93439-36-2Relevant academic research and scientific papers
Synthesis and evaluation of 2,4,5-trisubstitutedthiazoles as carbonic anhydrase-III inhibitors
Al-Jaidi, Bilal A.,Al-dhoun, Mohammad A.,Bardaweel, Sanaa K.,Bataineh, Yazan A.,Dakkah, Abdel Naser,Deb, Pran Kishore,Khames Aga, Qutaiba Ahmed Al,Mailavaram, Raghuprasad,Nair, Anroop B.,Telfah, Soha Taher,Venugopala, Katharigatta N.,Ahmad Al-Subeihi, Ala’ Ali,Odetallah, Haifa’a Marouf
, p. 1483 - 1490 (2020)
A series of 17 compounds (12–16 b) with 2,4,5-trisubstitutedthiazole scaffold having 5-aryl group, 4-carboxylic acid/ester moiety, and 2-amino/amido/ureido functional groups were synthesised, characterised, and evaluated for their carbonic anhydrase (CA)-III inhibitory activities using the size exclusion Hummel–Dreyer method (HDM) of chromatography. Compound 12a with a free amino group at the 2-position, carboxylic acid moiety at the 4-position, and a phenyl ring at the 5-position of the scaffold was found to be the most potent CA-III inhibitor (Ki = 0.5 μM). The presence of a carboxylic acid group at the 4-position of the scaffold was found to be crucial for the CA-III inhibitory activity. Furthermore, replacement of the free amino group with an amide and urea group resulted in a significant reduction of activity (compounds 13c and 14c, Ki = 174.1 and 186.2 μM, respectively). Thus, compound 12a (2-amino-5-phenylthiazole-4-carboxylic acid) can be considered as the lead molecule for further modification and development of more potent CA-III inhibitors.
