Identification of new structure of indol-3-acetyl-arylsulfonohydrazide as potent α-glucosidase and α-amylase inhibitors and molecular docking

• Published in: JOURNAL OF MOLECULAR STRUCTURE
• Main Authors: Taha, Muhammad; Rahim, Fazal; Zaman, Khalid; Imran, Syahrul; Khan, Khalid Mohammed; Shah, Syed Adnan Ali; Uddin, Nizam
• Format: Article
• Language: English
• Published: ELSEVIER 2025
• Subjects: Chemistry
• Online Access: https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-recordWOS:001363793300001

Herein this work, indole analogs (1-16) were synthesized by treating 2-(1H-indol-3-yl)acetohydrazide with various aryl sulfonyl chloride in pyridine as solvent and screened for alpha-amylase and alpha-glucosidase inhibitory activity under positive control of standard drug acarbose (IC50 = 12.80 f 0.10 mu M /12.90 f 0.10 mu M. All analogs of the series appeared with excellent to good inhibitory activity as compared to standard drug. The inhibitory activity range for alpha-amylase is 0.70 f 0.01 mu M to 19.40 f 0.40 mu M, while for alpha-glucosidase inhibitory activity is 1.20 f 0.10 mu M to 20.40 f 0.40 mu M respectively. Most of the analogs appeared with excellent inhibitory activity, and some analogs like 5, 6, 7, 8, 9, 10,13 and 14 for both enzymes displayed many folds better inhibitory activity than standard drug acarbose. The influences of substituents on inhibitory activity were superficially resonated via structure activity relationship. Docking studies were established to confirm the binding interaction between analogs and active sites of enzymes.