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Volumn 20, Issue 15, 2010, Pages 4491-4495

Design and synthesis of 4-[3,5-dioxo-11-oxa-4,9-diazatricyclo[5.3.1.0 2,6]undec-4-yl]-2-trifluoromethyl-benzonitriles as androgen receptor antagonists

Author keywords

Androgen receptor; Antagonist; Diazatricycloundecane; Prostate cancer

Indexed keywords

4 [3,5 DIOXO 11 OXA 4,9 DIAZATRICYCLO[5.3.1.0 2,6]UNDEC 4 YL] 2 TRIFLUOROMETHYL BENZONITRILE DERIVATIVE; ANTIANDROGEN; BENZONITRILE; BICALUTAMIDE; FLUTAMIDE; NILUTAMIDE; SEX HORMONE ANTAGONIST; TESTOSTERONE PROPIONATE; UNCLASSIFIED DRUG;

EID: 77955425421     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2010.06.034     Document Type: Article
Times cited : (10)

References (26)
  • 2
    • 10644248039 scopus 로고
    • K.L. Gao Drugs 43 1991 254
    • (1991) Drugs , vol.43 , pp. 254
    • Gao, K.L.1
  • 24
    • 77955413338 scopus 로고    scopus 로고
    • note
    • i) were determined in whole cells measuring displacement by tritiated DHT in the MDA-453 cell line. See Ref. 11 below for experimental details on assays.
  • 26
    • 77955421506 scopus 로고    scopus 로고
    • note
    • For example, the in vitro metabolic stability of compound 37 was evaluated at 3 μM in the presence of human, rat, and mouse liver microsomes. After a 10 min incubation, the % compound remaining for compound 37 in humans, rats, and mice was 76%, 100%, and 92%, respectively.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.