| タイトル | Cyclic urea amides: HIV-1 protease inhibitors with low nanomolar potency against both wild type and protease inhibitor resistant mutants of HIV. |
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| ジャーナル・号・ページ | J. Med. Chem., Vol. 40, Page 181-191, Year 1997 |
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| 掲載日 | 1997年4月25日 (構造データの登録日) |
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著者 | Jadhav, P.K. / Ala, P. / Woerner, F.J. / Chang, C.H. / Garber, S.S. / Anton, E.D. / Bacheler, L.T. |
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リンク | J. Med. Chem. / PubMed:9003516 |
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| 手法 | X線回折 |
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| 解像度 | 1.8 - 2.1 Å |
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| 構造データ | PDB-1qbr: HIV-1 PROTEASE INHIBITORS WIIH LOW NANOMOLAR POTENCY 手法: X-RAY DIFFRACTION / 解像度: 1.8 Å PDB-1qbt: HIV-1 PROTEASE INHIBITORS WIIH LOW NANOMOLAR POTENCY 手法: X-RAY DIFFRACTION / 解像度: 2.1 Å PDB-1qbu: HIV-1 PROTEASE INHIBITORS WIIH LOW NANOMOLAR POTENCY 手法: X-RAY DIFFRACTION / 解像度: 1.8 Å |
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| 化合物 | ChemComp-XV6: [4R-(4ALPHA,5ALPHA,6BETA,7BETA)]-3,3'-[[TETRAHYDRO-5,6-DIHYDROXY-2-OXO-4,7-BIS(PHENYLMETHYL)-1H-1,3-DIAZEPINE-1,3(2H)-D / XV-638
ChemComp-146: [4R-(4ALPHA,5ALPHA,6ALPHA,7ALPHA)]-3,3'-{{TETRAHYDRO-5,6-DIHYDROXY-2-OXO-4,7-BIS(PHENYLMETHYL)-1H-1,3-DIAZEPINE-1,3(2H)-DIYL]BIS(METHYLENE)]BIS[N-1H-BENZIMIDAZOL-2-YLBENZAMIDE] / SD-146
ChemComp-846: [4R--(1ALPHA,5ALPHA,7BETA)]-3-[(CYCLOPROPHYLMETHYL)HEXAHYDRO-5,6-DIHYDROXY-2-OXO-4,7-BIS(PHENYLMETHYL)-1H-1,3-DIAZEPIN] / Q-8467
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| 由来 |  human immunodeficiency virus 1 (ヒト免疫不全ウイルス)
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キーワード | ASPARTYL PROTEASE / HYDROLASE (ACID PROTEINASE) |
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