| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10596384 | Bioorganic & Medicinal Chemistry Letters | 2009 | 5 Pages |
Abstract
A novel class of tetrahydro-pyrazinopyrimidine-2-carboxamides have been identified as HIV-1 integrase inhibitors. Optimization of the initial lead culminated in the discovery of a series of compounds with high potency on the enzyme and an antiviral cell-based activity equivalent to that showed by Raltegravir, the first in class HIV-1 integrase inhibitor.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Alessia Petrocchi, Philip Jones, Michael Rowley, Fabrizio Fiore, Vincenzo Summa,
![First Page Preview: N-(4-Fluorobenzyl)-3-hydroxy-9,9-dimethyl-4-oxo-6,7,8,9-tetrahydro-4H-pyrazino[1,2-a]pyrimidine-2-carboxamides a novel class of potent HIV-1 integrase inhibitors N-(4-Fluorobenzyl)-3-hydroxy-9,9-dimethyl-4-oxo-6,7,8,9-tetrahydro-4H-pyrazino[1,2-a]pyrimidine-2-carboxamides a novel class of potent HIV-1 integrase inhibitors](/preview/png/10596384.png)