dc.identifier.uri |
http://dx.doi.org/10.15488/1498 |
|
dc.identifier.uri |
http://www.repo.uni-hannover.de/handle/123456789/1523 |
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dc.contributor.author |
Kuca, Kamil
|
|
dc.contributor.author |
Musilova, Lucie
|
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dc.contributor.author |
Paleček, Jiri
|
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dc.contributor.author |
Cirkva, Vladimir
|
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dc.contributor.author |
Paar, Martin
|
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dc.contributor.author |
Musilek, Kamil
|
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dc.contributor.author |
Hrabinova, Martina
|
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dc.contributor.author |
Pohanka, Miroslav
|
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dc.contributor.author |
Karasova, Jana Zdarova
|
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dc.contributor.author |
Jun, Daniel
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dc.date.accessioned |
2017-05-10T13:25:06Z |
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dc.date.available |
2017-05-10T13:25:06Z |
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dc.date.issued |
2009 |
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dc.identifier.citation |
Kuca, K.; Musilova, L.; Palecek, J.; Cirkva, V.; Paar, M. et al.: Novel bisquaternary oximes - Reactivation of acetylcholinesterase and butyrylcholinesterase inhibited by paraoxon. In: Molecules 14 (2009), Nr. 12, S. 4915-4921. DOI: https://doi.org/10.3390/molecules14124915 |
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dc.description.abstract |
Four novel bisquaternary aldoxime cholinesterase reactivators differing in their chemical structure were prepared. Afterwards, their biological activity was evaluated for their ability to reactivate acetylcholinesterase (AchE; EC 3.1.1.7) and butyryl-cholinesterase (BuChE; EC 3.1.1.8) inhibited by paraoxon. Their reactivation activity was compared with standard reactivators - pralidoxime, obidoxime and HI-6 - which are clinically used at present. As it resulted, none of the prepared compounds surpassed obidoxime, which is considered to be the most potent compound if used for reactivation of AChE inhibited by paraoxon. In case of BuChE reactivation, two compounds (K053 and K068) achieved similar results as obidoxime. |
eng |
dc.description.sponsorship |
Ministry of Defence/FVZ0000604 |
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dc.language.iso |
eng |
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dc.publisher |
Basel : MDPI AG |
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dc.relation.ispartofseries |
Molecules 14 (2009), Nr. 12 |
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dc.rights |
CC BY-NC-SA 3.0 Unported |
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dc.rights.uri |
https://creativecommons.org/licenses/by-nc-sa/3.0/ |
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dc.subject |
Acetylcholinesterase |
eng |
dc.subject |
Butyrylcholinesterase |
eng |
dc.subject |
Nerve agent |
eng |
dc.subject |
Oxime |
eng |
dc.subject |
Pesticide |
eng |
dc.subject |
Reactivator |
eng |
dc.subject |
Scavenger |
eng |
dc.subject |
acetylcholinesterase |
eng |
dc.subject |
cholinesterase |
eng |
dc.subject |
enzyme activator |
eng |
dc.subject |
oxime |
eng |
dc.subject |
paraoxon |
eng |
dc.subject |
article |
eng |
dc.subject |
chemistry |
eng |
dc.subject |
drug effect |
eng |
dc.subject |
metabolism |
eng |
dc.subject |
nuclear magnetic resonance spectroscopy |
eng |
dc.subject |
Acetylcholinesterase |
eng |
dc.subject |
Butyrylcholinesterase |
eng |
dc.subject |
Enzyme Reactivators |
eng |
dc.subject |
Magnetic Resonance Spectroscopy |
eng |
dc.subject |
Oximes |
eng |
dc.subject |
Paraoxon |
eng |
dc.subject.ddc |
540 | Chemie
|
ger |
dc.title |
Novel bisquaternary oximes - Reactivation of acetylcholinesterase and butyrylcholinesterase inhibited by paraoxon |
|
dc.type |
Article |
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dc.type |
Text |
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dc.relation.issn |
1420-3049 |
|
dc.relation.doi |
https://doi.org/10.3390/molecules14124915 |
|
dc.bibliographicCitation.issue |
12 |
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dc.bibliographicCitation.volume |
14 |
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dc.bibliographicCitation.firstPage |
4915 |
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dc.bibliographicCitation.lastPage |
4921 |
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dc.description.version |
publishedVersion |
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tib.accessRights |
frei zug�nglich |
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