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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 35857901)

  • 1. 2-Amino thiazole derivatives as inhibitors of some metabolic enzymes: An in vitro and in silico study.
    Korkmaz IN
    Biotechnol Appl Biochem; 2023 Apr; 70(2):659-669. PubMed ID: 35857901
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Synthesis and biological evaluation of aminomethyl and alkoxymethyl derivatives as carbonic anhydrase, acetylcholinesterase and butyrylcholinesterase inhibitors.
    Gulçin İ; Abbasova M; Taslimi P; Huyut Z; Safarova L; Sujayev A; Farzaliyev V; Beydemir Ş; Alwasel SH; Supuran CT
    J Enzyme Inhib Med Chem; 2017 Dec; 32(1):1174-1182. PubMed ID: 28891347
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Pyrimidines: Molecular docking and inhibition studies on carbonic anhydrase and cholinesterases.
    Duran HE
    Biotechnol Appl Biochem; 2023 Feb; 70(1):68-82. PubMed ID: 35112394
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Synthesis, characterization, evaluation of metabolic enzyme inhibitors and in silico studies of thymol based 2-amino thiol and sulfonic acid compounds.
    Bora RE; Genc Bilgicli H; Üç EM; Alagöz MA; Zengin M; Gulcin İ
    Chem Biol Interact; 2022 Oct; 366():110134. PubMed ID: 36057360
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Synthesis, Characterization and Cholinesterase Inhibition Studies of New Arylidene Aminothiazolylethanone Derivatives.
    Channar PA; Shah MS; Saeed A; Khan SU; Larik FA; Shabir G; Iqbal J
    Med Chem; 2017; 13(7):648-653. PubMed ID: 28266279
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synthesis and molecular docking simulation of new benzimidazole-thiazole hybrids as cholinesterase inhibitors.
    Dawood DH; Srour AM; Omar MA; Farghaly TA; El-Shiekh RA
    Arch Pharm (Weinheim); 2024 Jan; 357(1):e2300201. PubMed ID: 37937360
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Design and Synthesis of Pyrazole Carboxamide Derivatives as Selective Cholinesterase and Carbonic Anhydrase Inhibitors: Molecular Docking and Biological Evaluation.
    Durgun M; Akocak S; Lolak N; Topal F; Koçyiğit ÜM; Türkeş C; Işık M; Beydemir Ş
    Chem Biodivers; 2024 Feb; 21(2):e202301824. PubMed ID: 38149720
    [TBL] [Abstract][Full Text] [Related]  

  • 8. In silico, theoretical biointerface analysis and in vitro kinetic analysis of amine compounds interaction with acetylcholinesterase and butyrylcholinesterase.
    Kandasamy S; Loganathan C; Sakayanathan P; Karthikeyan S; Stephen AD; Marimuthu DK; Ravichandran S; Sivalingam V; Thayumanavan P
    Int J Biol Macromol; 2021 Aug; 185():750-760. PubMed ID: 34216669
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Synthesis of novel bis-sulfone derivatives and their inhibition properties on some metabolic enzymes including carbonic anhydrase, acetylcholinesterase, and butyrylcholinesterase.
    Biçer A; Kaya R; Anıl B; Turgut Cin G; Gülcin İ; Gültekin MS
    J Biochem Mol Toxicol; 2019 Nov; 33(11):e22401. PubMed ID: 31581370
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Exploring enzyme inhibition profiles of novel halogenated chalcone derivatives on some metabolic enzymes: Synthesis, characterization and molecular modeling studies.
    Anil DA; Polat MF; Saglamtas R; Tarikogullari AH; Alagoz MA; Gulcin I; Algul O; Burmaoglu S
    Comput Biol Chem; 2022 Oct; 100():107748. PubMed ID: 35917597
    [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. 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]  

  • 13. Design and discovery of Novel Thiazole acetamide derivatives as anticholinesterase agent for possible role in the management of Alzheimer's.
    Sun ZQ; Tu LX; Zhuo FJ; Liu SX
    Bioorg Med Chem Lett; 2016 Feb; 26(3):747-750. PubMed ID: 26783181
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel quinazolin-sulfonamid derivatives: synthesis, characterization, biological evaluation, and molecular docking studies.
    Sepehri N; Mohammadi-Khanaposhtani M; Asemanipoor N; Hosseini S; Biglar M; Larijani B; Mahdavi M; Hamedifar H; Taslimi P; Sadeghian N; Norizadehtazehkand M; Gulcin I
    J Biomol Struct Dyn; 2022 May; 40(8):3359-3370. PubMed ID: 33222620
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Synthesis and in vitro evaluation of new derivatives of 2-substituted-6-fluorobenzo[d]thiazoles as cholinesterase inhibitors.
    Imramovský A; Pejchal V; Štěpánková Š; Vorčáková K; Jampílek J; Vančo J; Šimůnek P; Královec K; Brůčková L; Mandíková J; Trejtnar F
    Bioorg Med Chem; 2013 Apr; 21(7):1735-48. PubMed ID: 23462716
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel sulfamate derivatives of menthol: Synthesis, characterization, and cholinesterases and carbonic anhydrase enzymes inhibition properties.
    Daryadel S; Atmaca U; Taslimi P; Gülçin İ; Çelik M
    Arch Pharm (Weinheim); 2018 Nov; 351(11):e1800209. PubMed ID: 30255953
    [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]
    of 9.