Logo do repositório
 
Publicação

Design, synthesis and stability of N-acyloxymethyl- and N-aminocarbonyloxymethyl-2-azetidinones as human leukocyte elastase inhibitors

dc.contributor.authorClemente, A
dc.contributor.authorDomingos, A
dc.contributor.authorGrancho, AP
dc.contributor.authorIley, J
dc.contributor.authorMoreira, R
dc.contributor.authorNeres, J
dc.contributor.authorPalma, N
dc.contributor.authorSantana, AB
dc.contributor.authorValente, E
dc.date.accessioned2015-12-30T10:17:38Z
dc.date.available2015-12-30T10:17:38Z
dc.date.issued2001
dc.description.abstractA series of N-acyloxymethyl- and N-aminocarbonyloxymethyl derivatives of 2-azetidinones. 3, with different substituent patterns at the beta -lactam C-3 and C-4 positions, were designed as potential mechanism-based inhibitors for human leukocyte elastase and found to exhibit inhibitory potency and selectivity for the enzyme, (C) 2001 Elsevier Science Ltd. All rights reserved.
dc.formatapplication/pdf
dc.identifier.citationBIOORGANIC & MEDICINAL CHEMISTRY LETTERS. - Vol. 11, n. 8 (APR 23 2001), p. 1065-1068
dc.identifier.issn0960-894X
dc.identifier.urihttp://hdl.handle.net/10451/21168
dc.language.isoeng
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD
dc.subjectChemistry, Medicinal
dc.subjectChemistry, Organic
dc.titleDesign, synthesis and stability of N-acyloxymethyl- and N-aminocarbonyloxymethyl-2-azetidinones as human leukocyte elastase inhibitors
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage1068por
oaire.citation.startPage1065por
oaire.citation.titleBIOORGANIC & MEDICINAL CHEMISTRY LETTERSpor
oaire.citation.volumeVol. 11por
rcaap.rightsrestrictedAccess
rcaap.typearticle

Ficheiros