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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. |
|---|---|
| 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 |
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human immunodeficiency virus 1
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