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Design, synthesis and biological evaluation of novel acetamide-substituted doravirine and its prodrugs as potent HIV-1 NNRTIs.
- Source :
-
Bioorganic & Medicinal Chemistry . Feb2019, Vol. 27 Issue 3, p447-456. 10p. - Publication Year :
- 2019
-
Abstract
- Graphical abstract Abstract A novel series of acetamide-substituted derivatives and two prodrugs of doravirine were designed and synthesized as potent HIV-1 NNRTIs by employing the structure-based drug design strategy. In MT-4 cell-based assays using the MTT method, it was found that most of the new compounds exhibited moderate to excellent inhibitory potency against the wild-type (WT) HIV-1 strain with a minimum EC 50 value of 54.8 nM. Among them, the two most potent compounds 8i (EC 50 = 59.5 nM) and 8k (EC 50 = 54.8 nM) displayed robust activity against WT HIV-1 with double-digit nanomolar EC 50 values, being superior to lamivudine (3TC, EC 50 = 12.8 μM) and comparable to doravirine (EC 50 = 13 nM). Besides, 8i and 8k shown moderate activity against the double RT mutant (K103N + Y181C) HIV-1 RES056 strain. The HIV-1 RT inhibition assay further validated the binding target. Molecular simulation of the representative compounds was employed to provide insight on their structure-activity relationships (SARs) and direct future design efforts. Finally, the aqueous solubility and chemical stability of the prodrugs 9 and 10 were investigated in detail. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 09680896
- Volume :
- 27
- Issue :
- 3
- Database :
- Academic Search Index
- Journal :
- Bioorganic & Medicinal Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 134150883
- Full Text :
- https://doi.org/10.1016/j.bmc.2018.12.039