Design, synthesis and docking study of novel tetracyclic oxindole derivatives as α-glucosidase inhibitors. Issue 7 (1st April 2015)

• Record Type: Journal Article
• Authors: Han, Kailin; Li, Yashan; Zhang, Yazhou; Teng, Yuou; Ma, Ying; Wang, Meiyan; Wang, Runling; Xu, Weiren; Yao, Qingwei; Zhang, Yongmin; Qin, Haijuan; Sun, Hua; Yu, Peng
• Is Part Of: Bioorganic & medicinal chemistry letters. Volume 25:Issue 7(2015)
• Page Start: 1471
• Page End: 1475
• Publication Date: 2015-04-01
• Subjects: Tetracyclic isatins -- α-Glucosidase inhibitors -- Docking study -- Phenanthridine derivatives -- SAR study; Bioorganic chemistry -- Periodicals; Pharmaceutical chemistry -- Periodicals; 572
• DOI: 10.1016/j.bmcl.2015.02.031
• Languages: English
• ISSNs: 0960-894X

Abstract

Graphical abstract: Abstract: A series of novel tetracyclic oxindole derivatives were synthesized via tandem Suzuki coupling–Michael addition reaction catalyzed by palladium. Twenty derivatives were designed and synthesized in 6–8 steps in 8–20% overall yields. Their structures were confirmed by 1 H, 13 C NMR and LC/MS. These compounds were evaluated for α-glucosidase inhibitory activity in vitro. Compounds7c, 7d, 7e, 7g, 7h, and7i exhibited IC50 values of 32.3, 12.1, 15.7, 29.0, 16.0, and 4.8 μM, respectively, with potency all higher than that of the control standard acarbose (IC50 = 115.8 μM). Molecular docking studies revealed the existence of potential hydrogen bonding and hydrophobic interaction between the enzyme and the active compound7i .