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Title | Design and Synthesis of Potent HIV-1 Protease Inhibitors Containing Bicyclic Oxazolidinone Scaffold as the P2 Ligands: Structure-Activity Studies and Biological and X-ray Structural Studies. |
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Journal, issue, pages | J. Med. Chem., Vol. 61, Page 9722-9737, Year 2018 |
Publish date | Jul 26, 2018 (structure data deposition date) |
Authors | Ghosh, A.K. / Williams, J.N. / Ho, R.Y. / Simpson, H.M. / Hattori, S.I. / Hayashi, H. / Agniswamy, J. / Wang, Y.F. / Weber, I.T. / Mitsuya, H. |
External links | J. Med. Chem. / PubMed:30354121 |
Methods | X-ray diffraction |
Resolution | 1.22 - 1.3 Å |
Structure data | PDB-6e7j: PDB-6e9a: |
Chemicals | ChemComp-HWY: ChemComp-NA: ChemComp-CL: ChemComp-HOH: ChemComp-J0S: ChemComp-FMT: |
Source |
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Keywords | HYDROLASE/HYDROLASE INHIBITOR / ANTIVIRAL / HIV-1 PROTEASE INHIBITOR OF GRL-042-17A / P2 LIGAND / MULTIDRUG-RESISTANT / OXAZOLIDINONE / VIRAL PROTEIN / HYDROLASE-HYDROLASE INHIBITOR complex / HIV-1 PROTEASE INHIBITOR OF GRL-034-17A / HYDROLASE |