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dc.contributor.authorCunico, Wilson
dc.contributor.authorFerreira, Maria de Lourdes G
dc.contributor.authorWardell, James L.
dc.contributor.authorHarrison, William T A
dc.date.accessioned2017-07-17T14:00:18Z
dc.date.available2017-07-17T14:00:18Z
dc.date.issued2017-06-01
dc.identifier.citationCunico , W , Ferreira , M D L G , Wardell , J L & Harrison , W T A 2017 , ' Different intra- and inter-molecular hydrogen-bonding patterns in (3S,4aS,8aS)-2-[(2R,3S)-3-(2,5-X2-benzamido)-2-(2,5-X2-benzo-yloxy)-4-phenyl-butyl]-N-tert-butyldeca-hydro-iso-quinoline-3-carboxamides (X = H or Cl) : compounds with moderate aspartyl protease inhibition activity ' Acta Crystallographica Section E Crystallographic Communications , vol 73 , no. Pt 6 , pp. 913-917 . DOI: 10.1107/S2056989017007800en
dc.identifier.issn2056-9890
dc.identifier.otherPURE: 102524511
dc.identifier.otherPURE UUID: da2d271e-6b93-44c4-a9d2-d2ed60542d22
dc.identifier.otherPubMed: 28638658
dc.identifier.otherPubMedCentral: PMC5458323
dc.identifier.otherScopus: 85020263662
dc.identifier.urihttp://hdl.handle.net/2164/8964
dc.descriptionWe thank the EPSRC National Crystallography Service (University of Southampton) for the X-ray data collections.en
dc.format.extent5en
dc.language.isoeng
dc.relation.ispartofActa Crystallographica Section E Crystallographic Communicationsen
dc.rightsJournal policy: the journal is open access Open-access licence: Creative Commons Attribution (CC-BY) https://creativecommons.org/licenses/by/3.0/en
dc.subjectcrystal structureen
dc.subjectmalariaen
dc.subjectiso-quinolinecarboxamideen
dc.subjectHydrogen Bondingen
dc.subjectaspartyl protease inhibition activityen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleDifferent intra- and inter-molecular hydrogen-bonding patterns in (3S,4aS,8aS)-2-[(2R,3S)-3-(2,5-X2-benzamido)-2-(2,5-X2-benzo-yloxy)-4-phenyl-butyl]-N-tert-butyldeca-hydro-iso-quinoline-3-carboxamides (X = H or Cl) : compounds with moderate aspartyl protease inhibition activityen
dc.typeJournal articleen
dc.contributor.institutionUniversity of Aberdeen, Natural & Computing Sciences, Chemistryen
dc.description.statusPeer revieweden
dc.description.versionPublisher PDFen
dc.identifier.doihttp://dx.doi.org/10.1107/S2056989017007800


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