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Campo DC | Valor | Lengua/Idioma |
---|---|---|
dc.creator | Riafrecha, Leonardo Ezequiel | - |
dc.creator | Bua, Silvia | - |
dc.creator | Supuran, Claudiu T. | - |
dc.creator | Colinas, Pedro Alfonso | - |
dc.date | 2018-08-08T18:37:53Z | - |
dc.date | 2018-08-08T18:37:53Z | - |
dc.date | 2016-07 | - |
dc.date | 2018-08-08T15:02:01Z | - |
dc.date.accessioned | 2019-04-29T15:26:12Z | - |
dc.date.available | 2019-04-29T15:26:12Z | - |
dc.date.issued | 2016-07 | - |
dc.identifier | Riafrecha, Leonardo Ezequiel; Bua, Silvia; Supuran, Claudiu T.; Colinas, Pedro Alfonso; Synthesis and carbonic anhydrase inhibitory effects of new N-glycosylsulfonamides incorporating the phenol moiety; Pergamon-Elsevier Science Ltd; Biorganic and Medicinal Chemistry Letters; 26; 16; 7-2016; 3892-3895 | - |
dc.identifier | 0960-894X | - |
dc.identifier | http://hdl.handle.net/11336/54631 | - |
dc.identifier | CONICET Digital | - |
dc.identifier | CONICET | - |
dc.identifier.uri | http://rodna.bn.gov.ar:8080/jspui/handle/bnmm/294155 | - |
dc.description | A small series of N-glycosylsulfonamides incorporating the phenol moiety has been prepared by Ferrier sulfonamidoglycosylation of D-glycals. N-Glycosides were tested for the inhibition of four isoforms of carbonic anhydrase. In this study, all compounds showed good inhibitory activity against hCA I and II, with selectivity against the cytosolic hCA II versus the tumor associated isozymes. These results confirm that attaching carbohydrate moieties to CA phenol pharmacophore improves and enhances its inhibitory activity. | - |
dc.description | Fil: Riafrecha, Leonardo Ezequiel. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Departamento de Química. Laboratorio de Estudio de Compuestos Orgánicos; Argentina | - |
dc.description | Fil: Bua, Silvia. Università degli Studi di Firenze; Italia | - |
dc.description | Fil: Supuran, Claudiu T.. Università degli Studi di Firenze; Italia | - |
dc.description | Fil: Colinas, Pedro Alfonso. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Departamento de Química. Laboratorio de Estudio de Compuestos Orgánicos; Argentina | - |
dc.format | application/pdf | - |
dc.format | application/pdf | - |
dc.format | application/pdf | - |
dc.language | eng | - |
dc.publisher | Pergamon-Elsevier Science Ltd | - |
dc.relation | info:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.1016/j.bmcl.2016.07.015 | - |
dc.relation | info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0960894X1630717X | - |
dc.rights | info:eu-repo/semantics/restrictedAccess | - |
dc.rights | https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ | - |
dc.source | reponame:CONICET Digital (CONICET) | - |
dc.source | instname:Consejo Nacional de Investigaciones Científicas y Técnicas | - |
dc.source | instacron:CONICET | - |
dc.subject | CARBONIC ANHYRASES | - |
dc.subject | GLYCOMIMETIC | - |
dc.subject | SULFONAMIDOGLYCOSYLATION | - |
dc.subject | Otras Ciencias Químicas | - |
dc.subject | Ciencias Químicas | - |
dc.subject | CIENCIAS NATURALES Y EXACTAS | - |
dc.title | Synthesis and carbonic anhydrase inhibitory effects of new N-glycosylsulfonamides incorporating the phenol moiety | - |
dc.type | info:eu-repo/semantics/article | - |
dc.type | info:eu-repo/semantics/publishedVersion | - |
dc.type | info:ar-repo/semantics/articulo | - |
Aparece en las colecciones: | CONICET |
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