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Volumn 48, Issue 3, 2000, Pages 382-388

A novel class of inhibitors for human steroid 5α-reductase: Synthesis and biological evaluation of indole derivatives. II

Author keywords

5 reductase inhibitor; Benign prostatic hypertrophy; Indole derivative; YM 32906

Indexed keywords

3 CHLORO 4 [[1 (4 PHENOXYBENZYL) 1H INDOL 5 YL]OXY]BENZOIC ACID; 4 [(1 BENZYL 1H INDOL 5 YL)OXY] 3 CHLOROBENZOIC ACID; FINASTERIDE; INDOLE DERIVATIVE; STEROID 5ALPHA REDUCTASE INHIBITOR; UNCLASSIFIED DRUG;

EID: 0034071008     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.48.382     Document Type: Article
Times cited : (9)

References (27)
  • 14
    • 4243760426 scopus 로고
    • Eur. Patent Appl., EP 291245
    • Recent studies on nonsteroidal 5α-reductase inhibitors: a) Nakai H., Terajima H., Arai Y., Eur. Patent Appl., EP 291245 [Chem. Abstr., 110, 212384t (1989)];
    • (1989) Chem. Abstr. , vol.110
    • Nakai, H.1    Terajima, H.2    Arai, Y.3
  • 24
    • 0342768368 scopus 로고    scopus 로고
    • note
    • The inhibitory activities of finasteride and (±)-ONO-3805 for human prostatic 5α-reductase were evaluated in our company. The results are described in Table 4.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.