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Reactivator Report for: Triazole-annulated-oxime-14A

General
Type Bispyridinium, Pyridinium, Triazol, Oxime
Chemical_Nomenclature 2-((Hydroxyimino)methyl)-1-((1-(2-(4-((hydroxyimino)methyl)pyridinium-1-yl)ethyl)-1H-1,2,3-triazol-4-yl)methyl)pyridinium hexafluorophosphate
Canonical SMILES C1=CC(=C[N+]([H])=O)N(C=C1)CC2=C[N](N=N2)CCN3C=CC(=C/[N+]([H])=O)C=C3
InChI InChI=1S/C17H17N7O2/c25-18-11-15-4-7-22(8-5-15)9-10-24-14-16(20-21-24)13-23-6-2-1-3-17(23)12-19-26/h1-8,11-12,14H,9-10,13H2/p+2
InChIKey RJEIBECBOLFHLW-UHFFFAOYSA-P
Other name(s)
________________________________________________________________________________________________
MW|353.38
Formula|C17H19N7O2
CAS_number|
PubChem|
UniChem|RJEIBECBOLFHLW-UHFFFAOYSA-P
IUPHAR|
Wikipedia|

Target

References:
Search PubMed for references concerning: Triazole-annulated-oxime-14A
    Title: Reversal of Tabun Toxicity Enabled by a Triazole-Annulated Oxime Library-Reactivators of Acetylcholinesterase
    Kovarik Z, Kalisiak J, Hrvat NM, Katalinic M, Zorbaz T, Zunec S, Green C, Radic Z, Fokin VV and Taylor P <1 more author(s)>
    Ref: Chemistry, 25:4100, 2019 : PubMed

            


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