dc.creator | Figueroa-Benavides C. | |
dc.creator | Matos M.J. | |
dc.creator | Peñaloza-Amion M. | |
dc.creator | Veas R. | |
dc.creator | Valenzuela-Barra G. | |
dc.creator | Zapata G. | |
dc.creator | Delogu G. | |
dc.creator | Uriarte E. | |
dc.creator | Santana L. | |
dc.creator | Olea-Azar C. | |
dc.creator | Delporte C. | |
dc.date.accessioned | 2020-09-02T22:18:16Z | |
dc.date.accessioned | 2022-11-08T20:26:43Z | |
dc.date.available | 2020-09-02T22:18:16Z | |
dc.date.available | 2022-11-08T20:26:43Z | |
dc.date.created | 2020-09-02T22:18:16Z | |
dc.date.issued | 2018 | |
dc.identifier | 18, 27, 2327-2337 | |
dc.identifier | 15680266 | |
dc.identifier | https://hdl.handle.net/20.500.12728/4559 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/5146160 | |
dc.language | en | |
dc.publisher | Bentham Science Publishers B.V. | |
dc.subject | Coumarins | |
dc.subject | Diabetes mellitus | |
dc.subject | Dmt2 | |
dc.subject | Docking studies | |
dc.subject | Medicinal chemistry | |
dc.subject | Α-(1,4)-glucosidase inhibition | |
dc.subject | 3 (4 bromothiophen 2 yl) 6 hydroxycoumarin | |
dc.subject | 3 (4 bromothiophen 2 yl) coumarin | |
dc.subject | 4 chloro n (7 hydroxy 4 methoxycoumarin 8 yl)benzamide | |
dc.subject | acarbose | |
dc.subject | alpha (1,4) glucosidase | |
dc.subject | alpha glucosidase | |
dc.subject | alpha glucosidase inhibitor | |
dc.subject | antidiabetic agent | |
dc.subject | coumarin derivative | |
dc.subject | hydrogen | |
dc.subject | n (4 hydroxycoumarin 3 yl) 4 methoxybenzamide | |
dc.subject | n (4 hydroxycoumarin 3 yl)acetamide | |
dc.subject | n (7 hydroxy 4 methylcoumarin 8 yl) 4 nitrobenzamide | |
dc.subject | n (7 hydroxy 4 methylcoumarin 8 yl) nicotinamide | |
dc.subject | n (7 hydroxy 4 methylcoumarin 8 yl)benzamide | |
dc.subject | phenylalanine | |
dc.subject | Saccharomyces cerevisiae protein | |
dc.subject | unclassified drug | |
dc.subject | coumarin derivative | |
dc.subject | glucan 1,4 alpha glucosidase | |
dc.subject | glycosidase inhibitor | |
dc.subject | Article | |
dc.subject | chemical interaction | |
dc.subject | controlled study | |
dc.subject | drug potency | |
dc.subject | drug structure | |
dc.subject | drug synthesis | |
dc.subject | drug targeting | |
dc.subject | enzyme active site | |
dc.subject | enzyme inhibition | |
dc.subject | hydrogen bond | |
dc.subject | hydrophobicity | |
dc.subject | in vitro study | |
dc.subject | molecular docking | |
dc.subject | non insulin dependent diabetes mellitus | |
dc.subject | Saccharomyces cerevisiae | |
dc.subject | antagonists and inhibitors | |
dc.subject | chemical structure | |
dc.subject | chemistry | |
dc.subject | dose response | |
dc.subject | enzymology | |
dc.subject | human | |
dc.subject | metabolism | |
dc.subject | non insulin dependent diabetes mellitus | |
dc.subject | structure activity relation | |
dc.subject | Coumarins | |
dc.subject | Diabetes Mellitus, Type 2 | |
dc.subject | Dose-Response Relationship, Drug | |
dc.subject | Glucan 1,4-alpha-Glucosidase | |
dc.subject | Glycoside Hydrolase Inhibitors | |
dc.subject | Humans | |
dc.subject | Molecular Structure | |
dc.subject | Structure-Activity Relationship | |
dc.title | Targeting α -(1,4)-glucosidase in diabetes mellitus type 2: The role of new synthetic coumarins as potent inhibitors | |
dc.type | Article | |