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Title | Design, Synthesis and X-Ray Structural Studies of Potent HIV-1 Protease Inhibitors Containing C-4 Substituted Tricyclic Hexahydro-Furofuran Derivatives as P2 Ligands. |
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Journal, issue, pages | Chemmedchem, Vol. 17, Page e202200058-e202200058, Year 2022 |
Publish date | Jan 23, 2022 (structure data deposition date) |
![]() | Ghosh, A.K. / Kovela, S. / Sharma, A. / Shahabi, D. / Hopkins, D.R. / Yadav, M. / Johnson, M.E. / Agniswamy, J. / Wang, Y.F. / Hattori, S.I. ...Ghosh, A.K. / Kovela, S. / Sharma, A. / Shahabi, D. / Hopkins, D.R. / Yadav, M. / Johnson, M.E. / Agniswamy, J. / Wang, Y.F. / Hattori, S.I. / Higashi-Kuwata, N. / Aoki, M. / Amano, M. / Weber, I.T. / Mitsuya, H. |
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Methods | X-ray diffraction |
Resolution | 1.13 - 1.21 Å |
Structure data | ![]() PDB-7to5: ![]() PDB-7to6: |
Chemicals | ![]() ChemComp-NA: ![]() ChemComp-CL: ![]() ChemComp-FMT: ![]() ChemComp-G8R: ![]() ChemComp-GOL: ![]() ChemComp-HOH: ![]() ChemComp-G77: ![]() ChemComp-ACT: |
Source |
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![]() | ANTIVIRAL PROTEIN/INHIBITOR / ASPARTIC ACID PROTEASE / HIV-1 PROTEASE / INHIBITORS / ANTIVIRAL PROTEIN / ANTIVIRAL PROTEIN-INHIBITOR complex / VIRAL PROTEIN/INHIBITOR / SPARTIC ACID PROTEASE / VIRAL PROTEIN / VIRAL PROTEIN-INHIBITOR complex |