Carbonic anhydrase inhibitors: Inhibition of human erythrocyte isozymes I and II with a series of phenolic acids.
Article Details
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Sarikaya SB, Gulcin I, Supuran CT
Carbonic anhydrase inhibitors: Inhibition of human erythrocyte isozymes I and II with a series of phenolic acids.
Chem Biol Drug Des. 2010 May;75(5):515-20. doi: 10.1111/j.1747-0285.2010.00965.x.
- PubMed ID
- 20486938 [ View in PubMed]
- Abstract
The inhibitory effects of some phenolic acids on the cytosolic human carbonic anhydrase (hCA, EC 4.2.1.1) isozymes hCA I and hCA II were investigated. Ellagic acid, gallic acid, ferulic acid, caffeic acid, quercetin, p-coumaric acid, p-hydroxybenzoic acid, and syringic acid showed K(I) values in the range of 99-1061 microm for hCA I and of 105-758 microm against hCA II, respectively. Quercetin (for hCA I), p-coumaric acid (for hCA II), and gallic acid (for hCA II) exhibited competitive inhibitory effects with 4-nitrophenyl acetate as substrate. All of the other phenolic acids were found as non-competitive inhibitors with 4-nitrophenylacetate as substrate for hCA I and hCA II. The phenolic acids investigated here showed thus interesting hCA I and hCA II inhibitory effects and might be used as leads for generating enzyme inhibitors possibly targeting other CA isoforms which have not been yet assayed for their interactions with such agents.
DrugBank Data that Cites this Article
- Binding Properties
Drug Target Property Measurement pH Temperature (°C) Acetazolamide Carbonic anhydrase 1 Ki (nM) 36000 7.4 25 Details Acetazolamide Carbonic anhydrase 2 Ki (nM) 3700 7.4 25 Details Ellagic acid Carbonic anhydrase 1 Ki (nM) 207000 7.4 25 Details Ellagic acid Carbonic anhydrase 2 Ki (nM) 146000 7.4 25 Details