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Chromene-Containing Aromatic Sulfonamides with Carbonic Anhydrase Inhibitory Properties.
Angeli, Andrea; Kartsev, Victor; Petrou, Anthi; Pinteala, Mariana; Brovarets, Volodymyr; Slyvchuk, Sergii; Pilyo, Stepan; Geronikaki, Athina; Supuran, Claudiu T.
Afiliação
  • Angeli A; Neuro Farba Department, Sezione di Scienze Farmaceutiche, Università degli Studi di Firenze, Via Ugo Schiff 6, Sesto Fiorentino, 50019 Florence, Italy.
  • Kartsev V; Centre of Advanced Research in Bionanoconjugates and Biopolymers, Petru Poni Institute of Macromolecular Chemistry, Aleea Grigore Ghica-Voda, No. 41A, 700487 Iasi, Romania.
  • Petrou A; InterBioScreen, Chernogolovka 142432, Moscow Region, Russia.
  • Pinteala M; Department of Pharmacy, School of Health, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
  • Brovarets V; Centre of Advanced Research in Bionanoconjugates and Biopolymers, Petru Poni Institute of Macromolecular Chemistry, Aleea Grigore Ghica-Voda, No. 41A, 700487 Iasi, Romania.
  • Slyvchuk S; Department of Chemistry of Bioactive Nitrogen-Containing Heterocyclic Bases, V.P. Kukhar Institute of Bioorganic Chemistry and Petrochemistry, NAS of Ukraine 1, Murmanska St, 02094 Kyiv, Ukraine.
  • Pilyo S; Department of Chemistry of Bioactive Nitrogen-Containing Heterocyclic Bases, V.P. Kukhar Institute of Bioorganic Chemistry and Petrochemistry, NAS of Ukraine 1, Murmanska St, 02094 Kyiv, Ukraine.
  • Geronikaki A; Department of Chemistry of Bioactive Nitrogen-Containing Heterocyclic Bases, V.P. Kukhar Institute of Bioorganic Chemistry and Petrochemistry, NAS of Ukraine 1, Murmanska St, 02094 Kyiv, Ukraine.
  • Supuran CT; Department of Pharmacy, School of Health, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
Int J Mol Sci ; 22(10)2021 May 11.
Article em En | MEDLINE | ID: mdl-34064890
Carbonic anhydrases (CAs, EC 4.2.1.1) catalyze the essential reaction of CO2 hydration in all living organisms, being actively involved in the regulation of a plethora of patho/physiological conditions. A series of chromene-based sulfonamides were synthesized and tested as possible CA inhibitors. Their inhibitory activity was assessed against the cytosolic human isoforms hCA I, hCA II and the transmembrane hCA IX and XII. Several of the investigated derivatives showed interesting inhibition activity towards the tumor associate isoforms hCA IX and hCA XII. Furthermore, computational procedures were used to investigate the binding mode of this class of compounds, within the active site of hCA IX.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sulfonamidas / Benzopiranos / Inibidores da Anidrase Carbônica / Anidrases Carbônicas Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sulfonamidas / Benzopiranos / Inibidores da Anidrase Carbônica / Anidrases Carbônicas Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article