Pharmacological Properties of Sulfonamide Derivatives, New Inhibitors of Carbonic Anhydrase

Selective blocking of individual isoforms of carbonic anhydrase (CA) is now one of the main directions in the development of its inhibitors. The new 1,2,4-oxadiazole-containing sulfonamides B12 and B13 predominantly block CA II and CA IX. The study of acute toxicity of B12 and B13 showed their safet...

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Vydáno v:Bulletin of experimental biology and medicine Ročník 175; číslo 2; s. 205 - 209
Hlavní autoři: Khokhlov, A. L., Shetnev, A. A., Korsakov, M. K., Fedorov, V. N., Tyushina, A. N., Volkhin, N. N., Vdovichenko, V. P.
Médium: Journal Article
Jazyk:angličtina
Vydáno: New York Springer US 01.06.2023
Springer
Springer Nature B.V
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ISSN:0007-4888, 1573-8221, 1573-8221
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Shrnutí:Selective blocking of individual isoforms of carbonic anhydrase (CA) is now one of the main directions in the development of its inhibitors. The new 1,2,4-oxadiazole-containing sulfonamides B12 and B13 predominantly block CA II and CA IX. The study of acute toxicity of B12 and B13 showed their safety. Substance B13 caused a relatively short-term, but rapid (within 30 min) decrease in the intraocular pressure in rabbits, which indicates the promise of its use for the emergency decrease in the intraocular pressure in medical practice. Analysis of the effects of sulfonamides on the functions of CNS showed that compound B12 probably exhibit tranquilizing activity; B13 is promising for the creation of drugs that have an antidepressant effect and at the same time increase the mental and physical performance.
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ISSN:0007-4888
1573-8221
1573-8221
DOI:10.1007/s10517-023-05835-w