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Volumn 20, Issue 14, 2010, Pages 4156-4158

Structure-based design and synthesis of pyrrole derivatives as MEK inhibitors

Author keywords

MEK; Oncology; Pyrrole

Indexed keywords

PYRROLE DERIVATIVE;

EID: 77953872377     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2010.05.058     Document Type: Article
Times cited : (59)

References (20)
  • 13
    • 77953873630 scopus 로고    scopus 로고
    • note
    • m ATP concentration indicated compounds were not ATP competitive inhibitors.
  • 14
    • 77953873203 scopus 로고    scopus 로고
    • note
    • 50s generated for all compounds listed were at a minimum 50-fold higher in the PC3 cell line.
  • 15
    • 77953873569 scopus 로고    scopus 로고
    • Full experimental procedures for compounds 13-26 are contained within the following patent application: Adams, M. E, Dong, Q, Kaldor, S. W, Kanouni, T, Wallace, M. B. PCT Int. Patent Appl. WO 08/055236, 2008
    • Full experimental procedures for compounds 13-26 are contained within the following patent application: Adams, M. E.; Dong, Q.; Kaldor, S. W.; Kanouni, T.; Wallace, M. B. PCT Int. Patent Appl. WO 08/055236, 2008.
  • 18
    • 77953870347 scopus 로고    scopus 로고
    • note
    • Kinase Panel: Abl1, AKT3, c-RAF, CamK1Δ, CDK2/cyclinA, cMet, cSRC, EGFR, GSK3β, IR, JAK3, P38α, PDGFRβ, PDK1, PKCα, PLK3, Syk, Tie2.
  • 19
    • 77953871076 scopus 로고    scopus 로고
    • note
    • Compounds were administered intravenously and orally at 1 and 5 mg/kg, respectively.
  • 20
    • 77953871700 scopus 로고    scopus 로고
    • note
    • Protein Data Bank code is 3MBL.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.