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Volumn 47, Issue 2, 1999, Pages 226-240

Synthesis of 2-phenylbenzofuran derivatives as testosterone 5α- reductase inhibitor

Author keywords

2 phenylbenzofuran; Benign prostatic hyperplasia; Testosterone 5 reductase inhibitor

Indexed keywords

4 [2 [5 [N (4,4' DIMETHOXYDIPHENYLMETHYL)AMINO]BENZO[B]FURAN 2 YL]PHENYLOXY]BUTYRIC ACID; 4 [2 [6 (N DIPHENYLMETHYLAMINO)BENZO[B]FURAN 2 YL]BUTYRIC ACID; STEROID 5ALPHA REDUCTASE INHIBITOR; UNCLASSIFIED DRUG;

EID: 0032963632     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.47.226     Document Type: Article
Times cited : (11)

References (19)
  • 8
    • 4243760426 scopus 로고
    • Ono Pharmaceutical Co., Ltd., EP 0291245 (1988)
    • f) Nakai H., Terashima H., Arai Y., Ono Pharmaceutical Co., Ltd., EP 0291245 (1988) [Chem. Abstr., 110, 212384t (1989)];
    • (1989) Chem. Abstr. , vol.110
    • Nakai, H.1    Terashima, H.2    Arai, Y.3
  • 15
    • 84920310462 scopus 로고    scopus 로고
    • The reaction for 10h under the same reaction condition gave 5-formyl-2-(3-hydroxyphenyl)benzofuran, but the yield was low.
    • The reaction for 10h under the same reaction condition gave 5-formyl-2-(3-hydroxyphenyl)benzofuran, but the yield was low.
  • 18
    • 84920310461 scopus 로고    scopus 로고
    • note
    • u= 0.066. Full X-ray crystallographic data has been deposited with the Cambridge Crystallographic Data Centre.
  • 19
    • 84920310460 scopus 로고    scopus 로고
    • The stable conformations of 44a were estimated using CHARMm/ QUANTA. The structure in which the two methoxy groups were excluded from the X-ray structure of 44c was used as an initial conformation.
    • The stable conformations of 44a were estimated using CHARMm/ QUANTA. The structure in which the two methoxy groups were excluded from the X-ray structure of 44c was used as an initial conformation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.