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Volumn 43, Issue 7, 2008, Pages 1444-1453

Inhibition of PDGFR tyrosine kinase activity by a series of novel N-(3-(4-(pyridin-3-yl)-1H-imidazol-2-ylamino)phenyl)amides - A SAR study on the bioisosterism of pyrimidine and imidazole

Author keywords

1H Imidazol 2 ylamine; Bioisosterism; PDGFR; Pyrimidine; Receptor tyrosine kinase

Indexed keywords

ANTINEOPLASTIC AGENT; CD135 ANTIGEN; IMATINIB; IMIDAZOLE; N (3 (4 (PYRIDIN 3 YL) 1H IMIDAZOLE 2 YLAMINO)PHENYL)AMIDE DERIVATIVE; PLATELET DERIVED GROWTH FACTOR RECEPTOR; PROTEIN TYROSINE KINASE; PYRIMIDINE;

EID: 45849148111     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2007.09.021     Document Type: Article
Times cited : (9)

References (20)
  • 11
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    • M. Ciufolini, A. Benjahad, B. Giethlen, A. Moussy, C. Wermuth, PCT Int. Appl., WO 2006/064375 A2, 2006.
  • 13
    • 45849099029 scopus 로고    scopus 로고
    • E. Vanotti, R. D'Alessio, M. Tibolla, M. Varasi, A. Montagnoli, C. Santocanale, K. Martina, M. Menichincheri, PCT Int. Appl., WO 2005013986 A1, 2005.
    • E. Vanotti, R. D'Alessio, M. Tibolla, M. Varasi, A. Montagnoli, C. Santocanale, K. Martina, M. Menichincheri, PCT Int. Appl., WO 2005013986 A1, 2005.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.