Literature DB >> 9871560

Synthesis and 5 alpha-reductase inhibitory activities of benzofuran derivatives with a carbamoyl group.

K Ishibashi1, K Nakajima, Y Sugioka, M Sugiyama, T Hamada, H Horikoshi, T Nishi.   

Abstract

A series of 2-phenylbenzofuran derivatives with a diphenylmethylcarbamoyl group at the 5 or 6 position of the benzofuran ring were synthesized and evaluated for rat and human testosterone 5 alpha-reductase inhibitory activities in vitro. They had inhibitory activities against both enzymes and the 6-carbamoyl derivatives tended to be more potent than the 5-carbamoyl compounds.

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Year:  1998        PMID: 9871560     DOI: 10.1016/s0960-894x(98)00001-8

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

1.  Synthesis of New 2-Arylbenzo[b]furan Derivatives via Palladium-Catalyzed Suzuki Cross-Coupling Reactions in Aqueous Media.

Authors:  Qianqian Chen; Panli Jiang; Mengping Guo; Jianxin Yang
Journal:  Molecules       Date:  2018-09-25       Impact factor: 4.411

  1 in total

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