228 related articles for article (PubMed ID: 29860891)
1. The behavior of some chalcones on acetylcholinesterase and carbonic anhydrase activity.
Aslan HE; Demir Y; Özaslan MS; Türkan F; Beydemir Ş; Küfrevioğlu ÖI
Drug Chem Toxicol; 2019 Nov; 42(6):634-640. PubMed ID: 29860891
[TBL] [Abstract][Full Text] [Related]
2. Carbonic anhydrase and acetylcholinesterase inhibitory effects of carbamates and sulfamoylcarbamates.
Göçer H; Akincioğlu A; Göksu S; Gülçin İ; Supuran CT
J Enzyme Inhib Med Chem; 2015 Apr; 30(2):316-20. PubMed ID: 24964347
[TBL] [Abstract][Full Text] [Related]
3. Synthesis of chalcone-imide derivatives and investigation of their anticancer and antimicrobial activities, carbonic anhydrase and acetylcholinesterase enzymes inhibition profiles.
Kocyigit UM; Budak Y; Gürdere MB; Ertürk F; Yencilek B; Taslimi P; Gülçin İ; Ceylan M
Arch Physiol Biochem; 2018 Feb; 124(1):61-68. PubMed ID: 28792233
[TBL] [Abstract][Full Text] [Related]
4. Synthesis, characterization, and biological studies of chalcone derivatives containing Schiff bases: Synthetic derivatives for the treatment of epilepsy and Alzheimer's disease.
Koçyiğit ÜM; Gezegen H; Taslimi P
Arch Pharm (Weinheim); 2020 Dec; 353(12):e2000202. PubMed ID: 32815568
[TBL] [Abstract][Full Text] [Related]
5. The impact of hydroquinone on acetylcholine esterase and certain human carbonic anhydrase isoenzymes (hCA I, II, IX, and XII).
Scozzafava A; Kalın P; Supuran CT; Gülçin İ; Alwasel SH
J Enzyme Inhib Med Chem; 2015 Dec; 30(6):941-6. PubMed ID: 25586344
[TBL] [Abstract][Full Text] [Related]
6. Intermolecular amination of allylic and benzylic alcohols leads to effective inhibitions of acetylcholinesterase enzyme and carbonic anhydrase I and II isoenzymes.
Atmaca U; Yıldırım A; Taslimi P; Çelik ST; Gülçin İ; Supuran CT; Çelik M
J Biochem Mol Toxicol; 2018 Aug; 32(8):e22173. PubMed ID: 29975450
[TBL] [Abstract][Full Text] [Related]
7. Synthesis, biological evaluation and molecular docking of novel pyrazole derivatives as potent carbonic anhydrase and acetylcholinesterase inhibitors.
Turkan F; Cetin A; Taslimi P; Karaman M; Gulçin İ
Bioorg Chem; 2019 May; 86():420-427. PubMed ID: 30769267
[TBL] [Abstract][Full Text] [Related]
8. Novel eugenol derivatives: Potent acetylcholinesterase and carbonic anhydrase inhibitors.
Topal F; Gulcin I; Dastan A; Guney M
Int J Biol Macromol; 2017 Jan; 94(Pt B):845-851. PubMed ID: 27984137
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. In vitro inhibition effect of some chalcones on erythrocyte carbonic anhydrase I and II.
Gençer N; Bilen Ç; Demir D; Atahan A; Ceylan M; Küçükislamoğlu M
Artif Cells Nanomed Biotechnol; 2013 Dec; 41(6):384-8. PubMed ID: 23330659
[TBL] [Abstract][Full Text] [Related]
11. Synthesis of novel tris-chalcones and determination of their inhibition profiles against some metabolic enzymes.
Burmaoglu S; Yilmaz AO; Polat MF; Kaya R; Gulcin İ; Algul O
Arch Physiol Biochem; 2021 Apr; 127(2):153-161. PubMed ID: 31172840
[TBL] [Abstract][Full Text] [Related]
12. Investigation of inhibitory properties of some hydrazone compounds on hCA I, hCA II and AChE enzymes.
Kucukoglu K; Gul HI; Taslimi P; Gulcin I; Supuran CT
Bioorg Chem; 2019 May; 86():316-321. PubMed ID: 30743172
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Novel NHC Precursors: Synthesis, Characterization, and Carbonic Anhydrase and Acetylcholinesterase Inhibitory Properties.
Aktaş A; Taslimi P; Gülçin İ; Gök Y
Arch Pharm (Weinheim); 2017 Jun; 350(6):. PubMed ID: 28464340
[TBL] [Abstract][Full Text] [Related]
15. Synthesis of diaryl ethers with acetylcholinesterase, butyrylcholinesterase and carbonic anhydrase inhibitory actions.
Özbey F; Taslimi P; Gülçin İ; Maraş A; Göksu S; Supuran CT
J Enzyme Inhib Med Chem; 2016; 31(sup2):79-85. PubMed ID: 27241224
[TBL] [Abstract][Full Text] [Related]
16. Synthesis, structure elucidation, and in vitro pharmacological evaluation of novel polyfluoro substituted pyrazoline type sulfonamides as multi-target agents for inhibition of acetylcholinesterase and carbonic anhydrase I and II enzymes.
Yamali C; Gul HI; Kazaz C; Levent S; Gulcin I
Bioorg Chem; 2020 Mar; 96():103627. PubMed ID: 32058104
[TBL] [Abstract][Full Text] [Related]
17. Acetylcholinesterase and carbonic anhydrase isoenzymes I and II inhibition profiles of taxifolin.
Gocer H; Topal F; Topal M; Küçük M; Teke D; Gülçin İ; Alwasel SH; Supuran CT
J Enzyme Inhib Med Chem; 2016; 31(3):441-7. PubMed ID: 25893707
[TBL] [Abstract][Full Text] [Related]
18. Schiff bases and their amines: Synthesis and discovery of carbonic anhydrase and acetylcholinesterase enzymes inhibitors.
Yiğit B; Yiğit M; Taslimi P; Gök Y; Gülçin İ
Arch Pharm (Weinheim); 2018 Sep; 351(9):e1800146. PubMed ID: 30033646
[TBL] [Abstract][Full Text] [Related]
19. The first synthesis of 4-phenylbutenone derivative bromophenols including natural products and their inhibition profiles for carbonic anhydrase, acetylcholinesterase and butyrylcholinesterase enzymes.
Bayrak Ç; Taslimi P; Gülçin İ; Menzek A
Bioorg Chem; 2017 Jun; 72():359-366. PubMed ID: 28302311
[TBL] [Abstract][Full Text] [Related]
20. Design, synthesis, characterization, in vitro and in silico evaluation of novel imidazo[2,1-b][1,3,4]thiadiazoles as highly potent acetylcholinesterase and non-classical carbonic anhydrase inhibitors.
Askin S; Tahtaci H; Türkeş C; Demir Y; Ece A; Akalın Çiftçi G; Beydemir Ş
Bioorg Chem; 2021 Aug; 113():105009. PubMed ID: 34052739
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]