期刊
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY
卷 35, 期 1, 页码 549-554出版社
TAYLOR & FRANCIS LTD
DOI: 10.1080/14756366.2020.1715388
关键词
Carbonic anhydrase; inhibitor; isoform XII; isoform-selective inhibitor; carboxylate
资金
- King Saud University, Riyadh, Saudi Arabia [RSP-2019/50]
A small series of 2,4-dioxothiazolidinyl acetic acids was prepared from thiourea, chloroacetic acid, aromatic aldehydes, and ethyl-2-bromoacetate. They were assayed for the inhibition of four physiologically relevant carbonic anhydrase (CA, EC 4.2.1.1) isoforms of human (h) origin, the cytosolic hCA I and II, and the transmembrane hCA IX and XII, involved among others in tumorigenesis (hCA IX and XII) and glaucoma (hCA II and XII). The two cytosolic isoforms were not inhibited by these carboxylates, which were also rather ineffective as hCA IX inhibitors. On the other hand, they showed submicromolar hCA XII inhibition, with K(I)s in the range of 0.30-0.93 mu M, making them highly CA XII-selective inhibitors.
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