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pubmed-article:9873718pubmed:abstractTextInterfacial peptides of HIV-1 protease were crosslinked with varying length alkyl-chains containing either a single cis or trans double bond, or a triple bond to remove degrees of freedom within the tethers. The synthesis of these compounds and their effects on the activity of HIV-1 protease are described.lld:pubmed
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pubmed-article:9873718pubmed:authorpubmed-author:ChmielewskiJJlld:pubmed
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pubmed-article:9873718pubmed:articleTitleRestricting the flexibility of crosslinked, interfacial peptide inhibitors of HIV-1 protease.lld:pubmed
pubmed-article:9873718pubmed:affiliationDepartment of Chemistry, Purdue University, West Lafayette, IN 47907, USA.lld:pubmed
pubmed-article:9873718pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9873718pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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