Detalhe da pesquisa
1.
Attenuation of Streptozotocin-Induced Diabetic Neuropathic Allodynia by Flavone Derivative Through Modulation of GABA-ergic Mechanisms and Endogenous Biomarkers.
Neurochem Res
; 49(4): 980-997, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38170385
2.
Synthesis, biochemical and computational evaluations of novel bis-acylhydrazones of 2,2'-(1,1'-biphenyl)-4,4'-diylbis(oxy))di(acetohydrazide) as dual cholinesterase inhibitors.
Bioorg Chem
; 144: 107144, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38281382
3.
Synthesis of 3-hydroxy-2-naphthohydrazide-based hydrazones and their implications in diabetic management via in vitro and in silico approaches.
Arch Pharm (Weinheim)
; 357(2): e2300544, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38013251
4.
A High Dose of Calcitriol Inhibits Glycolysis and M2 Macrophage Polarization in the Tumor Microenvironment by Repressing mTOR Activation: in vitro and Molecular Docking Studies.
Cell Physiol Biochem
; 57(2): 105-122, 2023 Apr 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37052042
5.
Synthesis, biological evaluation, and molecular docking study of chromen-linked hydrazine carbothioamides as potent α-glucosidase inhibitors.
Drug Dev Res
; 84(5): 962-974, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37186392
6.
Isoxazole analogues of dibenzazepine as possible leads against ulcers and skin disease: In vitro and in silico exploration.
Saudi Pharm J
; 31(12): 101877, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38075546
7.
Novel Bis-Schiff's base derivatives of 4-nitroacetophenone as potent α-glucosidase agents: Design, synthesis and in silico approach.
Bioorg Chem
; 128: 106058, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35917750
8.
Synthesis of novel hybrid pharmacophore of N-((4-sulfamoylphenyl)carbamothioyl)alkanamides as potent carbonic anhydrase-II and 15-lipoxygenase inhibitors.
Drug Dev Res
; 83(3): 745-754, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34897776
9.
Design, Synthesis and Molecular Docking Study of Novel 3-Phenyl-ß-Alanine-Based Oxadiazole Analogues as Potent Carbonic Anhydrase II Inhibitors.
Molecules
; 27(3)2022 Jan 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-35164091
10.
Microscale Thermophoresis and Molecular Modelling to Explore the Chelating Drug Transportation in the Milk to Infant.
Molecules
; 27(14)2022 Jul 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-35889479
11.
Therapeutic potential of N4-substituted thiosemicarbazones as new urease inhibitors: Biochemical and in silico approach.
Bioorg Chem
; 109: 104691, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33601138
12.
New Carbonic Anhydrase-II Inhibitors from Marine Macro Brown Alga Dictyopteris hoytii Supported by In Silico Studies.
Molecules
; 26(23)2021 Nov 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34885658
13.
Biomedical Applications of Scutellaria edelbergii Rech. f.: In Vitro and In Vivo Approach.
Molecules
; 26(12)2021 Jun 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-34205312
14.
Robust therapeutic potential of carbazole-triazine hybrids as a new class of urease inhibitors: A distinctive combination of nitrogen-containing heterocycles.
Bioorg Chem
; 95: 103479, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31901517
15.
Synthesis, characterization and molecular docking of some novel hydrazonothiazolines as urease inhibitors.
Bioorg Chem
; 94: 103404, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31699392
16.
Photocatalytic Decolorization and Biocidal Applications of Nonmetal Doped TiO2: Isotherm, Kinetic Modeling and In Silico Molecular Docking Studies.
Molecules
; 25(19)2020 Sep 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33003312
17.
Developing new hybrid scaffold for urease inhibition based on carbazole-chalcone conjugates: Synthesis, assessment of therapeutic potential and computational docking analysis.
Bioorg Med Chem
; 27(22): 115123, 2019 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31623971
18.
Synthesis of novel (R)-4-fluorophenyl-1H-1,2,3-triazoles: A new class of α-glucosidase inhibitors.
Bioorg Chem
; 91: 103182, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31404793
19.
Synthesis and characterization of new thiosemicarbazones, as potent urease inhibitors: In vitro and in silico studies.
Bioorg Chem
; 87: 155-162, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30884309
20.
Inhibitory Effects of Myrtucommuacetalone 1 (MCA-1) from Myrtus communis on Inflammatory Response in Mouse Macrophages.
Molecules
; 25(1)2019 Dec 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-31861488