Literature DB >> 12790343

Quantitative structure-activity relationships of carbonic anhydrase inhibitors.

Satya P Gupta1.   

Abstract

A review is presented of quantitative structure-activity relationships (QSARs) of different categories of carbonic anhydrase (CA) inhibitors, which are basically benzenesulfonamides, heterocyclic sulfonamides and aliphatic sulfonamides. The review shows that in all categories, the inhibition potency depends largely on the electronic properties of the sulfonamide group, which can be affected by the electronic characteristics of the substituents present on the nucleus (benzene or heterocyclic ring) of the sulfonamide molecules. Substituents themselves can be involved, along with the nucleus, in some dispersion interaction with the enzyme. Based on this review, a schematic model is presented to represent the interaction of sulfonamides with the CA.

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Year:  2003        PMID: 12790343     DOI: 10.1007/978-3-0348-8012-1_6

Source DB:  PubMed          Journal:  Prog Drug Res        ISSN: 0071-786X


  3 in total

Review 1.  Carbonic anhydrase as a model for biophysical and physical-organic studies of proteins and protein-ligand binding.

Authors:  Vijay M Krishnamurthy; George K Kaufman; Adam R Urbach; Irina Gitlin; Katherine L Gudiksen; Douglas B Weibel; George M Whitesides
Journal:  Chem Rev       Date:  2008-03       Impact factor: 60.622

2.  Stabilization of anionic and neutral forms of a fluorophoric ligand at the active site of human carbonic anhydrase I.

Authors:  Sumathra Manokaran; Jayati Banerjee; Sanku Mallik; D K Srivastava
Journal:  Biochim Biophys Acta       Date:  2010-07-08

3.  Discovery of novel SERCA inhibitors by virtual screening of a large compound library.

Authors:  Christopher Elam; Michael Lape; Joel Deye; Jodie Zultowsky; David T Stanton; Stefan Paula
Journal:  Eur J Med Chem       Date:  2011-02-25       Impact factor: 6.514

  3 in total

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