Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/6789
DC FieldValueLanguage
dc.contributor.authorGhosh, Arun K.en_us
dc.contributor.authorFyvie, W. Seanen_us
dc.contributor.authorBrindisi, Margheritaen_us
dc.contributor.authorSteffey, Melindaen_us
dc.contributor.authorAgniswamy, Johnsonen_us
dc.contributor.authorWang, Yuan-Fangen_us
dc.contributor.authorAoki, Manabuen_us
dc.contributor.authorAmano, Masayukien_us
dc.contributor.authorWeber, Irene T.en_us
dc.contributor.authorMitsuya, Hiroakien_us
dc.date.accessioned2021-03-30T16:05:56Z-
dc.date.available2021-03-30T16:05:56Z-
dc.date.issued2017-
dc.identifier.issn1860-7179en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12779/6789-
dc.description126209en_US
dc.language.isoenen_US
dc.relationNoneen_US
dc.relation.ispartofCHEMMEDCHEMen_US
dc.subjectdrug resistance; HIV-1 protease inhibitors; P2â ² ligands; pharmacokinetics; structure-based design; Crystallography, X-Ray; Darunavir; HIV Protease; HIV Protease Inhibitors; Ligands; Models, Molecular; Molecular Conformation; Structure-Activity Relationship; Drug Design; Molecular Medicine; Pharmacology, Toxicology and Pharmaceutics (all); Organic Chemistryen_US
dc.titleDesign, Synthesis, Biological Evaluation, and X‐ray Studies of HIV‐1 Protease Inhibitors with Modified P2′ Ligands of Darunaviren_US
dc.typeArticleen_US
dc.identifier.doi10.1002/cmdc.201700614en_US
dc.identifier.pmid29110408en_US
dc.identifier.scopus2-s2.0-85034983571en_US
dc.identifier.isiWOS:000417492400008en_US
dc.identifier.urlhttp://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1860-7187en_US
dc.relation.volume12en_US
dc.relation.issue23en_US
dc.description.firstpage1942en_US
dc.description.lastpage1952en_US
dc.description.thirdmissionNot applicableen_US
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeArticle-
item.fulltextNo Fulltext-
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