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Discovery of curcumin inspired sulfonamide derivatives as a new class of carbonic anhydrase isoforms I, II, IX, and XII inhibitors.

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Title: Discovery of curcumin inspired sulfonamide derivatives as a new class of carbonic anhydrase isoforms I, II, IX, and XII inhibitors.
Authors: Ramya PVS; a Department of Medicinal Chemistry , National Institute of Pharmaceutical Education and Research (NIPER) , Hyderabad , India., Angapelly S; a Department of Medicinal Chemistry , National Institute of Pharmaceutical Education and Research (NIPER) , Hyderabad , India., Angeli A; b NEUROFARBA Department , Università degli Studi di Firenze, Sezione di Scienze Farmaceutiche , Florence , Italy., Digwal CS; a Department of Medicinal Chemistry , National Institute of Pharmaceutical Education and Research (NIPER) , Hyderabad , India., Arifuddin M; a Department of Medicinal Chemistry , National Institute of Pharmaceutical Education and Research (NIPER) , Hyderabad , India., Babu BN; a Department of Medicinal Chemistry , National Institute of Pharmaceutical Education and Research (NIPER) , Hyderabad , India., Supuran CT; b NEUROFARBA Department , Università degli Studi di Firenze, Sezione di Scienze Farmaceutiche , Florence , Italy., Kamal A; a Department of Medicinal Chemistry , National Institute of Pharmaceutical Education and Research (NIPER) , Hyderabad , India.
Source: Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2017 Dec; Vol. 32 (1), pp. 1274-1281.
Publication Type: Journal Article
Journal Info: Publisher: Taylor & Francis Country of Publication: England NLM ID: 101150203 Publication Model: Print Cited Medium: Internet ISSN: 1475-6374 (Electronic) Linking ISSN: 14756366 NLM ISO Abbreviation: J Enzyme Inhib Med Chem Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Discovery of curcumin inspired sulfonamide derivatives as a new class of carbonic anhydrase isoforms I, II, IX, and XII inhibitors.
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  Data: <searchLink fieldCode="AU" term="%22Ramya+PVS%22">Ramya PVS</searchLink>; a Department of Medicinal Chemistry , National Institute of Pharmaceutical Education and Research (NIPER) , Hyderabad , India.<br /><searchLink fieldCode="AU" term="%22Angapelly+S%22">Angapelly S</searchLink>; a Department of Medicinal Chemistry , National Institute of Pharmaceutical Education and Research (NIPER) , Hyderabad , India.<br /><searchLink fieldCode="AU" term="%22Angeli+A%22">Angeli A</searchLink>; b NEUROFARBA Department , Università degli Studi di Firenze, Sezione di Scienze Farmaceutiche , Florence , Italy.<br /><searchLink fieldCode="AU" term="%22Digwal+CS%22">Digwal CS</searchLink>; a Department of Medicinal Chemistry , National Institute of Pharmaceutical Education and Research (NIPER) , Hyderabad , India.<br /><searchLink fieldCode="AU" term="%22Arifuddin+M%22">Arifuddin M</searchLink>; a Department of Medicinal Chemistry , National Institute of Pharmaceutical Education and Research (NIPER) , Hyderabad , India.<br /><searchLink fieldCode="AU" term="%22Babu+BN%22">Babu BN</searchLink>; a Department of Medicinal Chemistry , National Institute of Pharmaceutical Education and Research (NIPER) , Hyderabad , India.<br /><searchLink fieldCode="AU" term="%22Supuran+CT%22">Supuran CT</searchLink>; b NEUROFARBA Department , Università degli Studi di Firenze, Sezione di Scienze Farmaceutiche , Florence , Italy.<br /><searchLink fieldCode="AU" term="%22Kamal+A%22">Kamal A</searchLink>; a Department of Medicinal Chemistry , National Institute of Pharmaceutical Education and Research (NIPER) , Hyderabad , India.
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  Data: <searchLink fieldCode="JN" term="%22101150203%22">Journal of enzyme inhibition and medicinal chemistry</searchLink> [J Enzyme Inhib Med Chem] 2017 Dec; Vol. 32 (1), pp. 1274-1281.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Taylor+%26+Francis%22">Taylor & Francis </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101150203 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1475-6374 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2214756366%22">14756366 </searchLink><i>NLM ISO Abbreviation: </i>J Enzyme Inhib Med Chem <i>Subsets: </i>MEDLINE
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        Value: 10.1080/14756366.2017.1380638
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        Text: English
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      – TitleFull: Discovery of curcumin inspired sulfonamide derivatives as a new class of carbonic anhydrase isoforms I, II, IX, and XII inhibitors.
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            NameFull: Ramya PVS
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            – D: 01
              M: 12
              Text: 2017 Dec
              Type: published
              Y: 2017
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