N-(Aroyl)-N-(arylmethyloxy)-α-alanines: Selective inhibitors of aldose reductase

被引:15
作者
Nencetti, Susanna [1 ]
La Motta, Concettina [1 ]
Rossello, Armando [1 ]
Sartini, Stefania [1 ]
Nuti, Elisa [1 ]
Ciccone, Lidia [2 ]
Orlandini, Elisabetta [1 ,3 ]
机构
[1] Univ Pisa, Dipartimento Farm, Via Bonanno 6, I-56126 Pisa, Italy
[2] CEA, iBiTec S, Serv Ingn Mol Prot SIMOPRO, F-91191 Gif Sur Yvette, France
[3] Univ Pisa, Dipartimento Sci Terra, Via S Maria 53, I-56126 Pisa, Italy
关键词
Diabetes mellitus; Aldose reductase (ALR2); Aldose reductase selective inhibitors; alpha-Alanines; DIABETIC COMPLICATIONS; SUPERFAMILY; DERIVATIVES; NEUROPATHY; ALDEHYDE; TARGET; ENZYME;
D O I
10.1016/j.bmc.2017.03.056
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aldose reductase (ALR2), a NADPH-dependent reductase, is the first and rate-limiting enzyme of the polyol pathway of glucose metabolism and is implicated in the pathogenesis of secondary diabetic complications. In the last decades, this enzyme has been targeted for inhibition but despite the numerous efforts made to identify potent and safe ALR2 inhibitors, many clinical candidates have been a failure. For this reason the research of new ALR2 inhibitors highly effective, selective and with suitable pharmacokinetic properties is still of great interest. In this paper some new N-(aroyl)-N-(arylmethyloxy)alanines have been synthesized and tested for their ability to inhibit ALR2. Some of the synthesized compounds exhibit IC50 in the low micromolar range and all have proved to be highly selective towards ALR2. The N-(aroyl)-N-(arylmethyloxy)-alpha-alanines are a promising starting point for the development of new ALR2 selective drugs with the aim of delaying the onset of diabetic complications. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3068 / 3076
页数:9
相关论文
共 33 条
[1]   Aldose Reductase Enzyme and its Implication to Major Health Problems of the 21st Century [J].
Alexiou, Polyxeni ;
Pegklidou, Kyriaki ;
Chatzopoulou, Maria ;
Nicolaou, Ioannis ;
Demopoulos, Vassilis J. .
CURRENT MEDICINAL CHEMISTRY, 2009, 16 (06) :734-752
[2]  
[Anonymous], GLOB REP DIAB
[3]   SYNTHESIS AND ALDOSE REDUCTASE INHIBITORY ACTIVITY OF N-(ARYLSULFONYL)GLYCINES AND N-(AROYL)-N-(ARYLMETHYLOXY)GLYCINES [J].
BALSAMO, A ;
BELFIORE, MS ;
MACCHIA, M ;
MARTINI, C ;
NENCETTI, S ;
ORLANDINI, E ;
ROSSELLO, A .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1994, 29 (10) :787-794
[4]   The atomic resolution structure of human aldose reductase reveals that rearrangement of a bound ligand allows the opening of the safety-belt loop [J].
Biadene, Marianna ;
Hazemann, Isabelle ;
Cousido, Alexandra ;
Ginell, Steve ;
Jochimiak, Andrzej ;
Sheldrick, George M. ;
Podjarny, Alberto ;
Schneider, Thomas R. .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 2007, 63 :665-672
[5]  
BOHREN KM, 1989, J BIOL CHEM, V264, P9547
[6]   Biochemistry and molecular cell biology of diabetic complications [J].
Brownlee, M .
NATURE, 2001, 414 (6865) :813-820
[7]   A SUPERFAMILY OF NADPH-DEPENDENT REDUCTASES IN EUKARYOTES AND PROKARYOTES [J].
CARPER, DA ;
WISTOW, G ;
NISHIMURA, C ;
GRAHAM, C ;
WATANABE, K ;
FUJII, Y ;
HAYASHI, H ;
HAYAISHI, O .
EXPERIMENTAL EYE RESEARCH, 1989, 49 (03) :377-388
[8]   Aldose reductase in diabetic microvascular complications [J].
Chung, SSM ;
Chung, SK .
CURRENT DRUG TARGETS, 2005, 6 (04) :475-486
[9]   Pursuing Aldose Reductase Inhibitors through in Situ Cross-Docking and Similarity-Based Virtual Screening [J].
Cosconati, Sandro ;
Marinelli, Luciana ;
La Motta, Concettina ;
Sartini, Stefania ;
Da Settimo, Federico ;
Olson, Arthur J. ;
Novellino, Ettore .
JOURNAL OF MEDICINAL CHEMISTRY, 2009, 52 (18) :5578-5581
[10]   Aldose reductase structures: implications for mechanism and inhibition [J].
El-Kabbani, O ;
Ruiz, F ;
Darmanin, C ;
Chung, RPT .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2004, 61 (7-8) :750-762