タイトル | Design, synthesis, and biological and structural evaluations of novel HIV-1 protease inhibitors to combat drug resistance. |
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ジャーナル・号・ページ | J. Med. Chem., Vol. 55, Page 6328-6341, Year 2012 |
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掲載日 | 2012年2月2日 (構造データの登録日) |
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著者 | Parai, M.K. / Huggins, D.J. / Cao, H. / Nalam, M.N. / Ali, A. / Schiffer, C.A. / Tidor, B. / Rana, T.M. |
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リンク | J. Med. Chem. / PubMed:22708897 |
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手法 | X線回折 |
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解像度 | 1.4 - 1.78 Å |
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構造データ | PDB-4djo: Crystal Structure of wild-type HIV-1 Protease in Complex with MKP56 手法: X-RAY DIFFRACTION / 解像度: 1.78 Å PDB-4djp: Crystal Structure of wild-type HIV-1 Protease in Complex with MKP73 手法: X-RAY DIFFRACTION / 解像度: 1.4 Å PDB-4djq: Crystal Structure of wild-type HIV-1 Protease in Complex with MKP86 手法: X-RAY DIFFRACTION / 解像度: 1.4 Å PDB-4djr: Crystal Structure of wild-type HIV-1 Protease in Complex with MKP97 手法: X-RAY DIFFRACTION / 解像度: 1.55 Å |
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化合物 | ChemComp-MK5: 2-[(dichloroacetyl)amino]ethyl [(2S,3R)-3-hydroxy-4-{[(4-methoxyphenyl)sulfonyl][(2S)-2-methylbutyl]amino}-1-phenylbutan-2-yl]carbamate
ChemComp-M73: methyl (2S)-3-({[(2S,3R)-3-hydroxy-4-{[(4-methoxyphenyl)sulfonyl][(2S)-2-methylbutyl]amino}-1-phenylbutan-2-yl]carbamoyl}oxy)-2-methylpropanoate
ChemComp-M86: 2-(2-oxoimidazolidin-1-yl)ethyl [(2S,3R)-3-hydroxy-4-{[(4-methoxyphenyl)sulfonyl][(2S)-2-methylbutyl]amino}-1-phenylbutan-2-yl]carbamate
ChemComp-0KJ: [(2S)-5-oxopyrrolidin-2-yl]methyl [(2S,3R)-4-{(1,3-benzothiazol-6-ylsulfonyl)[(2S)-2-methylbutyl]amino}-3-hydroxy-1-phenylbutan-2-yl]carbamate
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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 | HYDROLASE/HYDROLASE inhibitor / HIV-1 protease / drug resistance / drug design / Protease inhibitors / AIDS / Aspartyl protease / HYDROLASE-HYDROLASE inhibitor complex |
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