A newly developed oxime K203 is the most effective reactivator of tabun-inhibited acetylcholinesterase-Reference-Cited by-同舟云学术

A newly developed oxime K203 is the most effective reactivator of tabun-inhibited acetylcholinesterase

Published:2018-02-21 Issue:1 Volume:19 Page:
ISSN:2050-6511
Container-title:BMC Pharmacology and Toxicology
language:en
Short-container-title:BMC Pharmacol Toxicol

Author:

Kuca Kamil,Musilek Kamil,Jun Daniel,Zdarova-Karasova Jana,Nepovimova Eugenie,Soukup Ondrej,Hrabinova Martina,Mikler John,Franca Tanos C. C.,Da Cunha Elaine F. F.,De Castro Alexandre A.,Valis Martin,Ramalho Teodorico C.

Funder

Grantová Agentura České Republiky

UHK

UHHK

Brazilian agencies

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology

Link

http://link.springer.com/content/pdf/10.1186/s40360-018-0196-3.pdf

Reference64 articles.

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2. Bajgar J. Organophosphates/nerve agent poisoning: mechanism of action, diagnosis, prophylaxis, and treatment. Adv Clin Chem. 2004;38:151–216.

3. Jokanovic M, Stojiljkovic MP. Current understanding of the application of pyridinium oximes ascholinesterase reactivators in treatment of organophosphate poisoning. Eur J Pharmacol. 2006;553:10–7.

4. Cabal J, Kuca K, Kassa J. Specification of the structure of oximes able to reactivate tabun inhibited acetylcholinesterase. Basic Clin Pharmacol Toxicol. 2004;95(2):81–6.

5. Calic M, Lucic VA, Radic B, Jelic D, Jun D, Kuca K, Kovarik Z. In vitro and in vivo evaluation of pyridinium oximes: mode of interaction with acetylcholinesterase, effect on tabun- and soman-poisoned mice and their cytotoxicity. Toxicol. 2006;219(1-3):85–96.

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