<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>66(6)</volume><submitter>Diamond TL</submitter><funding>Merck</funding><pubmed_abstract>Islatravir (ISL) is a nucleoside reverse transcriptase translocation inhibitor (NRTTI) that inhibits human immunodeficiency virus (HIV) reverse transcription by blocking reverse transcriptase (RT) translocation on the primer:template. ISL is being developed for the treatment of HIV-1 infection. To expand our knowledge of viral variants that may confer reduced susceptibility to ISL, resistance selection studies were conducted with wild-type (WT) subtype A, B, and C viruses. RT mutations encoding M184I and M184V were the most frequently observed changes. Selection studies were also initiated with virus containing a single known resistance-associated mutation in RT (K65R, L74I, V90I, M184I, or M184V), and no additional mutations were observed. Antiviral activity assays were performed on varia</pubmed_abstract><journal>Antimicrobial agents and chemotherapy</journal><pagination>e0013322</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9211433</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Islatravir Has a High Barrier to Resistance and Exhibits a Differentiated Resistance Profile from Approved Nucleoside Reverse Transcriptase Inhibitors (NRTIs).</pubmed_title><pmcid>PMC9211433</pmcid><pubmed_authors>Xu M</pubmed_authors><pubmed_authors>Lai MT</pubmed_authors><pubmed_authors>Diamond TL</pubmed_authors><pubmed_authors>Ngo W</pubmed_authors><pubmed_authors>Grobler JA</pubmed_authors><pubmed_authors>Rodriguez S</pubmed_authors><pubmed_authors>Goh SL</pubmed_authors><pubmed_authors>Asante-Appiah E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Islatravir Has a High Barrier to Resistance and Exhibits a Differentiated Resistance Profile from Approved Nucleoside Reverse Transcriptase Inhibitors (NRTIs).</name><description>Islatravir (ISL) is a nucleoside reverse transcriptase translocation inhibitor (NRTTI) that inhibits human immunodeficiency virus (HIV) reverse transcription by blocking reverse transcriptase (RT) translocation on the primer:template. ISL is being developed for the treatment of HIV-1 infection. To expand our knowledge of viral variants that may confer reduced susceptibility to ISL, resistance selection studies were conducted with wild-type (WT) subtype A, B, and C viruses. RT mutations encoding M184I and M184V were the most frequently observed changes. Selection studies were also initiated with virus containing a single known resistance-associated mutation in RT (K65R, L74I, V90I, M184I, or M184V), and no additional mutations were observed. Antiviral activity assays were performed on varia</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jun</publication><modification>2026-06-15T05:45:20.349Z</modification><creation>2025-04-22T16:34:36.353Z</creation></dates><accession>S-EPMC9211433</accession><cross_references><pubmed>35546110</pubmed><doi>10.1128/aac.00133-22</doi></cross_references></HashMap>