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Volumn 8, Issue 5, 2003, Pages 188-189

Gleevec: Tailoring to fit

(1)  May, Thomas S a  

a NONE

Author keywords

[No Author keywords available]

Indexed keywords

6 (2,6 DICHLOROPHENYL) 2 (4 FLUORO 3 METHYLANILINO) 8 METHYL 8H PYRIDO[2,3 D]PYRIMIDIN 7 ONE; 6 (2,6 DICHLOROPHENYL) 2 [3 (HYDROXYMETHYL)ANILINO] 8 METHYLPYRIDO[2,3 D]PYRIMIDIN 7(8H) ONE; ANTINEOPLASTIC AGENT; IMATINIB; PHOSPHOTRANSFERASE INHIBITOR; PROTEIN TYROSINE KINASE INHIBITOR; UNCLASSIFIED DRUG;

EID: 0037336773     PISSN: 13596446     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1359-6446(03)02615-1     Document Type: Short Survey
Times cited : (6)

References (2)
  • 1
    • 0037115644 scopus 로고    scopus 로고
    • Activity of the Bcr-Abl kinase inhibitor PD180970 against clinically relevant Bcr-Abl isoforms that cause resistance to imatinib mesylate (Gleevec, STI571)
    • La Rosée P., et al. Activity of the Bcr-Abl kinase inhibitor PD180970 against clinically relevant Bcr-Abl isoforms that cause resistance to imatinib mesylate (Gleevec, STI571). Cancer Res. 62:2002;7149-7153.
    • (2002) Cancer Res. , vol.62 , pp. 7149-7153
    • La Rosée, P.1
  • 2
    • 0012907461 scopus 로고    scopus 로고
    • A novel pyridopyrimidine inhibitor of Abl kinase is a picomolar inhibitor of Bcr-abl driven K562 cells and is effective against STI571-resistant Bcr-abl mutants
    • in press
    • Huron, D.R. et al. A novel pyridopyrimidine inhibitor of Abl kinase is a picomolar inhibitor of Bcr-abl driven K562 cells and is effective against STI571-resistant Bcr-abl mutants. Clin. Cancer Res. (in press).
    • Clin. Cancer Res.
    • Huron, D.R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.