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α-Mangostin Improves Glucose Uptake and Inhibits Adipocytes Differentiation in 3T3-L1 Cells via PPARγ, GLUT4, and Leptin Expressions.Antibacterial efficacy of the seed extracts of Melia azedarach against some hospital isolated human pathogenic bacterial strains.Averrhoa bilimbi Linn.: A review of its ethnomedicinal uses, phytochemistry, and pharmacology.Flavonoids from Tetracera indica Merr. induce adipogenesis and exert glucose uptake activities in 3T3-L1 adipocyte cells.Antifungal activity of Andrographis paniculata extracts and active principles against skin pathogenic fungal strains in vitro.Antioxidant and Antidiabetic Effects of Flavonoids: A Structure-Activity Relationship Based Study.A new sulphated flavone and other phytoconstituents from the leaves of Tetracera indica Merr. and their alpha-glucosidase inhibitory activity.Animal models and natural products to investigate in vivo and in vitro antidiabetic activity.Antiradical and Xanthine Oxidase Inhibitory Activity Evaluations of L. Leaves and Tentative Identification of Bioactive Constituents through LC-QTOF-MS/MS and Molecular Docking ApproachA simple method for extracting both active oily and water soluble extract (WSE) from Nigella sativa (L.) seeds using a single solvent systemStructure, degradation, drug release and mechanical properties relationships of iron-based drug eluting scaffolds: The effects of PLGACharacterization of α-Glucosidase Inhibitors from Lindau Leaves by Gas Chromatography-Mass Spectrometry-Based Metabolomics and Molecular Docking SimulationAntinociceptive activity of petroleum ether fraction obtained from methanolic extract of Clinacanthus nutans leaves involves the activation of opioid receptors and NO-mediated/cGMP-independent pathwayEvaluation of the Enzyme Inhibitory and Antioxidant Activities of Stem Bark and Isolation of the Active ConstituentsSynthesis of Thymidine Phosphorylase Inhibitor Based on Quinoxaline Derivatives and Their Molecular Docking StudyHystrix brachyura Bezoar Characterization, Antioxidant Activity Screening, and Anticancer Activity on Melanoma Cells (A375): A Preliminary StudySynthesis of Chromen-4-One-Oxadiazole Substituted Analogs as Potent -Glucuronidase InhibitorsOptimization of Hyperglycemic Induction in Zebrafish and Evaluation of Its Blood Glucose Level and Metabolite Fingerprint Treated with Jack Leaf ExtractMethylation and Acetylation Enhanced the Antidiabetic Activity of Some Selected Flavonoids: In Vitro, Molecular Modelling and Structure Activity Relationship-Based StudyBeneficial effect of the leaves of Murraya koenigii (Linn.) Spreng (Rutaceae) on diabetes-induced renal damage in vivoInvestigation of α-Glucosidase Inhibitory Metabolites from Tetracera scandens Leaves by GC-MS Metabolite Profiling and Docking StudiesIdentification of α-glucosidase inhibitors from Clinacanthus nutans leaf extract using liquid chromatography-mass spectrometry-based metabolomics and protein-ligand interaction with molecular dockingIn vivo anxiolytic and in vitro anti-inflammatory activities of water-soluble extract (WSE) of Nigella sativa (L.) seedsSynthesis of new isoquinoline-base-oxadiazole derivatives as potent inhibitors of thymidine phosphorylase and molecular docking studyThe promise of zebrafish as a model of metabolic syndromeToxicity study on Clinacanthus nutans leaf hexane fraction using Danio rerio embryosAnticancer activity of grassy Hystrix brachyura bezoar and its mechanisms of action: An in vitro and in vivo based studyIsolation and characterization of novel antibacterial compound from an untapped plant, Stereospermum fimbriatum
P50
Q35271424-2C1192D1-C5F2-41D6-93BF-F9FFA7BA1FC9Q36734199-B5D19C00-BCDE-4C1A-8709-AC478F211753Q38755449-281323EA-EA25-44BC-ADC4-6D1231D9360CQ41571708-0052CBC4-E352-4380-9A5A-EF1FFD27EA2EQ46228226-356C7659-7E69-494C-89CC-0AF3B495E920Q48274962-A13CBD45-A8E3-4BEB-8053-705F4888DA0FQ50124254-E5F687C8-14A2-4BCC-940A-AF9304B0472CQ52595760-052C1438-E2B5-4B5F-8B84-A92C11876237Q57293305-A5605757-BC29-4E88-9A05-C1E8FDCF4B58Q57928663-A18F03B6-97A5-4416-82C3-D870B5A7C819Q58227697-E2AA2C0E-B35E-44EC-A147-4B4B06D34A99Q58696295-1BADF41A-478F-41A8-B840-3CF9D43A085FQ64083410-D852EE30-AA38-4391-A166-81074E72291BQ64099043-A05BDFAE-BE7C-459E-B2AF-95904BECC05CQ64099058-AB2B72FC-FC19-4665-A9E0-E855D8B4EFBEQ64243706-993854A2-2C2B-4B01-969C-DDABC05AB910Q64249595-BFDB7E69-DDA0-4CBC-99CC-44CA404F4A4BQ64252546-29A2387D-4EFD-463F-85FC-F3C3687E9D6CQ64354354-E3A67E86-3047-49CC-8B44-E2A84A4565DCQ83482397-43DC3E23-710A-4570-8A37-A5865E4ECD8BQ89719848-D9972D4D-C248-47EC-8E3C-5674746AA8EAQ90217414-C2CFBB26-247B-4E86-98A4-DDA2FE80129FQ90444633-287EFBC1-57B3-4107-B2BA-45D795FEAC8EQ91130224-B34ACCB4-0DC3-4517-B20C-0BF3F6B448E5Q92226320-FCBECA8E-5F75-4BC9-9CBF-0DC1812812D7Q93016205-B7C7C7A8-321B-45C2-993D-2B7490EA8289Q93072395-1FCBA094-E297-48BC-A53B-8C06A4425062Q93332268-B0443759-3F4A-4C72-8904-951E7AFEB0F2
P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0003-0565-3222
@en
name
Qamar Uddin Ahmed
@ast
Qamar Uddin Ahmed
@en
Qamar Uddin Ahmed
@es
Qamar Uddin Ahmed
@nl
type
label
Qamar Uddin Ahmed
@ast
Qamar Uddin Ahmed
@en
Qamar Uddin Ahmed
@es
Qamar Uddin Ahmed
@nl
prefLabel
Qamar Uddin Ahmed
@ast
Qamar Uddin Ahmed
@en
Qamar Uddin Ahmed
@es
Qamar Uddin Ahmed
@nl
P106
P1153
14059640600
57194007453
P31
P496
0000-0003-0565-3222