2021
De-la-Cruz-Martínez, L.; Duran-Becerra, C.; González-Andrade, M.; Páez-Franco, J.C.; Germán-Acacio, J.M.; Espinosa-Chávez, J.; Torres-Valencia, J.M.; Pérez-Villanueva, J.; Palacios-Espinosa, J.F.; Soria-Arteche, O.; Cortés-Benítez, F. Indole- and Pyrazole-Glycyrrhetinic Acid Derivatives as PTP1B Inhibitors: Synthesis, In Vitro and In Silico Studies. Molecules 2021, 26, 4375. https://doi.org/10.3390/molecules26144375
Abstract
Regulating insulin and leptin levels using a protein tyrosine phosphatase 1B (PTP1B) inhibitor is an attractive strategy to treat diabetes and obesity. Glycyrrhetinic acid (GA), a triterpenoid, may weakly inhibit this enzyme. Nonetheless, semisynthetic derivatives of GA have not been developed as PTP1B inhibitors to date. Herein we describe the synthesis and evaluation of two series of indole- and N-phenylpyrazole-GA derivatives (4a?f and 5a?f). We measured their inhibitory activity and enzyme kinetics against PTP1B using p-nitrophenylphosphate (pNPP) assay. GA derivatives bearing substituted indoles or N-phenylpyrazoles fused to their A-ring showed a 50% inhibitory concentration for PTP1B in a range from 2.5 to 10.1 M. The trifluoromethyl derivative of indole-GA (4f) exhibited non-competitive inhibition of PTP1B as well as higher potency (IC50 = 2.5 M) than that of positive controls ursolic acid (IC50 = 5.6 M), claramine (IC50 = 13.7 M) and suramin (IC50 = 4.1 M). Finally, docking and molecular dynamics simulations provided the theoretical basis for the favorable activity of the designed compounds.
Lead, Cadmium and Cobalt (Pb, Cd, and Co) Leaching of Glass-Clay Containers by pH Effect of Food
Antioxidant constituents from Geranium bellum Rose
Effect of the particle size on the activity of MoOxCy catalysts for the isomerization of heptane
Estudio químico de cinco plantas mexicanas de uso común en la medicina tradicional