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Published in 2017 at "Bioorganic chemistry"
DOI: 10.1016/j.bioorg.2017.01.006
Abstract: A novel series of substituted N-(2-(2,3-dioxoindolin-1-yl)acetyl)-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxamide was designed, synthesized and evaluated for in vitro Reverse Transcriptase (RT) inhibitory activity. This series is a combination of peculiar structural features from leading scaffolds of [(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT) and…
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Keywords:
isatin hybrids;
hybrids novel;
reverse;
reverse transcriptase ... See more keywords