<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>51(10)</volume><submitter>Blair WS</submitter><pubmed_abstract>More than 10(6) compounds were evaluated in a human immunodeficiency virus type 1 (HIV-1) high-throughput antiviral screen, resulting in the identification of a novel HIV-1 inhibitor (UK-201844). UK-201844 exhibited antiviral activity against HIV-1 NL4-3 in MT-2 and PM1 cells, with 50% effective concentrations of 1.3 and 2.7 microM, respectively, but did not exhibit measurable antiviral activity against the closely related HIV-1 IIIB laboratory strain. UK-201844 specifically inhibited the production of infectious virions packaged with an HIV-1 envelope (Env), but not HIV virions packaged with a heterologous Env (i.e., the vesicular stomatitis virus glycoprotein), suggesting that the compound targets HIV-1 Env late in infection. Subsequent antiviral assays using HIV-1 NL4-3/IIIB chimeric vi</pubmed_abstract><journal>Antimicrobial agents and chemotherapy</journal><pagination>3554-61</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2043256</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Identification and characterization of UK-201844, a novel inhibitor that interferes with human immunodeficiency virus type 1 gp160 processing.</pubmed_title><pmcid>PMC2043256</pmcid><pubmed_authors>Patick AK</pubmed_authors><pubmed_authors>Cao J</pubmed_authors><pubmed_authors>Blair WS</pubmed_authors><pubmed_authors>Malfait AM</pubmed_authors><pubmed_authors>Butler SL</pubmed_authors><pubmed_authors>Wu H</pubmed_authors><pubmed_authors>Graham J</pubmed_authors><pubmed_authors>Chu A</pubmed_authors><pubmed_authors>Jimenez J</pubmed_authors><pubmed_authors>Isaacson J</pubmed_authors><pubmed_authors>Tortorella M</pubmed_authors><pubmed_authors>Peng Q</pubmed_authors><pubmed_authors>Jackson L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification and characterization of UK-201844, a novel inhibitor that interferes with human immunodeficiency virus type 1 gp160 processing.</name><description>More than 10(6) compounds were evaluated in a human immunodeficiency virus type 1 (HIV-1) high-throughput antiviral screen, resulting in the identification of a novel HIV-1 inhibitor (UK-201844). UK-201844 exhibited antiviral activity against HIV-1 NL4-3 in MT-2 and PM1 cells, with 50% effective concentrations of 1.3 and 2.7 microM, respectively, but did not exhibit measurable antiviral activity against the closely related HIV-1 IIIB laboratory strain. UK-201844 specifically inhibited the production of infectious virions packaged with an HIV-1 envelope (Env), but not HIV virions packaged with a heterologous Env (i.e., the vesicular stomatitis virus glycoprotein), suggesting that the compound targets HIV-1 Env late in infection. Subsequent antiviral assays using HIV-1 NL4-3/IIIB chimeric vi</description><dates><release>2007-01-01T00:00:00Z</release><publication>2007 Oct</publication><modification>2025-06-01T01:12:08.711Z</modification><creation>2019-03-27T02:21:48Z</creation></dates><accession>S-EPMC2043256</accession><cross_references><pubmed>17646410</pubmed><doi>10.1128/aac.00643-07</doi><doi>10.1128/AAC.00643-07</doi></cross_references></HashMap>