Publication:
Quantitative structure-activity relationship (QSAR) study of polyhydroxyxanthones

dc.contributor.authorJ. Ungwitayatornen_US
dc.contributor.authorM. Pickerten_US
dc.contributor.authorA. W. Frahmen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUniversitat Freiburg im Breisgauen_US
dc.date.accessioned2018-07-04T07:40:50Z
dc.date.available2018-07-04T07:40:50Z
dc.date.issued1997-02-01en_US
dc.description.abstractIn the present study13C-chemical shift additivity rules are developed for polyhydroxyxanthones with antituberculotic activity against Mycobacterium tuberculosis. QSAR investigations are performed by correlating13C-chemical shifts and calculated dipole moments of several 1,3-substituted polyhydroxyxanthones with their antituberculotic activity and by using the CoMFA approach as a three-dimensional QSAR method.en_US
dc.identifier.citationPharmaceutica Acta Helvetiae. Vol.72, No.1 (1997), 23-29en_US
dc.identifier.doi10.1016/S0031-6865(96)00043-Xen_US
dc.identifier.issn00316865en_US
dc.identifier.other2-s2.0-0031047390en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/17902
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0031047390&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleQuantitative structure-activity relationship (QSAR) study of polyhydroxyxanthonesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0031047390&origin=inwarden_US

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