,5-Bis(trifluoromethyl)phenyl]-2,4-dinitrobenzenesulfonamide C14H7F6N3O6S ÏàËÆ¶È:63.6% Monatshefte f¨¹r Chemie 2013 144 461-471 Electron-withdrawing substituted benzenesulfonamides against the predominant community-associated methicillin-resistant Staphylococcus aureus strain USA300 Wanida Phetsang, Soraya Chaturongakul, Chutima Jiarpinitnun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 36 . 3-(hydroxyacetyl)indole ÏàËÆ¶È:63.6% China Journal of Chinese Materia Medica 2014 39 3777-3781 Studies on chemical Constituents from cultivated Gynura nepalensis LU Yao, LI Zhi-hong, MA Lin, DENG An-jun, WU Feng, ZHANG Zhi-hui, QIN Hai-lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 37 . 3-(hydroxyacetyl)indole C10H9NO2 ÏàËÆ¶È:63.6% Chinese Traditional and Herbal Drugs 2014 45 1367-1372 Chemical constituents from roots of Sambucus williamsii (I) YANG Bing-you, SONG Dan-dan, HAN Hua, YANG Liu, LIU Yan, WANG Qiu-hong, KUANG Hai-xue Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 38 . ethyl 1H-indole-3-carboxylate C11H11NO2 ÏàËÆ¶È:63.6% Molecules 2014 19 20695-20708 Photochemistry of Benzotriazoles: Generation of 1,3-Diradicals and Intermolecular Cycloaddition as a New Route toward Indoles and Dihydropyrrolo[3,4-b]Indoles Nader A. Al-Jalal, Maher R. Ibrahim, Nouria A. Al-Awadi, Mohamed H. Elnagdi and Yehia A. Ibrahim Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 39 . 2-(4-chloro-3-methylphenoxy)-N'-[{5'-(4-bromophenyl)-furan-2'-yl}-methylidene]-acetohydrazide C20H16ClN2O3Br ÏàËÆ¶È:63.6% Medicinal Chemistry Research 2014 23 4050−4059 Synthesis and evaluation of 2-(2-((4-substituted-phenoxy)methyl)-1H-benzo[d] imidazol-1-yl)acetohydrazone derivatives as antitumor agents Zicheng Li, Sicheng Zhang, Lei Deng, Jing Hu, Huan Li, Yinglan Zhao, Youfu Luo, Wencai Huang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 40 . 2-(4-chloro-3-methylphenoxy)-N'-[{5'-(4-carboxyphenyl)-furan-2'-yl}-methylidene]-acetohydrazide C21H17ClN2O5 ÏàËÆ¶È:63.6% Medicinal Chemistry Research 2014 23 4050−4059 Synthesis and evaluation of 2-(2-((4-substituted-phenoxy)methyl)-1H-benzo[d] imidazol-1-yl)acetohydrazone derivatives as antitumor agents Zicheng Li, Sicheng Zhang, Lei Deng, Jing Hu, Huan Li, Yinglan Zhao, Youfu Luo, Wencai Huang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 41 . compound 9b ÏàËÆ¶È:61.5% Natural Product Research 1994 5 225-232 Synthesis of 1-(¦Â-indolyl)1,3-butadienes, Yuehchukene and Analogues, and Murrapanine via Acid-catalyzed Reactions of ¦Â-(1-hydroxybut-3-enyl)indoles Yua-Kuang Chen; Huey-Fen Chung; Jyh-Horng Sheu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 42 . (Z)-2-benzylidenebenzofuran-3(2H)-one C15H10O2 ÏàËÆ¶È:61.5% Journal of the Chemical Society, Perkin Transactions 1 1981 3182-3185 Analysis of the Tautomeric Structures of Auronols by 13C N.m.r. and Comparison with the Isomeric Flavonols By Andrew Pelter and Robert S. Ward,Rudolf Hansel and Faies Khaliefi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 43 . compound 11 ÏàËÆ¶È:61.5% Journal of the Chemical Society, Perkin Transactions 1 1981 3182-3185 Analysis of the tautomeric structures of auronols by 13C n.m.r. and comparison with the isomeric flavonols Andrew Pelter, Robert S. Ward, Rudolf Hänsel and Faies Khaliefi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 44 . 2-(2-Furyl)-3-(4-methoxyphenyl)thieno[3,2-b]pyridin-7(4H)-one C18H13NO3S ÏàËÆ¶È:61.5% Synthesis 2014 46 3319−3330 A Convenient and Efficient Synthesis of 2-(Het)arylthieno[3,2-b]pyridin-7(4H)-ones and 2,3-Di(het)arylthieno[3,2-b]pyridin-7(4H)-ones Puvvala, Srinu; Jadhav, Vinod D.; Farooq, Sheikh M.; Reddy, C. Venkata Ramana; Machiraju, Pavan Kumar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 45 . 5-Nitro-3,6-dihydropyrazolo[3,4-c]carbazole C13H8N4O2 ÏàËÆ¶È:61.5% Bioorganic & Medicinal Chemistry 2013 21 4102-4111 Identification of 1,6-dihydropyrazolo[4,3-c]carbazoles and 3,6-dihydropyrazolo[3,4-c]carbazoles as new Pim kinase inhibitors Virginie Suchaud, Laurent Gavara, Emmanuelle Saugues, Lionel Nauton, Vincent Th¨¦ry, Fabrice Anizon, Pascale Moreau Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-04-02 10:44:08














»Ø¸´´ËÂ¥