Stereochemistry matters: Inhibition of carbonic anhydrase II by amino acid derived sulfamates depends on their absolute configuration-Reference-Cited by-同舟云学术

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Stereochemistry matters: Inhibition of carbonic anhydrase II by amino acid derived sulfamates depends on their absolute configuration

Published:2024-08 Issue: Volume:11 Page:100162
ISSN:2772-4174
Container-title:European Journal of Medicinal Chemistry Reports
language:en
Short-container-title:European Journal of Medicinal Chemistry Reports

Author:

Denner Toni C.^ORCID,Klett Elsa L.,Heise Niels V.^ORCID,Csuk René^ORCID

Publisher

Elsevier BV

Reference31 articles.

1. Carbonic anhydrase II activators in osteopetrosis treatment: a review;Alkhayal;Curr. Issues Mol. Biol.,2023

2. Response to perspectives on the classical enzyme carbonic anhydrase and the search for inhibitors;Angeli;Biophys. J.,2021

3. Targeting carbonic anhydrase isozymes in the treatment of neurological disorders;Aspatwar;Prog. Drug Res.,2021

4. Carbonic anhydrase inhibitors and epilepsy: state of the art and future perspectives;Ciccone;Molecules,2021

5. Carbonic anhydrase, its inhibitors and vascular function;García-Llorca;Front. Mol. Biosci.,2024

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Arylsulfonamido-alkyl-sulfamates act as inhibitors of bovine carbonic anhydrase II;European Journal of Medicinal Chemistry Reports;2024-12

2. Synthesis and Enzymatic Evaluation of a Small Library of Substituted Phenylsulfonamido-Alkyl Sulfamates towards Carbonic Anhydrase II;Molecules;2024-06-25

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