Carbonic anhydrase inhibitors. Sulfonamide diuretics revisited--old leads for new applications?
Sulfonamide diuretics such as hydrochlorothiazide, hydroflumethiazide, quinethazone, metolazone, chlorthalidone, indapamide, furosemide and bumetanide were tested as inhibitors of the zinc enzyme carbonic anhydrases (CAs, EC 4.2.1.1). These drugs were discovered in a period when only isoform CA II w...
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Veröffentlicht in: | Organic & biomolecular chemistry 2008-01, Vol.6 (14), p.2499-2506 |
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description | Sulfonamide diuretics such as hydrochlorothiazide, hydroflumethiazide, quinethazone, metolazone, chlorthalidone, indapamide, furosemide and bumetanide were tested as inhibitors of the zinc enzyme carbonic anhydrases (CAs, EC 4.2.1.1). These drugs were discovered in a period when only isoform CA II was known and considered physiologically/pharmacologically relevant. We prove here that although acting as moderate to weak inhibitors of CA II, all these drugs considerably inhibit other isozymes known nowadays to be involved in critical physiologic processes, among the 16 CAs present in vertebrates. Some low nanomolar/subnanomolar inhibitors against such isoforms were detected, such as among others metolazone against CA VII, XII and XIII, chlorthalidone against CA VB, VII, IX, XII and XIII, indapamide against CA VII, IX, XII and XIII, furosemide against CA I, II and XIV, and bumethanide against CA IX and XII. The X-ray crystal structure of the CA II-indapamide adduct was also resolved at high resolution, and the binding of this sulfonamide to the enzyme was compared to that of dichlorophenamide, sulpiride and a pyridinium containing sulfonamide. Indapamide binds to CA II in a manner not seen earlier for any other CA inhibitor, which might be important for the design of compounds with a different inhibition profile. |
doi_str_mv | 10.1039/b800767e |
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Sulfonamide diuretics revisited--old leads for new applications?</title><source>MEDLINE</source><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Temperini, Claudia ; Cecchi, Alessandro ; Scozzafava, Andrea ; Supuran, Claudiu T</creator><creatorcontrib>Temperini, Claudia ; Cecchi, Alessandro ; Scozzafava, Andrea ; Supuran, Claudiu T</creatorcontrib><description>Sulfonamide diuretics such as hydrochlorothiazide, hydroflumethiazide, quinethazone, metolazone, chlorthalidone, indapamide, furosemide and bumetanide were tested as inhibitors of the zinc enzyme carbonic anhydrases (CAs, EC 4.2.1.1). These drugs were discovered in a period when only isoform CA II was known and considered physiologically/pharmacologically relevant. We prove here that although acting as moderate to weak inhibitors of CA II, all these drugs considerably inhibit other isozymes known nowadays to be involved in critical physiologic processes, among the 16 CAs present in vertebrates. Some low nanomolar/subnanomolar inhibitors against such isoforms were detected, such as among others metolazone against CA VII, XII and XIII, chlorthalidone against CA VB, VII, IX, XII and XIII, indapamide against CA VII, IX, XII and XIII, furosemide against CA I, II and XIV, and bumethanide against CA IX and XII. The X-ray crystal structure of the CA II-indapamide adduct was also resolved at high resolution, and the binding of this sulfonamide to the enzyme was compared to that of dichlorophenamide, sulpiride and a pyridinium containing sulfonamide. Indapamide binds to CA II in a manner not seen earlier for any other CA inhibitor, which might be important for the design of compounds with a different inhibition profile.</description><identifier>ISSN: 1477-0520</identifier><identifier>EISSN: 1477-0539</identifier><identifier>DOI: 10.1039/b800767e</identifier><identifier>PMID: 18600270</identifier><language>eng</language><publisher>England</publisher><subject>Carbonic Anhydrase II - antagonists & inhibitors ; Carbonic Anhydrase II - chemistry ; Carbonic Anhydrase II - metabolism ; Carbonic Anhydrase Inhibitors - metabolism ; Carbonic Anhydrase Inhibitors - pharmacology ; Carbonic Anhydrases - chemistry ; Carbonic Anhydrases - metabolism ; Catalysis ; Crystallography, X-Ray ; Diuretics - metabolism ; Diuretics - pharmacology ; Drug Design ; Drug Evaluation, Preclinical ; Humans ; Indapamide - chemistry ; Isoenzymes - antagonists & inhibitors ; Isoenzymes - chemistry ; Isoenzymes - metabolism ; Models, Molecular ; Protein Conformation ; Sulfonamides - metabolism ; Sulfonamides - pharmacology</subject><ispartof>Organic & biomolecular chemistry, 2008-01, Vol.6 (14), p.2499-2506</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c306t-266f18638a48cd89d57c5869a42d1328f1166e746449d73c22c4060376d5f9603</citedby><cites>FETCH-LOGICAL-c306t-266f18638a48cd89d57c5869a42d1328f1166e746449d73c22c4060376d5f9603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18600270$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Temperini, Claudia</creatorcontrib><creatorcontrib>Cecchi, Alessandro</creatorcontrib><creatorcontrib>Scozzafava, Andrea</creatorcontrib><creatorcontrib>Supuran, Claudiu T</creatorcontrib><title>Carbonic anhydrase inhibitors. Sulfonamide diuretics revisited--old leads for new applications?</title><title>Organic & biomolecular chemistry</title><addtitle>Org Biomol Chem</addtitle><description>Sulfonamide diuretics such as hydrochlorothiazide, hydroflumethiazide, quinethazone, metolazone, chlorthalidone, indapamide, furosemide and bumetanide were tested as inhibitors of the zinc enzyme carbonic anhydrases (CAs, EC 4.2.1.1). These drugs were discovered in a period when only isoform CA II was known and considered physiologically/pharmacologically relevant. We prove here that although acting as moderate to weak inhibitors of CA II, all these drugs considerably inhibit other isozymes known nowadays to be involved in critical physiologic processes, among the 16 CAs present in vertebrates. Some low nanomolar/subnanomolar inhibitors against such isoforms were detected, such as among others metolazone against CA VII, XII and XIII, chlorthalidone against CA VB, VII, IX, XII and XIII, indapamide against CA VII, IX, XII and XIII, furosemide against CA I, II and XIV, and bumethanide against CA IX and XII. The X-ray crystal structure of the CA II-indapamide adduct was also resolved at high resolution, and the binding of this sulfonamide to the enzyme was compared to that of dichlorophenamide, sulpiride and a pyridinium containing sulfonamide. Indapamide binds to CA II in a manner not seen earlier for any other CA inhibitor, which might be important for the design of compounds with a different inhibition profile.</description><subject>Carbonic Anhydrase II - antagonists & inhibitors</subject><subject>Carbonic Anhydrase II - chemistry</subject><subject>Carbonic Anhydrase II - metabolism</subject><subject>Carbonic Anhydrase Inhibitors - metabolism</subject><subject>Carbonic Anhydrase Inhibitors - pharmacology</subject><subject>Carbonic Anhydrases - chemistry</subject><subject>Carbonic Anhydrases - metabolism</subject><subject>Catalysis</subject><subject>Crystallography, X-Ray</subject><subject>Diuretics - metabolism</subject><subject>Diuretics - pharmacology</subject><subject>Drug Design</subject><subject>Drug Evaluation, Preclinical</subject><subject>Humans</subject><subject>Indapamide - chemistry</subject><subject>Isoenzymes - antagonists & inhibitors</subject><subject>Isoenzymes - chemistry</subject><subject>Isoenzymes - metabolism</subject><subject>Models, Molecular</subject><subject>Protein Conformation</subject><subject>Sulfonamides - metabolism</subject><subject>Sulfonamides - pharmacology</subject><issn>1477-0520</issn><issn>1477-0539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEtLxDAYRYMozjgK_gLJStx0_PJo0qxEBl8w4EJdlzRJmUjb1KRV5t9bmVFX9y4Ol8tB6JzAkgBT11UBIIV0B2hOuJQZ5Ewd_nUKM3SS0jsAUVLwYzQjhQCgEuaoXOlYhc4brLvN1kadHPbdxld-CDEt8cvY1KHTrbcOWz9GN3iTcHSfPvnB2SwLjcWN0zbhOkTcuS-s-77xRg8-dOnmFB3VuknubJ8L9HZ_97p6zNbPD0-r23VmGIgho0LU0ylWaF4YWyibS5MXQmlOLWG0qAkRwkkuOFdWMkOp4SCASWHzWk1lgS53u30MH6NLQ9n6ZFzT6M6FMZVCUUVBiAm82oEmhpSiq8s--lbHbUmg_JFZ_sqc0Iv95li1zv6De3vsG1fRbnQ</recordid><startdate>20080101</startdate><enddate>20080101</enddate><creator>Temperini, Claudia</creator><creator>Cecchi, Alessandro</creator><creator>Scozzafava, Andrea</creator><creator>Supuran, Claudiu T</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20080101</creationdate><title>Carbonic anhydrase inhibitors. Sulfonamide diuretics revisited--old leads for new applications?</title><author>Temperini, Claudia ; Cecchi, Alessandro ; Scozzafava, Andrea ; Supuran, Claudiu T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c306t-266f18638a48cd89d57c5869a42d1328f1166e746449d73c22c4060376d5f9603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Carbonic Anhydrase II - antagonists & inhibitors</topic><topic>Carbonic Anhydrase II - chemistry</topic><topic>Carbonic Anhydrase II - metabolism</topic><topic>Carbonic Anhydrase Inhibitors - metabolism</topic><topic>Carbonic Anhydrase Inhibitors - pharmacology</topic><topic>Carbonic Anhydrases - chemistry</topic><topic>Carbonic Anhydrases - metabolism</topic><topic>Catalysis</topic><topic>Crystallography, X-Ray</topic><topic>Diuretics - metabolism</topic><topic>Diuretics - pharmacology</topic><topic>Drug Design</topic><topic>Drug Evaluation, Preclinical</topic><topic>Humans</topic><topic>Indapamide - chemistry</topic><topic>Isoenzymes - antagonists & inhibitors</topic><topic>Isoenzymes - chemistry</topic><topic>Isoenzymes - metabolism</topic><topic>Models, Molecular</topic><topic>Protein Conformation</topic><topic>Sulfonamides - metabolism</topic><topic>Sulfonamides - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Temperini, Claudia</creatorcontrib><creatorcontrib>Cecchi, Alessandro</creatorcontrib><creatorcontrib>Scozzafava, Andrea</creatorcontrib><creatorcontrib>Supuran, Claudiu T</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Organic & biomolecular chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Temperini, Claudia</au><au>Cecchi, Alessandro</au><au>Scozzafava, Andrea</au><au>Supuran, Claudiu T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Carbonic anhydrase inhibitors. Sulfonamide diuretics revisited--old leads for new applications?</atitle><jtitle>Organic & biomolecular chemistry</jtitle><addtitle>Org Biomol Chem</addtitle><date>2008-01-01</date><risdate>2008</risdate><volume>6</volume><issue>14</issue><spage>2499</spage><epage>2506</epage><pages>2499-2506</pages><issn>1477-0520</issn><eissn>1477-0539</eissn><abstract>Sulfonamide diuretics such as hydrochlorothiazide, hydroflumethiazide, quinethazone, metolazone, chlorthalidone, indapamide, furosemide and bumetanide were tested as inhibitors of the zinc enzyme carbonic anhydrases (CAs, EC 4.2.1.1). These drugs were discovered in a period when only isoform CA II was known and considered physiologically/pharmacologically relevant. We prove here that although acting as moderate to weak inhibitors of CA II, all these drugs considerably inhibit other isozymes known nowadays to be involved in critical physiologic processes, among the 16 CAs present in vertebrates. Some low nanomolar/subnanomolar inhibitors against such isoforms were detected, such as among others metolazone against CA VII, XII and XIII, chlorthalidone against CA VB, VII, IX, XII and XIII, indapamide against CA VII, IX, XII and XIII, furosemide against CA I, II and XIV, and bumethanide against CA IX and XII. The X-ray crystal structure of the CA II-indapamide adduct was also resolved at high resolution, and the binding of this sulfonamide to the enzyme was compared to that of dichlorophenamide, sulpiride and a pyridinium containing sulfonamide. Indapamide binds to CA II in a manner not seen earlier for any other CA inhibitor, which might be important for the design of compounds with a different inhibition profile.</abstract><cop>England</cop><pmid>18600270</pmid><doi>10.1039/b800767e</doi><tpages>8</tpages></addata></record> |
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subjects | Carbonic Anhydrase II - antagonists & inhibitors Carbonic Anhydrase II - chemistry Carbonic Anhydrase II - metabolism Carbonic Anhydrase Inhibitors - metabolism Carbonic Anhydrase Inhibitors - pharmacology Carbonic Anhydrases - chemistry Carbonic Anhydrases - metabolism Catalysis Crystallography, X-Ray Diuretics - metabolism Diuretics - pharmacology Drug Design Drug Evaluation, Preclinical Humans Indapamide - chemistry Isoenzymes - antagonists & inhibitors Isoenzymes - chemistry Isoenzymes - metabolism Models, Molecular Protein Conformation Sulfonamides - metabolism Sulfonamides - pharmacology |
title | Carbonic anhydrase inhibitors. Sulfonamide diuretics revisited--old leads for new applications? |
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