Aryl derivatives of 3H-1,2-benzoxathiepine 2,2-dioxide as carbonic anhydrase inhibitors

A new series of homosulfocoumarins (3H-1,2-benzoxathiepine 2,2-dioxides) possessing various substitution patterns and moieties in the 7, 8 or 9 position of the heterocylic ring were prepared by original procedures and investigated for the inhibition of four physiologically relevant carbonic anhydras...

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Vydáno v:J Enzyme Inhib Med Chem
Hlavní autoři: Pustenko, Aleksandrs, Nocentini, Alessio, Balašova, Anastasija, Alafeefy, Ahmed, Krasavin, Mikhail, Žalubovskis, Raivis, Supuran, Claudiu T.
Médium: Artigo
Jazyk:Inglês
Vydáno: Taylor & Francis 2019
Témata:
Research Paper
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6896485/
https://ncbi.nlm.nih.gov/pubmed/31790605
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/14756366.2019.1695795
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