Detalles de la búsqueda
1.
Bioevaluation of synthetic pyridones as dual inhibitors of α-amylase and α-glucosidase enzymes and potential antioxidants.
Arch Pharm (Weinheim);
356(1): e2200400, 2023 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-36284484
2.
Dihydroquinazolin-4(1H)-one derivatives as novel and potential leads for diabetic management.
Mol Divers;
26(2): 849-868, 2022 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-33650031
3.
Biology-oriented drug synthesis (BIODS), in vitro urease inhibitory activity, and in silico studies on ibuprofen derivatives.
Mol Divers;
25(1): 143-157, 2021 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-31965436
4.
Indole acrylonitriles as potential anti-hyperglycemic agents: Synthesis, α-glucosidase inhibitory activity and molecular docking studies.
Bioorg Med Chem;
28(21): 115605, 2020 11 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33065441
5.
Syntheses, in vitro α-amylase and α-glucosidase dual inhibitory activities of 4-amino-1,2,4-triazole derivatives their molecular docking and kinetic studies.
Bioorg Med Chem;
28(11): 115467, 2020 06 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32327353
6.
Dihydropyridines as potential α-amylase and α-glucosidase inhibitors: Synthesis, in vitro and in silico studies.
Bioorg Chem;
96: 103581, 2020 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-31978686
7.
Synthesis of new indazole based dual inhibitors of α-glucosidase and α-amylase enzymes, their in vitro, in silico and kinetics studies.
Bioorg Chem;
94: 103195, 2020 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-31451297
8.
Indenoquinoxaline-phenylacrylohydrazide hybrids as promising drug candidates for the treatment of type 2 diabetes: In vitro and in silico evaluation of enzyme inhibition and antioxidant activity.
Int J Biol Macromol;
263(Pt 2): 129517, 2024 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-38266833
9.
Unsymmetrical thiourea derivatives: synthesis and evaluation as promising antioxidant and enzyme inhibitors.
Future Med Chem;
16(6): 497-511, 2024 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-38372209
10.
Development in the Inhibition of Dengue Proteases as Drug Targets.
Curr Med Chem;
2023 Sep 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-37723635
11.
Regioselective syntheses of 2-oxopyridine carbonitrile derivatives and evaluation for antihyperglycemic and antioxidant potential.
Int J Biol Macromol;
241: 124589, 2023 Jun 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-37116840
12.
Evaluation of synthetic aminoquinoline derivatives as urease inhibitors: in vitro, in silico and kinetic studies.
Future Med Chem;
15(18): 1703-1717, 2023 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-37814798
13.
Synthetic benzofuran-linked chalcones with dual actions: a potential therapeutic approach to manage diabetes mellitus.
Future Med Chem;
15(2): 167-187, 2023 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-36799245
14.
Synthetic piperidine-substituted chalcones as potential hits for α-amylase inhibitory and antioxidant activities.
Future Med Chem;
15(6): 497-515, 2023 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-37092302
15.
Hydrazinyl thiazole linked indenoquinoxaline hybrids: Potential leads to treat hyperglycemia and oxidative stress; Multistep synthesis, α-amylase, α-glucosidase inhibitory and antioxidant activities.
Int J Biol Macromol;
221: 1294-1312, 2022 Nov 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-36113601
16.
Evaluation of synthetic 2-aryl quinoxaline derivatives as α-amylase, α-glucosidase, acetylcholinesterase, and butyrylcholinesterase inhibitors.
Int J Biol Macromol;
211: 653-668, 2022 Jun 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-35568155
17.
Efficient one-pot synthesis of arylated pyrazole-fused pyran analogs: as leads to treating diabetes and Alzheimer's disease.
Future Med Chem;
14(21): 1507-1526, 2022 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-36268762
18.
Indane-1,3-diones: As Potential and Selective α-glucosidase Inhibitors, their Synthesis, in vitro and in silico Studies.
Med Chem;
17(8): 887-902, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-32851965
19.
Synthesis of benzotriazoles derivatives and their dual potential as α-amylase and α-glucosidase inhibitors in vitro: Structure-activity relationship, molecular docking, and kinetic studies.
Eur J Med Chem;
183: 111677, 2019 Dec 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-31514061
Resultados
1 -
19
de 19
1
Próxima >
>>