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Volumn 14, Issue 4, 2004, Pages 909-912

Design and synthesis of 3,7-diarylimidazopyridines as inhibitors of the VEGF-receptor KDR

Author keywords

[No Author keywords available]

Indexed keywords

IMIDAZOPYRIDINE DERIVATIVE; PROTEIN TYROSINE KINASE; PROTEIN TYROSINE KINASE INHIBITOR; VASCULOTROPIN RECEPTOR;

EID: 10744233313     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2003.12.007     Document Type: Article
Times cited : (49)

References (20)
  • 4
    • 0034648765 scopus 로고    scopus 로고
    • For reviews, see:
    • For reviews, see: Carmeliet P., Jain R.K. Nature. 407:2000;249.
    • (2000) Nature , vol.407 , pp. 249
    • Carmeliet, P.1    Jain, R.K.2
  • 17
    • 85030909950 scopus 로고    scopus 로고
    • note
    • 1H NMR and mass spectroscopy.
  • 18
    • 0033525530 scopus 로고    scopus 로고
    • 50 value represents biochemical inhibition of phosphorylation of a poly-Glu/Tyr (4:1) peptide substrate by isolated KDR kinase (cloned and expressed as a GST-fusion protein), see: Values are reported as single determinations or as the average of at least two determinations±standard deviation
    • 50 value represents biochemical inhibition of phosphorylation of a poly-Glu/Tyr (4:1) peptide substrate by isolated KDR kinase (cloned and expressed as a GST-fusion protein), see: Kendall R.L., Rutledge R.Z., Mao X., Tebben A.L., Hungate R.W., Thomas K.A. J. Biol. Chem. 274:1999;6453. Values are reported as single determinations or as the average of at least two determinations±standard deviation.
    • (1999) J. Biol. Chem. , vol.274 , pp. 6453
    • Kendall, R.L.1    Rutledge, R.Z.2    Mao, X.3    Tebben, A.L.4    Hungate, R.W.5    Thomas, K.A.6
  • 19
    • 85030910755 scopus 로고    scopus 로고
    • Compounds 10f and 10g were prepared similarly according to the following Scheme
    • Compounds 10f and 10g were prepared similarly according to the following Scheme:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.