An N,N-bis(p-methoxybenzyl)-protected a-acetyl-a-diazo- methane sulfonamide proved to be a useful building block for accessing new 5-methyl-1,2,3-thiadiazole-4-sulfonamide as well as methyl 3-sulfamoyl-1H-pyrazole-5-carboxylate. The latter was further subjected to N-alkylation and N-arylation reactions. All resulting compounds showed potent inhibition of I, II and particularly of cancer-related IX and XII isoforms of human carbonic anhydrase.

A new way of synthesizing heterocyclic primary sulfonamide probes for carbonic anhydrase / Krivovicheva, Vasilisa; Bubyrev, Andrey; Kalinin, Stanislav; Dar'in, Dmitry; Gureev, Maxim; Vullo, Daniela; Krasavin, Mikhail; Korsakov, Mikhail; Supuran, Claudiu T.. - In: MENDELEEV COMMUNICATIONS. - ISSN 0959-9436. - ELETTRONICO. - 33:(2023), pp. 0-0. [10.1016/j.mencom.2023.04.009]

A new way of synthesizing heterocyclic primary sulfonamide probes for carbonic anhydrase

Vullo, Daniela;Supuran, Claudiu T.
2023

Abstract

An N,N-bis(p-methoxybenzyl)-protected a-acetyl-a-diazo- methane sulfonamide proved to be a useful building block for accessing new 5-methyl-1,2,3-thiadiazole-4-sulfonamide as well as methyl 3-sulfamoyl-1H-pyrazole-5-carboxylate. The latter was further subjected to N-alkylation and N-arylation reactions. All resulting compounds showed potent inhibition of I, II and particularly of cancer-related IX and XII isoforms of human carbonic anhydrase.
2023
33
0
0
Krivovicheva, Vasilisa; Bubyrev, Andrey; Kalinin, Stanislav; Dar'in, Dmitry; Gureev, Maxim; Vullo, Daniela; Krasavin, Mikhail; Korsakov, Mikhail; Supuran, Claudiu T.
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1311447
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