Literature DB >> 9063086

Quantitative structure-activity relationship (QSAR) study of polyhydroxyxanthones.

J Ungwitayatorn1, M Pickert, A W Frahm.   

Abstract

In the present study 13C-chemical shift additivity rules are developed for polyhydroxyxanthones with antituberculotic activity against Mycobacterium tuberculosis. QSAR investigations are performed by correlating 13C-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.

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Year:  1997        PMID: 9063086     DOI: 10.1016/s0031-6865(96)00043-x

Source DB:  PubMed          Journal:  Pharm Acta Helv        ISSN: 0031-6865


  2 in total

Review 1.  New small-molecule synthetic antimycobacterials.

Authors:  Lluis Ballell; Robert A Field; Ken Duncan; Robert J Young
Journal:  Antimicrob Agents Chemother       Date:  2005-06       Impact factor: 5.191

2.  Cytotoxic Xanthones from Hypericum stellatum, an Ethnomedicine in Southwest China.

Authors:  Yuanyuan Ji; Ruifei Zhang; Chen Zhang; Xingyu Li; Adam Negrin; Chaonan Yuan; Edward J Kennelly; Chunlin Long
Journal:  Molecules       Date:  2019-10-02       Impact factor: 4.411

  2 in total

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