The structure-based design, synthesis, and biological evaluation of a series of nonpeptidic HIV-1 protease inhibitors with rationally designed P2â² ligands are described. The inhibitors are designed to enhance backbone binding interactions, particularly at the S2â² subsite. Synthesis of inhibitors was carried out efficiently. The stereochemistry of alcohol functionalities of the P2â² ligands was set by asymmetric reduction of the corresponding ketone using (R,R)- or (S,S)-Noyori catalysts. A number of inhibitors displayed very potent enzyme inhibitory and antiviral activity. Inhibitors 3g and 3h showed enzyme Kivalues of 27.9 and 49.7 pm and antiviral activity of 6.2 and 3.9 nm, respectively. These inhibitors also remained quite potent against darunavir-resistant HIV-1 variants. An X-ray structure of inhibitor 3g in complex with HIV-1 protease revealed key interactions in the S2â² subsite.
Ghosh, A.K., Fyvie, W.S., Brindisi, M., Steffey, M., Agniswamy, J., Wang, Y., et al. (2017). Design, Synthesis, Biological Evaluation, and X‐ray Studies of HIV‐1 Protease Inhibitors with Modified P2′ Ligands of Darunavir. CHEMMEDCHEM, 12(23), 1942-1952 [10.1002/cmdc.201700614].
Design, Synthesis, Biological Evaluation, and X‐ray Studies of HIV‐1 Protease Inhibitors with Modified P2′ Ligands of Darunavir
Brindisi, Margherita;
2017-01-01
Abstract
The structure-based design, synthesis, and biological evaluation of a series of nonpeptidic HIV-1 protease inhibitors with rationally designed P2â² ligands are described. The inhibitors are designed to enhance backbone binding interactions, particularly at the S2â² subsite. Synthesis of inhibitors was carried out efficiently. The stereochemistry of alcohol functionalities of the P2â² ligands was set by asymmetric reduction of the corresponding ketone using (R,R)- or (S,S)-Noyori catalysts. A number of inhibitors displayed very potent enzyme inhibitory and antiviral activity. Inhibitors 3g and 3h showed enzyme Kivalues of 27.9 and 49.7 pm and antiviral activity of 6.2 and 3.9 nm, respectively. These inhibitors also remained quite potent against darunavir-resistant HIV-1 variants. An X-ray structure of inhibitor 3g in complex with HIV-1 protease revealed key interactions in the S2â² subsite.File | Dimensione | Formato | |
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https://hdl.handle.net/11365/1030065