178 related articles for article (PubMed ID: 25462626)
1. Organocatalyzed solvent free an efficient novel synthesis of 2,4,5-trisubstituted imidazoles for α-glucosidase inhibition to treat diabetes.
Yar M; Bajda M; Shahzad S; Ullah N; Gilani MA; Ashraf M; Rauf A; Shaukat A
Bioorg Chem; 2015 Feb; 58():65-71. PubMed ID: 25462626
[TBL] [Abstract][Full Text] [Related]
2. Novel synthesis of dihydropyrimidines for α-glucosidase inhibition to treat type 2 diabetes: in vitro biological evaluation and in silico docking.
Yar M; Bajda M; Shahzadi L; Shahzad SA; Ahmed M; Ashraf M; Alam U; Khan IU; Khan AF
Bioorg Chem; 2014 Jun; 54():96-104. PubMed ID: 24880489
[TBL] [Abstract][Full Text] [Related]
3. Triazinoindole analogs as potent inhibitors of α-glucosidase: synthesis, biological evaluation and molecular docking studies.
Rahim F; Ullah K; Ullah H; Wadood A; Taha M; Ur Rehman A; uddin I; Ashraf M; Shaukat A; Rehman W; Hussain S; Khan KM
Bioorg Chem; 2015 Feb; 58():81-7. PubMed ID: 25528720
[TBL] [Abstract][Full Text] [Related]
4. Organocatalyzed Novel Synthetic Methodology for Highly Functionalized Piperidines as Potent α-Glucosidase Inhibitors.
Farooq A; Shahazadi L; Bajda M; Ullah N; Rauf A; Shahzad SA; Khan AF; Ashraf M; Yar M
Arch Pharm (Weinheim); 2016 Sep; 349(9):724-32. PubMed ID: 27489132
[TBL] [Abstract][Full Text] [Related]
5. Organocatalyzed Solvent Free and Efficient Synthesis of 2,4,5-Trisubstituted Imidazoles as Potential Acetylcholinesterase Inhibitors for Alzheimer's Disease.
Pervaiz S; Mutahir S; Ullah I; Ashraf M; Liu X; Tariq S; Zhou BJ; Khan MA
Chem Biodivers; 2020 Mar; 17(3):e1900493. PubMed ID: 31968151
[TBL] [Abstract][Full Text] [Related]
6. In search of new α-glucosidase inhibitors: Imidazolylpyrazole derivatives.
Chaudhry F; Naureen S; Huma R; Shaukat A; Al-Rashida M; Asif N; Ashraf M; Munawar MA; Khan MA
Bioorg Chem; 2017 Apr; 71():102-109. PubMed ID: 28160945
[TBL] [Abstract][Full Text] [Related]
7. Synthesis, in vitro evaluation and molecular docking studies of novel triazine-triazole derivatives as potential α-glucosidase inhibitors.
Wang G; Peng Z; Wang J; Li X; Li J
Eur J Med Chem; 2017 Jan; 125():423-429. PubMed ID: 27689725
[TBL] [Abstract][Full Text] [Related]
8. Synthesis and biological evaluation of novel 2,4,5-triarylimidazole-1,2,3-triazole derivatives via click chemistry as α-glucosidase inhibitors.
Wang G; Peng Z; Wang J; Li J; Li X
Bioorg Med Chem Lett; 2016 Dec; 26(23):5719-5723. PubMed ID: 27810241
[TBL] [Abstract][Full Text] [Related]
9. Synthesis and molecular docking studies of potent α-glucosidase inhibitors based on biscoumarin skeleton.
Khan KM; Rahim F; Wadood A; Kosar N; Taha M; Lalani S; Khan A; Fakhri MI; Junaid M; Rehman W; Khan M; Perveen S; Sajid M; Choudhary MI
Eur J Med Chem; 2014 Jun; 81():245-52. PubMed ID: 24844449
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Synthesis, molecular docking studies of hybrid benzimidazole as α-glucosidase inhibitor.
Zawawi NK; Taha M; Ahmat N; Ismail NH; Wadood A; Rahim F
Bioorg Chem; 2017 Feb; 70():184-191. PubMed ID: 28043716
[TBL] [Abstract][Full Text] [Related]
12. Synthesis, molecular docking and α-glucosidase inhibition of 2-((5,6-diphenyl-1,2,4-triazin-3-yl)thio)-N-arylacetamides.
Wang G; Li X; Wang J; Xie Z; Li L; Chen M; Chen S; Peng Y
Bioorg Med Chem Lett; 2017 Mar; 27(5):1115-1118. PubMed ID: 28189421
[TBL] [Abstract][Full Text] [Related]
13. Synthesis of novel inhibitors of α-glucosidase based on the benzothiazole skeleton containing benzohydrazide moiety and their molecular docking studies.
Taha M; Ismail NH; Lalani S; Fatmi MQ; Atia-Tul-Wahab ; Siddiqui S; Khan KM; Imran S; Choudhary MI
Eur J Med Chem; 2015 Mar; 92():387-400. PubMed ID: 25585009
[TBL] [Abstract][Full Text] [Related]
14. Imidazole-pyrazole hybrids: Synthesis, characterization and in-vitro bioevaluation against α-glucosidase enzyme with molecular docking studies.
Chaudhry F; Naureen S; Ashraf M; Al-Rashida M; Jahan B; Munawar MA; Khan MA
Bioorg Chem; 2019 Feb; 82():267-273. PubMed ID: 30396060
[TBL] [Abstract][Full Text] [Related]
15. Design, synthesis and docking study of novel tetracyclic oxindole derivatives as α-glucosidase inhibitors.
Han K; Li Y; Zhang Y; Teng Y; Ma Y; Wang M; Wang R; Xu W; Yao Q; Zhang Y; Qin H; Sun H; Yu P
Bioorg Med Chem Lett; 2015 Apr; 25(7):1471-5. PubMed ID: 25759031
[TBL] [Abstract][Full Text] [Related]
16. Biological evaluation of new imidazole derivatives tethered with indole moiety as potent α-glucosidase inhibitors.
Naureen S; Chaudhry F; Munawar MA; Ashraf M; Hamid S; Khan MA
Bioorg Chem; 2018 Feb; 76():365-369. PubMed ID: 29232634
[TBL] [Abstract][Full Text] [Related]
17. Isatin based Schiff bases as inhibitors of α-glucosidase: Synthesis, characterization, in vitro evaluation and molecular docking studies.
Rahim F; Malik F; Ullah H; Wadood A; Khan F; Javid MT; Taha M; Rehman W; Ur Rehman A; Khan KM
Bioorg Chem; 2015 Jun; 60():42-8. PubMed ID: 25955493
[TBL] [Abstract][Full Text] [Related]
18. Synthesis of novel indenoquinoxaline derivatives as potent α-glucosidase inhibitors.
Khan MS; Munawar MA; Ashraf M; Alam U; Ata A; Asiri AM; Kousar S; Khan MA
Bioorg Med Chem; 2014 Feb; 22(3):1195-200. PubMed ID: 24398385
[TBL] [Abstract][Full Text] [Related]
19. 2-Arylquinazolin-4(3H)-ones: A new class of α-glucosidase inhibitors.
Javaid K; Saad SM; Rasheed S; Moin ST; Syed N; Fatima I; Salar U; Khan KM; Perveen S; Choudhary MI
Bioorg Med Chem; 2015 Dec; 23(23):7417-21. PubMed ID: 26552899
[TBL] [Abstract][Full Text] [Related]
20. Synthesis, α-glucosidase inhibitory and molecular docking studies of prenylated and geranylated flavones, isoflavones and chalcones.
Sun H; Li Y; Zhang X; Lei Y; Ding W; Zhao X; Wang H; Song X; Yao Q; Zhang Y; Ma Y; Wang R; Zhu T; Yu P
Bioorg Med Chem Lett; 2015 Oct; 25(20):4567-71. PubMed ID: 26351039
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]