메뉴 건너뛰기




Volumn 15, Issue 7, 2005, Pages 1857-1861

Structure-based design, synthesis, and biological evaluation of novel 1,4-diazepines as HDM2 antagonists

Author keywords

Cancer; Diazepine; HDM2 p53; Selenium

Indexed keywords

5 [3 (4 CHLOROPHENYL) 4 [1 (4 CHLOROPHENYL)ETHYL] 2,5 DIOXO 7 PHENYL 1,4 DIAZEPIN 1 YL]VALERIC ACID; 5 [7 (2 BROMOPHENYL) 3 (4 CHLOROPHENYL) 4 [1 (4 CHLOROPHENYL)ETHYL] 2,5 DIOXO 1,4 DIAZEPIN 1 YL]VALERIC ACID; DIAZEPINE DERIVATIVE; UNCLASSIFIED DRUG; VALERIC ACID DERIVATIVE;

EID: 20144382874     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2005.02.018     Document Type: Article
Times cited : (51)

References (23)
  • 8
    • 0030941458 scopus 로고    scopus 로고
    • A.J. Levine Cell 88 3 1997 323 331
    • (1997) Cell , vol.88 , Issue.3 , pp. 323-331
    • Levine, A.J.1
  • 14
    • 85030807963 scopus 로고    scopus 로고
    • note
    • d = 20 nM), 50 mM Hepes pH 7.5, 150 mM NaCl, 3 mM β-octyl glucopyranoside, and 2.5% DMSO. Compound, HDM2 and peptide were incubated for 15-20 min at room temperature prior to reading the fluorescence polarization (excitation = 485 nM, emission = 530 nM)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.