PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 33387581-3 2021 In this review, we discussed the antioxidant potential of chalcones and elucidated the mechanisms of pathways and proteins such as carbohydrate digestive enzymes (alpha-amylase and alpha-glucosidase), aldose reductase, SLGT-2, and Nrf2 that are targeted by antidiabetic chalcones. Chalcones 58-67 sucrase-isomaltase Homo sapiens 181-198 31808389-1 2021 BACKGROUND: Chalcones, originated from natural product, have been broadly studied their biological activity against various proteins which at the molecular level, are responsible for the progress of the diseases in cancer (e.g. kinases), inflammation (oxidoreductases), atherosclerosis (cathepsins receptor), and diabetes (e.g. alpha-glucosidase). Chalcones 12-21 sucrase-isomaltase Homo sapiens 328-345 28242551-0 2017 Analogues of xanthones--Chalcones and bis-chalcones as alpha-glucosidase inhibitors and anti-diabetes candidates. Chalcones 24-33 sucrase-isomaltase Homo sapiens 55-72 31414099-3 2019 In the present work, a panel of chalcones bearing hydroxy, methoxy, methyl, nitro, chloro, fluoro and bromo substituents were evaluated against alpha-amylase and alpha-glucosidase activities, most of them for the first time. Chalcones 32-41 sucrase-isomaltase Homo sapiens 162-179 31414099-6 2019 Chalcones holding nitro groups and chloro substituents, together with a hydroxy group in the chalcone scaffold, showed strong inhibition of the alpha-glucosidase activity. Chalcones 0-9 sucrase-isomaltase Homo sapiens 144-161 25638569-3 2015 Several natural and (semi) synthetic chalcones deserve the credit of being potential candidates that act by modulating the therapeutic targets PPAR-gamma, DPP-4, alpha-glucosidase, PTP1B, aldose reductase, and stimulate insulin secretion and tissue sensitivity. Chalcones 37-46 sucrase-isomaltase Homo sapiens 162-179 26351039-0 2015 Synthesis, alpha-glucosidase inhibitory and molecular docking studies of prenylated and geranylated flavones, isoflavones and chalcones. Chalcones 126-135 sucrase-isomaltase Homo sapiens 11-28 16202584-3 2005 In particular, sulfonamide chalcones 17-20 had more potent alpha-glucosidase inhibitory activity than aminated chalcone 13-16. Chalcones 27-36 sucrase-isomaltase Homo sapiens 59-76 17191997-2 2005 Both the benzothiazepines and chalcones were evaluated as DPPH free-radical scavengers and as inhibitors of cholinesterases, urease, and alpha-glucosidase. Chalcones 30-39 sucrase-isomaltase Homo sapiens 137-154