Nimesulide linked acyl thioureas potent carbonic anhydrase I, II and α-glucosidase inhibitors: Design, synthesis and molecular docking studies
Ahmed, Atteeque, Sha, Imran, Saeed, Aamer, Shabir, Ghulam, Saleem, Arslan, Taslimi, Parham, Tok, Tugba Taskin, Kirici, Mahinur, Uc, Eda Mehtap, Hashmi, Muhammad Zaffar
Molecular hybridization has emerged as an interesting strategy to improve the effectiveness and the scope of well-known drugs. Nimesulide has been used as non-steroidal anti-inflammatory (NSAID) drug for decades and marketed as NIMS (TM). Nimesulide (3) possesses a nitro group which shows toxic behavior. To enhance the scope and efficacy of the drug nitro group was reduced to amino group (4) and reacted with isothiocyanates of different substituted acid chlorides to afford Nimesulide-acyl thiourea conjugates (5a-n). In the present research work 14 derivatives were synthesized and tested for carbonic anhydrase I, II and alpha-glucosidase Inhibition assay. These findings established that all new derivatives are more effective alpha-amylase inhibitors than Acarbose (IC50: 10000 nM) used as a positive control alpha-amylase inhibitor. Among the tested compounds 5g, 5l and 5m were determined to be the best hCA I, II inhibitors.
- Journal
- EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY REPORTS
- Year
- 2022
- Volume
- 6
- ISSN
- 2772-4174
- DOI
- 10.1016/j.ejmcr.2022.100082
- WoS UID
- WOS:001097149200005