139 related articles for article (PubMed ID: 32851915)
21. Synephrine and phenylephrine act as α-amylase, α-glycosidase, acetylcholinesterase, butyrylcholinesterase, and carbonic anhydrase enzymes inhibitors.
Taslimi P; Akıncıoglu H; Gülçin İ
J Biochem Mol Toxicol; 2017 Nov; 31(11):. PubMed ID: 28800181
[TBL] [Abstract][Full Text] [Related]
22. The impact of some natural phenolic compounds on carbonic anhydrase, acetylcholinesterase, butyrylcholinesterase, and α-glycosidase enzymes: An antidiabetic, anticholinergic, and antiepileptic study.
Taslimi P; Caglayan C; Gulcin İ
J Biochem Mol Toxicol; 2017 Dec; 31(12):. PubMed ID: 28902458
[TBL] [Abstract][Full Text] [Related]
23. Novel functionally substituted esters based on sodium diethyldithiocarbamate derivatives: Synthesis, characterization, biological activity and molecular docking studies.
Karimov A; Orujova A; Taslimi P; Sadeghian N; Mammadov B; Karaman HS; Farzaliyev V; Sujayev A; Tas R; Alwasel S; Gulçin İ
Bioorg Chem; 2020 Jun; 99():103762. PubMed ID: 32224335
[TBL] [Abstract][Full Text] [Related]
24. Synthesis, molecular docking, and biological activities of new cyanopyridine derivatives containing phenylurea.
Gezegen H; Gürdere MB; Dinçer A; Özbek O; Koçyiğit ÜM; Taslimi P; Tüzün B; Budak Y; Ceylan M
Arch Pharm (Weinheim); 2021 Apr; 354(4):e2000334. PubMed ID: 33300644
[TBL] [Abstract][Full Text] [Related]
25. Design, synthesis, and evaluation of novel bistrifluoromethyl-based hydrazones as dual inhibitors of acetylcholinesterase and carbonic anhydrase enzymes for Alzheimer's disease.
Dincel ED; Başoğlu-Ünal F; Kuran ED; Kayra T; Aydın N; Kanber E; Gülçin İ; Ulusoy-Güzeldemirci N
Chem Biol Drug Des; 2024 Feb; 103(2):e14482. PubMed ID: 38378259
[TBL] [Abstract][Full Text] [Related]
26. 1,2,3-Triazole substituted phthalocyanine metal complexes as potential inhibitors for anticholinesterase and antidiabetic enzymes with molecular docking studies.
Koçyiğit ÜM; Taslimi P; Tüzün B; Yakan H; Muğlu H; Güzel E
J Biomol Struct Dyn; 2022 Jul; 40(10):4429-4439. PubMed ID: 33292060
[TBL] [Abstract][Full Text] [Related]
27. Synthesis, characterization, and SAR of arylated indenoquinoline-based cholinesterase and carbonic anhydrase inhibitors.
Ekiz M; Tutar A; Ökten S; Bütün B; Koçyiğit ÜM; Taslimi P; Topçu G
Arch Pharm (Weinheim); 2018 Sep; 351(9):e1800167. PubMed ID: 30079554
[TBL] [Abstract][Full Text] [Related]
28. Novel 2-methylimidazolium salts: Synthesis, characterization, molecular docking, and carbonic anhydrase and acetylcholinesterase inhibitory properties.
Bal S; Kaya R; Gök Y; Taslimi P; Aktaş A; Karaman M; Gülçin İ
Bioorg Chem; 2020 Jan; 94():103468. PubMed ID: 31791684
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. meta-Cyanobenzyl substituted benzimidazolium salts: Synthesis, characterization, crystal structure and carbonic anhydrase, α-glycosidase, butyrylcholinesterase, and acetylcholinesterase inhibitory properties.
Türker F; Barut Celepci D; Aktaş A; Taslimi P; Gök Y; Aygün M; Gülçin İ
Arch Pharm (Weinheim); 2018 Jul; 351(7):e1800029. PubMed ID: 29963738
[TBL] [Abstract][Full Text] [Related]
31. Novel benzoic acid derivatives: Synthesis and biological evaluation as multitarget acetylcholinesterase and carbonic anhydrase inhibitors.
Kalaycı M; Türkeş C; Arslan M; Demir Y; Beydemir Ş
Arch Pharm (Weinheim); 2021 Mar; 354(3):e2000282. PubMed ID: 33155700
[TBL] [Abstract][Full Text] [Related]
32. Synthesis and in silico studies of triazene-substituted sulfamerazine derivatives as acetylcholinesterase and carbonic anhydrases inhibitors.
Bilginer S; Gul HI; Anil B; Demir Y; Gulcin I
Arch Pharm (Weinheim); 2021 Jan; 354(1):e2000243. PubMed ID: 32984993
[TBL] [Abstract][Full Text] [Related]
33. The synthesis of novel sulfamides derived from β-benzylphenethylamines as acetylcholinesterase, butyrylcholinesterase and carbonic anhydrase enzymes inhibitors.
Akıncıoğlu A; Kocaman E; Akıncıoğlu H; Salmas RE; Durdagi S; Gülçin İ; Supuran CT; Göksu S
Bioorg Chem; 2017 Oct; 74():238-250. PubMed ID: 28866249
[TBL] [Abstract][Full Text] [Related]
34. Phthalocyanine complexes with (4-isopropylbenzyl)oxy substituents: preparation and evaluation of anti-carbonic anhydrase, anticholinesterase enzymes and molecular docking studies.
Güzel E; Koçyiğit ÜM; Taslimi P; Gülçin İ; Erkan S; Nebioğlu M; Arslan BS; Şişman İ
J Biomol Struct Dyn; 2022 Feb; 40(2):733-741. PubMed ID: 32954954
[TBL] [Abstract][Full Text] [Related]
35. Synthesis of β-amino acid derivatives and their inhibitory profiles against some metabolic enzymes.
Atmaca U; Daryadel S; Taslimi P; Çelik M; Gülçin İ
Arch Pharm (Weinheim); 2019 Dec; 352(12):e1900200. PubMed ID: 31544276
[TBL] [Abstract][Full Text] [Related]
36. Antioxidant Activity, Acetylcholinesterase, and Carbonic Anhydrase Inhibitory Properties of Novel Ureas Derived from Phenethylamines.
Aksu K; Özgeriş B; Taslimi P; Naderi A; Gülçin İ; Göksu S
Arch Pharm (Weinheim); 2016 Dec; 349(12):944-954. PubMed ID: 27862205
[TBL] [Abstract][Full Text] [Related]
37. Synthesis and discovery of potent carbonic anhydrase, acetylcholinesterase, butyrylcholinesterase, and α-glycosidase enzymes inhibitors: The novel N,N'-bis-cyanomethylamine and alkoxymethylamine derivatives.
Taslimi P; Caglayan C; Farzaliyev V; Nabiyev O; Sujayev A; Turkan F; Kaya R; Gulçin İ
J Biochem Mol Toxicol; 2018 Apr; 32(4):e22042. PubMed ID: 29457667
[TBL] [Abstract][Full Text] [Related]
38. Synthesis, biological evaluation and in silico studies of novel N-substituted phthalazine sulfonamide compounds as potent carbonic anhydrase and acetylcholinesterase inhibitors.
Türkeş C; Arslan M; Demir Y; Çoçaj L; Rifati Nixha A; Beydemir Ş
Bioorg Chem; 2019 Aug; 89():103004. PubMed ID: 31129502
[TBL] [Abstract][Full Text] [Related]
39. Synthesis of nitrogen, phosphorus, selenium and sulfur-containing heterocyclic compounds - Determination of their carbonic anhydrase, acetylcholinesterase, butyrylcholinesterase and α-glycosidase inhibition properties.
Gülçin İ; Trofimov B; Kaya R; Taslimi P; Sobenina L; Schmidt E; Petrova O; Malysheva S; Gusarova N; Farzaliyev V; Sujayev A; Alwasel S; Supuran CT
Bioorg Chem; 2020 Oct; 103():104171. PubMed ID: 32891857
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
