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Triacylglycerols Based on 2-(N-tert-Butoxycarbonylamino)oleic Acid Are Potent Inhibitors of Pancreatic Lipase

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dc.contributor.author Magrioti, V en
dc.contributor.author Verger, R en
dc.contributor.author Constantinou-Kokotou, V en
dc.date.accessioned 2014-06-06T06:46:10Z
dc.date.available 2014-06-06T06:46:10Z
dc.date.issued 2004 en
dc.identifier.issn 00222623 en
dc.identifier.uri http://dx.doi.org/10.1021/jm034202s en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/2818
dc.subject.other 2 (n tert butoxycarbonylamino)oleic acid en
dc.subject.other 2 methylglycerol en
dc.subject.other enzyme inhibitor en
dc.subject.other oleic acid en
dc.subject.other triacylglycerol en
dc.subject.other triacylglycerol lipase en
dc.subject.other triolein en
dc.subject.other unclassified drug en
dc.subject.other aqueous solution en
dc.subject.other article en
dc.subject.other drug structure en
dc.subject.other drug synthesis en
dc.subject.other enzyme inhibition en
dc.subject.other hydrolysis en
dc.subject.other surface tension en
dc.subject.other Humans en
dc.subject.other Lipase en
dc.subject.other Oleic Acids en
dc.subject.other Pancreas en
dc.subject.other Stomach en
dc.subject.other Structure-Activity Relationship en
dc.subject.other Triglycerides en
dc.title Triacylglycerols Based on 2-(N-tert-Butoxycarbonylamino)oleic Acid Are Potent Inhibitors of Pancreatic Lipase en
heal.type journalArticle en
heal.identifier.primary 10.1021/jm034202s en
heal.publicationDate 2004 en
heal.abstract A novel class of potent human pancreatic lipase (HPL) inhibitors was developed. Triacylglycerol analogues containing 2-(N-tert-butoxycarbonylamino) fatty acids were synthesized, and their ability to form stable films at the air/ water interface was studied. The inhibition of human digestive lipases by the compounds synthesized was studied by the monolayer technique, and the triesters of glycerol and 2-methylglycerol with 2-(N-tert-butoxycarbonylamino)oleic acid were found to be potent inhibitors of HPL. en
heal.journalName Journal of Medicinal Chemistry en
dc.identifier.issue 2 en
dc.identifier.volume 47 en
dc.identifier.doi 10.1021/jm034202s en
dc.identifier.spage 288 en
dc.identifier.epage 291 en


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