Vitexin and isovitexin from the Leaves of Ficus deltoidea with in-vivo α-glucosidase inhibition

QR Code

Vitexin and isovitexin from the Leaves of Ficus deltoidea with in-vivo α-glucosidase inhibition

Ethnopharmacological relevance: The leaves of Ficus deltoidea are used as a traditional medicine by diabetes patients in Malaysia. Aim of the study: The objective of the study is to identify and evaluate bioactive constituents with in vivo α-glucosidase inhibition. Materials and Methods: The partiti...

書目詳細資料
發表在:	Journal of Ethnopharmacology
主要作者:	2-s2.0-84863985161
格式:	Article
語言:	English
出版:	2012
在線閱讀:	https://www.scopus.com/inward/record.uri?eid=2-s2.0-84863985161&doi=10.1016%2fj.jep.2012.05.062&partnerID=40&md5=ce0eb29006e96da3dfcafa2bf3a0ddfd

相似書籍

Chemical mediators of pollinator specificity breakdown in dioecious Ficus deltoidea complex
由: 2-s2.0-85213999414
出版: (2025)

Chemical characterizations dataset of flavonoid glycoside isomers and other constituents from Ficus deltoidea Jack
由: 2-s2.0-85190976576
出版: (2024)

Chemical mediators of pollinator specificity breakdown in dioecious Ficus deltoidea complex
由: Nizam, et al.
出版: (2025)

Chemical mediators of pollinator specificity breakdown in dioecious Ficus deltoidea complex
由: Nizam N.‘.; Naser N.B.M.; Yahaya I.N.S.; Rashid R.A.; Kasim N.; Nudin N.F.H.; Hatta S.K.M.
出版: (2025)

Synthesis, α-glucosidase inhibition and molecular docking study of coumarin based derivatives
由: 2-s2.0-85042298379
出版: (2018)

Ficus deltoidea ameliorates biochemical, hormonal, and histomorphometric changes in letrozole-induced polycystic ovarian syndrome rats
由: 2-s2.0-85120170860
出版: (2021)

Synthesis of novel flavone hydrazones: In-vitro evaluation of α-glucosidase inhibition, QSAR analysis and docking studies
由: 2-s2.0-84944728488
出版: (2015)

Ficus deltoidea standardized methanolic extract improves kidney structure and function against streptozotocin-induced diabetic nephropathy in rats
由: Samsulrizal N.; Zin N.S.N.M.; Syimal`ain Azmi N.; Bakar M.D.; Ahmad H.; Goh Y.-M.
出版: (2025)

Synthesis, characterization, antibacterial, α-glucosidase inhibition and hemolytic studies on some new n-(2,3-Dimethylphenyl)benzenesulfonamide derivatives
由: 2-s2.0-84962385188
出版: (2016)

Antioxidant and α-glucosidase inhibitory constituents from Hornstedtia species of Malaysia
由: Hashim S.E.; Sirat H.M.; Yen K.H.; Ismail I.S.; Matsuki S.N.
出版: (2015)

Synthesis of new oxadiazole derivatives as α-glucosidase inhibitors
由: 2-s2.0-84937512790
出版: (2015)

Synthesis of Flurbiprofen Based Amide Derivatives as Potential Leads for Diabetic Management: In Vitro α-glucosidase Inhibition, Molecular Docking and DFT Simulation Approach
由: 2-s2.0-85191891273
出版: (2024)

Benzimidazole derivatives as new α-glucosidase inhibitors and in silico studies
由: 2-s2.0-84948649641
出版: (2016)

Discovery of amide-functionalized benzimidazolium salts as potent α-glucosidase inhibitors
由: 2-s2.0-85112329694
出版: (2021)

Ficus deltoidea suppresses endothelial activation, inflammation, monocytes adhesion and oxidative stress via NF-κB and eNOS pathways in stimulated human coronary artery endothelial cells
由: 2-s2.0-85089582076
出版: (2020)

Synthesis of Indole Based Sulfonamide Derivatives as potent inhibitors of α-glucosidase and α-amylase in management of type-II diabetes
由: 2-s2.0-85185155619
出版: (2024)

Synthesis and Molecular Docking Study of Hydrazone Schiff Bases of α-Naphthalene-Containing Alkyl Phenyl Ether Fragment as Potent α-Amylase and α-Glucosidase Inhibitors
由: 2-s2.0-85208551606
出版: (2024)

Ficus deltoidea suppresses endothelial activation, inflammation, monocytes adhesion and oxidative stress via NF-κB and eNOS pathways in stimulated human coronary artery endothelial cells
由: Mohd Ariff A.; Abu Bakar N.A.; Abd Muid S.; Omar E.; Ismail N.H.; Ali A.M.; Mohd Kasim N.A.; Mohd Nawawi H.
出版: (2020)

Synthesis, in vitro α-glucosidase activity and in silico molecular docking study of isatin analogues
由: 2-s2.0-85146025150
出版: (2023)

Synthesis, in vitro α-glucosidase inhibitory potential and molecular docking study of thiadiazole analogs
由: 2-s2.0-85044438335
出版: (2018)

New benzoxazole-based sulphonamide hybrids analogs as potent inhibitors of α-amylase and α-glucosidase: Synthesis and in vitro evaluation along with in silico study
由: 2-s2.0-85140093344
出版: (2022)

Synthesis, in vitro α-glucosidase inhibitory activity and molecular docking studies of new thiazole derivatives
由: 2-s2.0-84984780886
出版: (2016)

Novel thiosemicarbazide-oxadiazole hybrids as unprecedented inhibitors of yeast α-glucosidase and in silico binding analysis
由: 2-s2.0-84964523904
出版: (2016)

Novel quinoline derivatives as potent in vitro α-glucosidase inhibitors: In silico studies and SAR predictions
由: 2-s2.0-84943771420
出版: (2015)

Molecular Modeling and Synthesis of Indoline-2,3-dione-Based Benzene Sulfonamide Derivatives and Their Inhibitory Activity against α-Glucosidase and α-Amylase Enzymes
由: 2-s2.0-85154584205
出版: (2023)

Synthesis of novel triazinoindole-based thiourea hybrid: A study on α-glucosidase inhibitors and their molecular docking
由: 2-s2.0-85074173138
出版: (2019)

Evaluation of 2-indolcarbohydrazones as potent α-glucosidase inhibitors, in silico studies and DFT based stereochemical predictions
由: 2-s2.0-84942794211
出版: (2015)

Synthesis, biological evaluation and molecular docking study of benzimidazole derivatives as α-glucosidase inhibitors and anti-diabetes candidates
由: 2-s2.0-85144315169
出版: (2023)

Syntheses of new 3-thiazolyl coumarin derivatives, in vitro α-glucosidase inhibitory activity, and molecular modeling studies
由: 2-s2.0-84976472588
出版: (2016)

Syntheses, in vitro evaluation and molecular docking studies of 5-bromo-2-aryl benzimidazoles as α-glucosidase inhibitors
由: 2-s2.0-84979210899
出版: (2016)

Isatin based Schiff bases as inhibitors of α-glucosidase: Synthesis, characterization, in vitro evaluation and molecular docking studies
由: 2-s2.0-84928815461
出版: (2015)

Styryl-lactone goniothalamin inhibits TNF-α-induced NF-κB activation
由: 2-s2.0-84881002603
出版: (2013)

Synthesis and biological evaluation of novel coumarin derivatives bearing sulfonamide moiety as potent α-glucosidase inhibitors
由: Alsukor A.; Inayatsyah N.A.; Ridhwan M.J.M.; Kasim N.; Imran S.
出版: (2025)

5-Bromo-2-aryl benzimidazole derivatives as non-cytotoxic potential dual inhibitors of α-glucosidase and urease enzymes
由: 2-s2.0-85016039331
出版: (2017)

Hydrazinyl arylthiazole based pyridine scaffolds: Synthesis, structural characterization, in vitro α-glucosidase inhibitory activity, and in silico studies
由: 2-s2.0-85021402072
出版: (2017)

Exploring Acyl Thiotriazinoindole Based Pharmacophores: Design, Synthesis, and SAR Studies with Molecular Docking and Biological Activity Profiling against Urease, α-amylase, α-glucosidase, Antimicrobial, and Antioxidant Targets
由: 2-s2.0-85202972638
出版: (2024)

Evaluation and docking of indole sulfonamide as a potent inhibitor of α-glucosidase enzyme in streptozotocin –induced diabetic albino wistar rats
由: 2-s2.0-85102849446
出版: (2021)

Α-Glucosidase inhibitory potential and hemolytic evaluation of newly synthesized 3, 4, 5-trisubstituted-1, 2, 4-triazole derivatives
由: 2-s2.0-85077924129
出版: (2019)

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
由: 2-s2.0-85025127822
出版: (2017)

In vivo antiulcer activity of the aqueous extract of Bauhinia purpurea leaf
由: 2-s2.0-80052035542
出版: (2011)