604 related articles for article (PubMed ID: 33249154)
1. Utilization of the common functional groups in bioactive molecules: Exploring dual inhibitory potential and computational analysis of keto esters against α-glucosidase and carbonic anhydrase-II enzymes.
Khan I; Khan A; Halim SA; Khan M; Zaib S; Al-Yahyaei BEM; Al-Harrasi A; Ibrar A
Int J Biol Macromol; 2021 Jan; 167():233-244. PubMed ID: 33249154
[TBL] [Abstract][Full Text] [Related]
2. Probing benzenesulfonamide-thiazolidinone hybrids as multitarget directed ligands for efficient control of type 2 diabetes mellitus through targeting the enzymes: α-glucosidase and carbonic anhydrase II.
Gamal MA; Fahim SH; Giovannuzzi S; Fouad MA; Bonardi A; Gratteri P; Supuran CT; Hassan GS
Eur J Med Chem; 2024 May; 271():116434. PubMed ID: 38653067
[TBL] [Abstract][Full Text] [Related]
3. Synthesis of diethyl 4-substituted-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylates as a new series of inhibitors against yeast α-glucosidase.
Niaz H; Kashtoh H; Khan JA; Khan A; Wahab AT; Alam MT; Khan KM; Perveen S; Choudhary MI
Eur J Med Chem; 2015 May; 95():199-209. PubMed ID: 25817770
[TBL] [Abstract][Full Text] [Related]
4. Synthesis, characterization, inhibition effects, and molecular docking studies as acetylcholinesterase, α-glycosidase, and carbonic anhydrase inhibitors of novel benzenesulfonamides incorporating 1,3,5-triazine structural motifs.
Lolak N; Akocak S; Türkeş C; Taslimi P; Işık M; Beydemir Ş; Gülçin İ; Durgun M
Bioorg Chem; 2020 Jul; 100():103897. PubMed ID: 32413628
[TBL] [Abstract][Full Text] [Related]
5. Synthesis, Biological Evaluation and Molecular Docking Study of 2-Substituted-4,6-Diarylpyrimidines as α-Glucosidase Inhibitors.
Gong Z; Xie Z; Qiu J; Wang G
Molecules; 2017 Oct; 22(11):. PubMed ID: 29084182
[TBL] [Abstract][Full Text] [Related]
6. Biology-oriented drug synthesis and evaluation of secnidazole esters as novel enzyme ınhibitors.
Ansari MA; Saad SM; Khan KM; Salar U; Taslimi P; Taskın-Tok T; Saleem F; Jahangir S
Arch Pharm (Weinheim); 2022 Feb; 355(2):e2100376. PubMed ID: 34862640
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Oxadiazoles and thiadiazoles: novel α-glucosidase inhibitors.
Kashtoh H; Hussain S; Khan A; Saad SM; Khan JA; Khan KM; Perveen S; Choudhary MI
Bioorg Med Chem; 2014 Oct; 22(19):5454-65. PubMed ID: 25151088
[TBL] [Abstract][Full Text] [Related]
9. Synthesis, in vitro biological activities and in silico study of dihydropyrimidines derivatives.
Barakat A; Islam MS; Al-Majid AM; Ghabbour HA; Fun HK; Javed K; Imad R; Yousuf S; Choudhary MI; Wadood A
Bioorg Med Chem; 2015 Oct; 23(20):6740-8. PubMed ID: 26381063
[TBL] [Abstract][Full Text] [Related]
10. Synthesis, In vitro α-Glucosidase Inhibitory Potential and Molecular Docking Studies of 2-Amino-1,3,4-Oxadiazole Derivatives.
Ullah H; Rahim F; Taha M; Hussain R; Wadood A; Nawaz M; Wahab Z; Kanwal ; Khan KM
Med Chem; 2020; 16(6):724-734. PubMed ID: 31195948
[TBL] [Abstract][Full Text] [Related]
11. Synthesis, in vitro evaluation and molecular docking studies of novel coumarin-isatin derivatives as α-glucosidase inhibitors.
Wang G; Wang J; He D; Li X; Li J; Peng Z
Chem Biol Drug Des; 2017 Mar; 89(3):456-463. PubMed ID: 27616456
[TBL] [Abstract][Full Text] [Related]
12. Synthesis and biological evaluation of chepraecoxin A derivatives as α-glucosidase inhibitors.
Yang XT; Geng CA; Li TZ; Deng ZT; Chen JJ
Bioorg Med Chem Lett; 2020 Apr; 30(8):127020. PubMed ID: 32067867
[TBL] [Abstract][Full Text] [Related]
13. Synthesis of sulfonamide, amide and amine hybrid pharmacophore, an entry of new class of carbonic anhydrase II inhibitors and evaluation of chemo-informatics and binding analysis.
Ahmed A; Channar PA; Saeed A; Kalesse M; Kazi MA; Larik FA; Abbas Q; Hassan M; Raza H; Seo SY
Bioorg Chem; 2019 May; 86():624-630. PubMed ID: 30807935
[TBL] [Abstract][Full Text] [Related]
14. Inhibitory activity evaluation and mechanistic studies of tetracyclic oxindole derivatives as α-glucosidase inhibitors.
Sun H; Zhang Y; Ding W; Zhao X; Song X; Wang D; Li Y; Han K; Yang Y; Ma Y; Wang R; Wang D; Yu P
Eur J Med Chem; 2016 Nov; 123():365-378. PubMed ID: 27487567
[TBL] [Abstract][Full Text] [Related]
15. Synthesis and biological evaluation of novel tris-chalcones as potent carbonic anhydrase, acetylcholinesterase, butyrylcholinesterase and α-glycosidase inhibitors.
Burmaoglu S; Yilmaz AO; Polat MF; Kaya R; Gulcin İ; Algul O
Bioorg Chem; 2019 Apr; 85():191-197. PubMed ID: 30622011
[TBL] [Abstract][Full Text] [Related]
16. In vitro inhibitory effects of some acetophenone derivatives on some metabolic enzymes and molecular docking.
Taslimi P
Arch Pharm (Weinheim); 2020 Nov; 353(11):e2000210. PubMed ID: 32876951
[TBL] [Abstract][Full Text] [Related]
17. Synthesis and biological evaluation of coumarin derivatives as α-glucosidase inhibitors.
Xu XT; Deng XY; Chen J; Liang QM; Zhang K; Li DL; Wu PP; Zheng X; Zhou RP; Jiang ZY; Ma AJ; Chen WH; Wang SH
Eur J Med Chem; 2020 Mar; 189():112013. PubMed ID: 31972390
[TBL] [Abstract][Full Text] [Related]
18. Discovery of Amide-Functionalized Benzimidazolium Salts as Potent α-Glucosidase Inhibitors.
Khan IA; Ahmad M; Ashfaq UA; Sultan S; Zaki MEA
Molecules; 2021 Aug; 26(16):. PubMed ID: 34443347
[TBL] [Abstract][Full Text] [Related]
19. Design and synthesis of new imidazo[1,2-b]pyrazole derivatives, in vitro α-glucosidase inhibition, kinetic and docking studies.
Peytam F; Adib M; Shourgeshty R; Mohammadi-Khanaposhtani M; Jahani M; Imanparast S; Faramarzi MA; Mahdavi M; Moghadamnia AA; Rastegar H; Larijani B
Mol Divers; 2020 Feb; 24(1):69-80. PubMed ID: 30825061
[TBL] [Abstract][Full Text] [Related]
20. Pharmacophores Modeling in Terms of Prediction of Theoretical Physicochemical Properties and Verification by EXPERIMENTAL correlations of Carbacylamidophosphates (CAPh) and Sulfanylamidophosphates (SAPh) Tested as New Carbonic Anhydrase Inhibitors.
Amirkhanov V; Rauf A; Hadda TB; Ovchynnikov V; Trush V; Saleem M; Raza M; Rehman T; Zgou H; Shaheen U; Farghaly TA
Mini Rev Med Chem; 2019; 19(12):1015-1027. PubMed ID: 30806314
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
