402 related articles for article (PubMed ID: 27693733)
1. Pyridoxal oxime derivative potency to reactivate cholinesterases inhibited by organophosphorus compounds.
Bušić V; Katalinić M; Šinko G; Kovarik Z; Gašo-Sokač D
Toxicol Lett; 2016 Nov; 262():114-122. PubMed ID: 27693733
[TBL] [Abstract][Full Text] [Related]
2. Enzyme-kinetic investigation of different sarin analogues reacting with human acetylcholinesterase and butyrylcholinesterase.
Bartling A; Worek F; Szinicz L; Thiermann H
Toxicology; 2007 Apr; 233(1-3):166-72. PubMed ID: 16904809
[TBL] [Abstract][Full Text] [Related]
3. Cholesterol Oxime Olesoxime Assessed as a Potential Ligand of Human Cholinesterases.
Kolić D; Šinko G; Jean L; Chioua M; Dias J; Marco-Contelles J; Kovarik Z
Biomolecules; 2024 May; 14(5):. PubMed ID: 38785995
[TBL] [Abstract][Full Text] [Related]
4. Synthesis, Biological Evaluation, and Docking Studies of Novel Bisquaternary Aldoxime Reactivators on Acetylcholinesterase and Butyrylcholinesterase Inhibited by Paraoxon.
Kuca K; Jun D; Junova L; Musilek K; Hrabinova M; da Silva JAV; Ramalho TC; Valko M; Wu Q; Nepovimova E; França TCC
Molecules; 2018 May; 23(5):. PubMed ID: 29735900
[TBL] [Abstract][Full Text] [Related]
5. Effect of reversible ligands on oxime-induced reactivation of sarin- and cyclosarin-inhibited human acetylcholinesterase.
Scheffel C; Thiermann H; Worek F
Toxicol Lett; 2015 Feb; 232(3):557-65. PubMed ID: 25522658
[TBL] [Abstract][Full Text] [Related]
6. Targeting organophosphorus compounds poisoning by novel quinuclidine-3 oximes: development of butyrylcholinesterase-based bioscavengers.
Zandona A; Katalinić M; Šinko G; Radman Kastelic A; Primožič I; Kovarik Z
Arch Toxicol; 2020 Sep; 94(9):3157-3171. PubMed ID: 32583098
[TBL] [Abstract][Full Text] [Related]
7. Counteracting tabun inhibition by reactivation by pyridinium aldoximes that interact with active center gorge mutants of acetylcholinesterase.
Kovarik Z; Maček Hrvat N; Kalisiak J; Katalinić M; Sit RK; Zorbaz T; Radić Z; Fokin VV; Sharpless KB; Taylor P
Toxicol Appl Pharmacol; 2019 Jun; 372():40-46. PubMed ID: 30978400
[TBL] [Abstract][Full Text] [Related]
8. Potency of several oximes to reactivate human acetylcholinesterase and butyrylcholinesterase inhibited by paraoxon in vitro.
Jun D; Musilova L; Kuca K; Kassa J; Bajgar J
Chem Biol Interact; 2008 Sep; 175(1-3):421-4. PubMed ID: 18617161
[TBL] [Abstract][Full Text] [Related]
9. Suitability of human butyrylcholinesterase as therapeutic marker and pseudo catalytic scavenger in organophosphate poisoning: a kinetic analysis.
Aurbek N; Thiermann H; Eyer F; Eyer P; Worek F
Toxicology; 2009 May; 259(3):133-9. PubMed ID: 19428953
[TBL] [Abstract][Full Text] [Related]
10. Kinetic analysis of interactions of amodiaquine with human cholinesterases and organophosphorus compounds.
Bierwisch A; Wille T; Thiermann H; Worek F
Toxicol Lett; 2016 Mar; 246():49-56. PubMed ID: 26851641
[TBL] [Abstract][Full Text] [Related]
11. Evaluation of high-affinity phenyltetrahydroisoquinoline aldoximes, linked through anti-triazoles, as reactivators of phosphylated cholinesterases.
Maček Hrvat N; Kalisiak J; Šinko G; Radić Z; Sharpless KB; Taylor P; Kovarik Z
Toxicol Lett; 2020 Mar; 321():83-89. PubMed ID: 31863869
[TBL] [Abstract][Full Text] [Related]
12. Can hydroxylamine be a more potent nucleophile for the reactivation of tabun-inhibited AChE than prototype oxime drugs? An answer derived from quantum chemical and steered molecular dynamics studies.
Lo R; Ganguly B
Mol Biosyst; 2014 Jul; 10(9):2368-83. PubMed ID: 24964273
[TBL] [Abstract][Full Text] [Related]
13. Potential of two new oximes in reactivate human acetylcholinesterase and butyrylcholinesterase inhibited by organophosphate compounds: an in vitro study.
Costa MD; Freitas ML; Soares FA; Carratu VS; Brandão R
Toxicol In Vitro; 2011 Dec; 25(8):2120-3. PubMed ID: 21983245
[TBL] [Abstract][Full Text] [Related]
14. 4-Amidophenol Quinone Methide Precursors: Effective and Broad-Scope Nonoxime Reactivators of Organophosphorus-Inhibited Cholinesterases and Resurrectors of Organophosphorus-Aged Acetylcholinesterase.
Lovins AR; Miller KA; Buck AK; Ensey DS; Homoelle RK; Murtha MC; Ward NA; Shanahan LA; Gutti G; Shriwas P; McElroy CA; Callam CS; Hadad CM
ACS Chem Neurosci; 2024 May; 15(9):1813-1827. PubMed ID: 38621296
[TBL] [Abstract][Full Text] [Related]
15. A comparison of the potency of the oxime HLö-7 and currently used oximes (HI-6, pralidoxime, obidoxime) to reactivate nerve agent-inhibited rat brain acetylcholinesterase by in vitro methods.
Kuca K; Cabal J; Kassa J; Jun D; Hrabinová M
Acta Medica (Hradec Kralove); 2005; 48(2):81-6. PubMed ID: 16259317
[TBL] [Abstract][Full Text] [Related]
16. Reactivation of organophosphate-inhibited human AChE by combinations of obidoxime and HI 6 in vitro.
Worek F; Aurbek N; Thiermann H
J Appl Toxicol; 2007; 27(6):582-8. PubMed ID: 17370251
[TBL] [Abstract][Full Text] [Related]
17. Oxime K027: novel low-toxic candidate for the universal reactivator of nerve agent- and pesticide-inhibited acetylcholinesterase.
Kuca K; Musilek K; Jun D; Pohanka M; Ghosh KK; Hrabinova M
J Enzyme Inhib Med Chem; 2010 Aug; 25(4):509-12. PubMed ID: 20192902
[TBL] [Abstract][Full Text] [Related]
18. A common mechanism for resistance to oxime reactivation of acetylcholinesterase inhibited by organophosphorus compounds.
Maxwell DM; Brecht KM; Sweeney RE
Chem Biol Interact; 2013 Mar; 203(1):72-6. PubMed ID: 22982773
[TBL] [Abstract][Full Text] [Related]
19. Interactions between acetylcholinesterase, toxic organophosphorus compounds and a short series of structurally related non-oxime reactivators: Analysis of reactivation and inhibition kinetics in vitro.
Horn G; de Koning MC; van Grol M; Thiermann H; Worek F
Toxicol Lett; 2018 Dec; 299():218-225. PubMed ID: 30312685
[TBL] [Abstract][Full Text] [Related]
20. Potential of Vitamin B6 Dioxime Analogues to Act as Cholinesterase Ligands.
Gašo Sokač D; Zandona A; Roca S; Vikić-Topić D; Lihtar G; Maraković N; Bušić V; Kovarik Z; Katalinić M
Int J Mol Sci; 2022 Nov; 23(21):. PubMed ID: 36362178
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]