[1] CHEN X,YANG Y C,MA B,et al. Design and synthesis of potent and selective aldose reductase inhibitors based on pyridylthiadiazine scaffold[J]. European Journal of Medicinal Chemistry,2011,46(5):1536-1544. [2] DA SETTIMO F,PRIMOFIORE G,DA SETTIMO A,et al. Novel, highly potent aldose reductase inhibitors:cyano (2-oxo-2,3-dihydroindol-3-yl) acetic acid derivatives[J]. J. Med. Chem.,2003, 46(8):1419-1428. [3] DA SETTIMO F,PRIMOFIORE G,LA MOTTA C, et al. Naphtho[1,2-d]isothiazole acetic acid derivatives as a novel class of selective aldose reductase inhibitors[J]. J. Med. Chem.,2005,48(22):6897-6907. [4] EL-KABBANI O,CARBONE V,DARMANIN C,et al. Structure of aldehyde reductase holoenzyme in complex with the potent aldose reductase inhibitor fidarestat:implications for inhibitor binding and selectivity[J]. J. Med. Chem.,2005,48(17):5536-5542. [5] LA MOTTA C,SARTINI S,MUGNAINI L,et al. Pyrido[1,2-a] pyrimidin-4-one derivatives as a novel class of selective aldose reductase inhibitors exhibiting antioxidant activity[J]. J. Med. Chem., 2007,50(20):4917-4927. [6] ROBERTI M,PIZZIRANI D,SIMONI D,et al. Synthesis and biological evaluation of resveratrol and analogues as apoptosisinducing agents[J]. J. Med. Chem.,2003,46(16):3546-3554. [7] VAN ZANDT M C,JONES M L,GUNN D E,et al. Discovery of 3-[(4,5,7-trifluorobenzothiazol-2-yl)methyl]indole-N-acetic acid (Lidorestat) and congeners as highly potent and selective inhibitors of aldose reductase for treatment of chronic diabetic complications[J]. J. Med. Chem.,2005,48(9):3141-3152. [8] CHEN X,ZHANG S,YANG Y C,et al. 1,2-Benzothiazine 1,1-dioxide carboxylate derivatives as novel potent inhibitors of aldose reductase[J]. Bioorganic & Medicinal Chemistry,2011,19(23):7262-7269. [9] CHEN X,ZHU C J,GUO F,et al. Acetic acid derivatives of 3,4-dihydro-2h-1,2,4-benzothiadiazine 1,1-dioxide as a novel class of potent aldose reductase inhibitors[J]. Journal of Medicinal Chemistry,2010,53(23):330-344. [10] YANG Y C,ZHANG S Z,WU B B,et al. An efficient synthesis of quinoxalinone derivatives as potent inhibitors of aldose reductase[J]. Chem. Med. Chem.,2012,7:823-835. [11] ZHANG S Z,CHEN X,PARVEEN S,et al. Synthesis and in vitro pharmacological studies of C(7) modification of 3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide as aldose reductase inhibitor[J]. Chem. Med. Chem.,2013,8,603-613. [12] 曾维才,石碧. 天然产物抗氧化活性的常见评价方法[J]. 化工进展,2013,32(6):1205-1213. |