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1.
Synthesis of benzothiazole derivatives as a potent α-glucosidase inhibitor.
Bioorg Chem
; 85: 33-48, 2019 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-30599411
2.
Bisindolylmethane thiosemicarbazides as potential inhibitors of urease: Synthesis and molecular modeling studies.
Bioorg Med Chem
; 26(1): 152-160, 2018 01 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-29183662
3.
Synthesis, SAR elucidations and molecular docking study of newly designed isatin based oxadiazole analogs as potent inhibitors of thymidine phosphorylase.
Bioorg Chem
; 79: 323-333, 2018 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-29803079
4.
Synthesis, in vitro α-glucosidase inhibitory potential and molecular docking study of thiadiazole analogs.
Bioorg Chem
; 78: 201-209, 2018 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-29597114
5.
Synthesis of indole analogs as potent ß-glucuronidase inhibitors.
Bioorg Chem
; 72: 323-332, 2017 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-28505547
6.
Synthesis, α-glucosidase inhibitory activity and in silico study of tris-indole hybrid scaffold with oxadiazole ring: As potential leads for the management of type-II diabetes mellitus.
Bioorg Chem
; 74: 30-40, 2017 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-28750203
7.
Synthesis of alpha amylase inhibitors based on privileged indole scaffold.
Bioorg Chem
; 72: 248-255, 2017 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-28482265
8.
Biology-oriented drug synthesis (BIODS) of 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl ether derivatives, in vitro α-amylase inhibitory activity and in silico studies.
Bioorg Chem
; 74: 1-9, 2017 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-28719801
9.
Isatin based Schiff bases as inhibitors of α-glucosidase: Synthesis, characterization, in vitro evaluation and molecular docking studies.
Bioorg Chem
; 60: 42-8, 2015 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-25955493
10.
Synthesis, in vitro evaluation and molecular docking studies of thiazole derivatives as new inhibitors of α-glucosidase.
Bioorg Chem
; 62: 15-21, 2015 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-26162519
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