Abstract |
We report a panel of carboxylates and sulfonamides incorporating phthalic anhydride and phthalimide moieties in their structure and their interaction with the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1). They were synthesized from substituted anthranilic acids and trimellitic anhydride chloride, followed by reaction with primary amines and were tested for the inhibition of five physiologically relevant CA isoforms, the human (h) hCA I, II, IV, VII and XII, some of which are involved in serious pathologies (CA II, IV and XII in glaucoma; CA VII in epilepsy; CA XII in some solid tumors). The carboxylic acids were generally poor inhibitors of isoforms hCA I, II and IV but were highly effective, low nanomolar inhibitors of hCA VII and XII. The sulfonamides inhibited all isoforms significantly, and some of them were sub-nanomolar hCA VII inhibitors, although their isoform selectivity was lower compared to the carboxylates. This study proves that carboxylic acids incorporating a phthalic anhydride/ phthalimide based scaffold may lead to isoform-selective inhibitors by applying the tail approach, mostly used up until now for obtaining sulfonamide, sulfamide and sulfamate CA inhibitors.
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Authors | Adel S El-Azab, Alaa A-M Abdel-Aziz, Rezk R Ayyad, Mariangela Ceruso, Claudiu T Supuran |
Journal | Bioorganic & medicinal chemistry
(Bioorg Med Chem)
Vol. 24
Issue 1
Pg. 20-5
(Jan 01 2016)
ISSN: 1464-3391 [Electronic] England |
PMID | 26678172
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2015 Elsevier Ltd. All rights reserved. |
Chemical References |
- Carbonic Anhydrase Inhibitors
- Isoenzymes
- Phthalic Anhydrides
- Phthalimides
- Sulfonamides
- ortho-Aminobenzoates
- Acetazolamide
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Topics |
- Acetazolamide
(chemistry)
- Carbonic Anhydrase Inhibitors
(chemical synthesis, chemistry)
- Humans
- Isoenzymes
(antagonists & inhibitors)
- Phthalic Anhydrides
(chemical synthesis, chemistry)
- Phthalimides
(chemical synthesis, chemistry)
- Sulfonamides
(chemical synthesis, chemistry)
- ortho-Aminobenzoates
(chemical synthesis, chemistry)
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