Small molecule inhibitors of the LEDGF site of HIV type 1 integrase identified by fragment screening and structure based design
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Small molecule inhibitors of the LEDGF site of HIV type 1 integrase identified by fragment screening and structure based design Descriptor: 5-{[(2-{[bis(4-methoxyphenyl)methyl]carbamoyl}benzyl)(prop-2-en-1-yl)amino]methyl}-1,3-benzodioxole-4-carboxylic acid, ACETIC ACID, INTEGRASE, ... Authors: Peat, T.S, Newman, J, Rhodes, D.I, Deadman, J.J, Vandergraaff, N, Le, G, Jones, E.D, Smith, J.A, Coates, J.A.V, Thienthong, N, Dolezal, O, Ryan, J.H, Savage, G.P, Francis, C.L. Deposit date: 2011-06-30 Release date: 2012-07-11 Last modified: 2023-12-20 Method: X-RAY DIFFRACTION (1.75 Å) Cite: Small Molecule Inhibitors of the Ledgf Site of Human Immunodeficiency Virus Integrase Identified by Fragment Screening and Structure Based Design. Plos One, 7, 2012
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2011-06-30



