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- W4368361670 abstract "Aim: Among 15 human (h) carbonic anhydrase (CA; EC 4.2.1.1) isoforms, two (hCA IX and XII) play important roles in the growth and survival of tumor cells, making them therapeutic targets for cancer treatment. This study aimed to develop novel sulfonamide-based compounds as selective hCA IX and XII inhibitors. Materials & methods: A library of novel N-sulfonyl carbamimidothioates was obtained for CA inhibitory activity studies against four hCA isoforms. Results: None of the developed compounds displayed inhibitory potential against off-target isoforms hCA I and II. However, they effectively inhibited tumor-associated hCA IX and XII. Conclusion: The present study suggests potent lead compounds as selective hCA IX and XII inhibitors with anticancer activity." @default.
- W4368361670 created "2023-05-05" @default.
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- W4368361670 date "2023-04-01" @default.
- W4368361670 modified "2023-10-05" @default.
- W4368361670 title "Investigation of carbonic anhydrase inhibitory potency of (<i>Z/E</i>)-alkyl <i>N</i>‘-benzyl-<i>N</i>-(arylsulfonyl)-carbamimidothioates" @default.
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- W4368361670 doi "https://doi.org/10.4155/fmc-2022-0287" @default.
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