Studies of Human Immunodeficiency Virus Type 1 (HIV-1) Protease Inhibitors. III. Structure-Activity Relationship of HIV-1 Protease Inhibitors Containing Cyclohexylalanylalanine Hydroxyethylene Dipeptide Isostere
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- 桜井 満也
- Exploratory Chemistry Research, Sankyo Co., Ltd.,
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- 東田 勧
- Exploratory Chemistry Research, Sankyo Co., Ltd.,
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- 菅野 真知子
- Exploratory Chemistry Research, Sankyo Co., Ltd.,
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- 半田 宏
- Faculty of Bioscience and Biotechnology, Tokyo Institute of Technology
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- 駒井 知明
- Biological Research Laboratories, Sankyo Co., Ltd.,
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- 八木 隆一
- Biological Research Laboratories, Sankyo Co., Ltd.,
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- 西垣 隆
- Biological Research Laboratories, Sankyo Co., Ltd.,
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- 矢部 裕一郎
- Exploratory Chemistry Research, Sankyo Co., Ltd.,
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Systematic replacement of the P_4-P_2 subsites of substrate-based human immunodeficiency virus type 1 protease (HIV-1 PR) inhibitors containing cyclohexylalanylalanine hydroxyethylene dipeptide isostere (Cha-ψ[H.E.]-Ala) at positions corresponding to the scissile sites of substrates was carried out. The structure-activity relationship revealed that compounds with the combination of hydrophilic P_3 and β-branched hydrophobic P_2 amino acids generally showed strong inhibitory activity against HIV-1 PR. In particular, compounds 4 (Boc-Orn-Val-Cha-ψ[H.E.]-Ala-NHBu^n; Bu^n=n-butyl, K_i=11 nM) and 6 (Z-Orn-Val-Cha-ψ[H.E.]-Ala-NHBu^n, K_i=8 nM) exhibited good enzyme selectivity, possessing no significant inhibitory activities toward closely related aspartic proteases, pepsin, cathepsin D, and renin. As a possible model system for evaluating these compounds, anti-retroviral (anti-Mo-MSV/MLV complex (Mo-MSV=Moloney murine sarcoma virus; MLV=murine leukemia virus)) activity was investigated. Both compounds were found to inhibit moderately the focus formation of Mo-MSV/MLV complex in NIH3T3 cells (compound 4,IC_<50>=1.8 μM; compound 6,IC_<50>= 1.0 μM).
収録刊行物
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- Chem. Pharm. Bull.
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Chem. Pharm. Bull. 42 534-540, 1994
公益社団法人日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1573950402116307712
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- NII論文ID
- 110003630976
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- NII書誌ID
- AA00602100
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- ISSN
- 00092363
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- 本文言語コード
- en
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- データソース種別
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- CiNii Articles