Structural Determinants of the Selectivity of 3‐Benzyluracil‐1‐acetic Acids toward Human Enzymes Aldose Reductase and AKR1B10. Issue 12 (9th November 2015)

• Record Type: Journal Article
• Authors: Ruiz, Francesc X.; Cousido‐Siah, Alexandra; Porté, Sergio; Domínguez, Marta; Crespo, Isidro; Rechlin, Chris; Mitschler, André; de Lera, Ángel R.; Martín, María Jesús; de la Fuente, Jesús Ángel; Klebe, Gerhard; Parés, Xavier; Farrés, Jaume; Podjarny, Alberto
• Is Part Of: ChemMedChem. Volume 10:Issue 12(2015:Dec.)
• Page Start: 1989
• Page End: 2003
• Publication Date: 2015-11-09
• Subjects: aldose reductase -- AKR1B10 -- drug design -- steric hindrance -- buried water molecule; Pharmaceutical chemistry -- Periodicals; 615.19005
• DOI: 10.1002/cmdc.201500393
• Languages: English
• ISSNs: 1860-7179

Abstract

Abstract: The human enzymes aldose reductase (AR) and AKR1B10 have been thoroughly explored in terms of their roles in diabetes, inflammatory disorders, and cancer. In this study we identified two new lead compounds, 2‐(3‐(4‐chloro‐3‐nitrobenzyl)‐2, 4‐dioxo‐3, 4‐dihydropyrimidin‐1(2 H )‐yl)acetic acid (JF0048, 3 ) and 2‐(2, 4‐dioxo‐3‐(2, 3, 4, 5‐tetrabromo‐6‐methoxybenzyl)‐3, 4‐dihydropyrimidin‐1(2 H )‐yl)acetic acid (JF0049, 4 ), which selectively target these enzymes. Although3 and4 share the 3‐benzyluracil‐1‐acetic acid scaffold, they have different substituents in their aryl moieties. Inhibition studies along with thermodynamic and structural characterizations of both enzymes revealed that the chloronitrobenzyl moiety of compound3 can open the AR specificity pocket but not that of the AKR1B10 cognate. In contrast, the larger atoms at the ortho and/or meta positions of compound4 prevent the AR specificity pocket from opening due to steric hindrance and provide a tighter fit to the AKR1B10 inhibitor binding pocket, probably enhanced by the displacement of a disordered water molecule trapped in a hydrophobic subpocket, creating an enthalpic signature. Furthermore, this selectivity also occurs in the cell, which enables the development of a more efficient drug design strategy: compound3 prevents sorbitol accumulation in human retinal ARPE‐19 cells, whereas4 stops proliferation in human lung cancer NCI‐H460 cells. Abstract : Selective targeting : We identified two new lead compounds that selectively target the human enzymes aldose reductase and AKR1B10, which are involved in diabetes, cancer, and inflammation. Inhibition studies along with thermodynamic and structural characterization led to the identification of determinants for this selectivity, unveiling new possibilities for structure‐based drug design.