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contentType Journal Article
endingPage 4332
issn 0960-894X
issueIdentifier 15
pageRange 4328-4332
publicationName Bioorganic & Medicinal Chemistry Letters
startingPage 4328
bibliographicCitation Su DS, Lim JJ, Tinney E, Tucker TJ, Saggar S, Sisko JT, Wan BL, Young MB, Anderson KD, Rudd D, Munshi V, Bahnck C, Felock PJ, Lu M, Lai MT, Touch S, Moyer G, Distefano DJ, Flynn JA, Liang Y, Sanchez R, Perlow-Poehnelt R, Miller M, Vacca JP, Williams TM, Anthony NJ. Biaryl ethers as potent allosteric inhibitors of reverse transcriptase and its key mutant viruses: aryl substituted pyrazole as a surrogate for the pyrazolopyridine motif. Bioorg Med Chem Lett. 2010 Aug 01;20(15):4328–32. doi: 10.1016/j.bmcl.2010.06.083. PMID: 20609585.
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date 2010-08-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://doi.org/10.1016/j.bmcl.2010.06.083
https://pubmed.ncbi.nlm.nih.gov/20609585
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language English
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title Biaryl ethers as potent allosteric inhibitors of reverse transcriptase and its key mutant viruses: Aryl substituted pyrazole as a surrogate for the pyrazolopyridine motif
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Total number of triples: 276.