Department of Studies in Chemistry, University of Mysore, Manasagangotri, Mysore, India.
Arch Pharm (Weinheim). 2013 May;346(5):359-66. doi: 10.1002/ardp.201200470. Epub 2013 Apr 16.
A series of urea and thiourea derivatives of glutamic acid conjugated to 3-(1-piperazinyl)-1,2-benzisothiazole were synthesized, spectroscopically characterized, and evaluated for their in vitro antiglycation and urease inhibitory activities. Preliminary screening of the synthesized compounds 1-35 showed significant results. Amongst these, compounds 17-21 and 30-35 bearing fluoro and methoxy substituents, respectively, exhibited inhibitory potency greater than the reference standards. Hence, they may serve as new lead compounds for further development.
合成了一系列谷氨酸与 3-(1-哌嗪基)-1,2-苯并异噻唑相连的脲和硫脲衍生物,对其进行了光谱表征,并评价了它们的体外糖化抑制和脲酶抑制活性。对合成的化合物 1-35 进行了初步筛选,结果显示具有显著效果。其中,分别带有氟和甲氧基取代基的化合物 17-21 和 30-35 表现出比对照标准更强的抑制能力。因此,它们可能成为进一步开发的新先导化合物。