These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
241 related articles for article (PubMed ID: 30594450)
1. α-Glucosidase inhibition activity and in silico study of 2-(benzo[d][1,3]dioxol-5-yl)-4H-chromen-4-one, a synthetic derivative of flavone. Meena SN; Kumar U; Naik MM; Ghadi SC; Tilve SG Bioorg Med Chem; 2019 Jun; 27(12):2340-2344. PubMed ID: 30594450 [TBL] [Abstract][Full Text] [Related]
2. Comparative study of inhibition mechanisms of structurally different flavonoid compounds on α-glucosidase and synergistic effect with acarbose. Yang J; Wang X; Zhang C; Ma L; Wei T; Zhao Y; Peng X Food Chem; 2021 Jun; 347():129056. PubMed ID: 33476922 [TBL] [Abstract][Full Text] [Related]
3. Design, synthesis, molecular modelling, ADME prediction and anti-hyperglycemic evaluation of new pyrazole-triazolopyrimidine hybrids as potent α-glucosidase inhibitors. Pogaku V; Gangarapu K; Basavoju S; Tatapudi KK; Katragadda SB Bioorg Chem; 2019 Dec; 93():103307. PubMed ID: 31585262 [TBL] [Abstract][Full Text] [Related]
4. Novel Coumarin Containing Dithiocarbamate Derivatives as Potent α-Glucosidase Inhibitors for Management of Type 2 Diabetes. Mollazadeh M; Mohammadi-Khanaposhtani M; Valizadeh Y; Zonouzi A; Faramarzi MA; Kiani M; Biglar M; Larijani B; Hamedifar H; Mahdavi M; Hajimiri MH Med Chem; 2021; 17(3):264-272. PubMed ID: 32851964 [TBL] [Abstract][Full Text] [Related]
5. Pyrano[3,2-c]quinoline Derivatives as New Class of α-glucosidase Inhibitors to Treat Type 2 Diabetes: Synthesis, in vitro Biological Evaluation and Kinetic Study. Heydari Z; Mohammadi-Khanaposhtani M; Imanparast S; Faramarzi MA; Mahdavi M; Ranjbar PR; Larijani B Med Chem; 2019; 15(1):8-16. PubMed ID: 29807519 [TBL] [Abstract][Full Text] [Related]
6. Study on the Interaction of 1,5-diaryl Pyrrole Derivatives with α- glucosidase; Synthesis, Molecular Docking, and Kinetic Study. Tafesse TB; Moghadam ES; Bule MH; Faramarzi MA; Abdollahi M; Amini M Med Chem; 2021; 17(5):545-553. PubMed ID: 31808390 [TBL] [Abstract][Full Text] [Related]
7. Synthetic heterocyclic candidates as promising α-glucosidase inhibitors: An overview. Dhameja M; Gupta P Eur J Med Chem; 2019 Aug; 176():343-377. PubMed ID: 31112894 [TBL] [Abstract][Full Text] [Related]
8. Polyoxomolybdates as α-glucosidase inhibitors: Kinetic and molecular modeling studies. Chi G; Qi Y; Li J; Wang L; Hu J J Inorg Biochem; 2019 Apr; 193():173-179. PubMed ID: 30776576 [TBL] [Abstract][Full Text] [Related]
9. Design and synthesis of novel quinazolinone-1,2,3-triazole hybrids as new anti-diabetic agents: In vitro α-glucosidase inhibition, kinetic, and docking study. Saeedi M; Mohammadi-Khanaposhtani M; Pourrabia P; Razzaghi N; Ghadimi R; Imanparast S; Faramarzi MA; Bandarian F; Esfahani EN; Safavi M; Rastegar H; Larijani B; Mahdavi M; Akbarzadeh T Bioorg Chem; 2019 Mar; 83():161-169. PubMed ID: 30366316 [TBL] [Abstract][Full Text] [Related]
10. Discovery of new 2-phenyl-1H-benzo[d]imidazole core-based potent α-glucosidase inhibitors: Synthesis, kinetic study, molecular docking, and in vivo anti-hyperglycemic evaluation. Li Y; Zhang JH; Xie HX; Ge YX; Wang KM; Song ZL; Zhu KK; Zhang J; Jiang CS Bioorg Chem; 2021 Dec; 117():105423. PubMed ID: 34717239 [TBL] [Abstract][Full Text] [Related]
11. Dithiocarbamate derivatives inhibit α-glucosidase through an apparent allosteric site on the enzyme. Ghani U; Ashraf S; Ul-Haq Z; Mujamammi AH; Özkay Y; Demirci F; Kaplancikli ZA Chem Biol Drug Des; 2021 Aug; 98(2):283-294. PubMed ID: 34047492 [TBL] [Abstract][Full Text] [Related]
12. Indole acrylonitriles as potential anti-hyperglycemic agents: Synthesis, α-glucosidase inhibitory activity and molecular docking studies. Solangi M; Kanwal ; Mohammed Khan K; Saleem F; Hameed S; Iqbal J; Shafique Z; Qureshi U; Ul-Haq Z; Taha M; Perveen S Bioorg Med Chem; 2020 Nov; 28(21):115605. PubMed ID: 33065441 [TBL] [Abstract][Full Text] [Related]
13. Design, synthesis, in vitro, and in silico evaluations of benzo[d]imidazole-amide-1,2,3-triazole-N-arylacetamide hybrids as new antidiabetic agents targeting α-glucosidase. Yousefnejad F; Mohammadi-Moghadam-Goozali M; Sayahi MH; Halimi M; Moazzam A; Mohammadi-Khanaposhtani M; Mojtabavi S; Asadi M; Faramarzi MA; Larijani B; Amanlou M; Mahdavi M Sci Rep; 2023 Jul; 13(1):12397. PubMed ID: 37524733 [TBL] [Abstract][Full Text] [Related]
15. 2,4-Dichloro-5-[(N-aryl/alkyl)sulfamoyl]benzoic Acid Derivatives: In Vitro Antidiabetic Activity, Molecular Modeling and In silico ADMET Screening. Thakral S; Singh V Med Chem; 2019; 15(2):186-195. PubMed ID: 30251608 [TBL] [Abstract][Full Text] [Related]
16. Inhibitory mechanism of morin on α-glucosidase and its anti-glycation properties. Zeng L; Zhang G; Liao Y; Gong D Food Funct; 2016 Sep; 7(9):3953-63. PubMed ID: 27549567 [TBL] [Abstract][Full Text] [Related]
17. Inhibitory Activity and Mechanism Investigation of Hypericin as a Novel Dong Q; Hu N; Yue H; Wang H Molecules; 2021 Jul; 26(15):. PubMed ID: 34361714 [No Abstract] [Full Text] [Related]
18. Design, synthesis, and in silico studies of quinoline-based-benzo[d]imidazole bearing different acetamide derivatives as potent α-glucosidase inhibitors. Noori M; Davoodi A; Iraji A; Dastyafteh N; Khalili M; Asadi M; Mohammadi Khanaposhtani M; Mojtabavi S; Dianatpour M; Faramarzi MA; Larijani B; Amanlou M; Mahdavi M Sci Rep; 2022 Aug; 12(1):14019. PubMed ID: 35982225 [TBL] [Abstract][Full Text] [Related]
19. Potential of lignin from Canna edulis ker residue in the inhibition of α-d-glucosidase: Kinetics and interaction mechanism merging with docking simulation. Xie F; Gong S; Zhang W; Wu J; Wang Z Int J Biol Macromol; 2017 Feb; 95():592-602. PubMed ID: 27908712 [TBL] [Abstract][Full Text] [Related]
20. Synthesis of novel flavone hydrazones: in-vitro evaluation of α-glucosidase inhibition, QSAR analysis and docking studies. Imran S; Taha M; Ismail NH; Kashif SM; Rahim F; Jamil W; Hariono M; Yusuf M; Wahab H Eur J Med Chem; 2015 Nov; 105():156-70. PubMed ID: 26491979 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]