Type : Oxime, Pyridinium, Pyridine, Pyridine-aldoxime
Chemical_Nomenclature : 1-hexyl-2-((hydroxyimino)methyl)pyridinium chloride
Canonical SMILES : C1=CC=[N+](C(=C1)C=NC)CCCCCC
InChI : InChI=1S\/C13H21N2\/c1-3-4-5-7-10-15-11-8-6-9-13(15)12-14-2\/h6,8-9,11-12H,3-5,7,10H2,1-2H3\/q+1
InChIKey : DUYPUGMIIVVSQW-UHFFFAOYSA-N
Other name(s) : Compound 5B
Structure : No structure
Families : No family
Title : Click-chemistry-derived oxime library reveals efficient reactivators of nerve agent-inhibited butyrylcholinesterase suitable for pseudo-catalytic bioscavenging - Cadez_2025_Arch.Toxicol__ |
Author(s) : Cadez T , Macek Hrvat N , Sinko G , Kalisiak J , Radic Z , Fokin VV , Sharpless KB , Taylor P , Kovarik Z |
Ref : Archives of Toxicology , : , 2025 |
Abstract : |
PubMedSearch : Cadez_2025_Arch.Toxicol__ |
PubMedID: 40032685 |
Title : Reversal of Tabun Toxicity Enabled by a Triazole-Annulated Oxime Library-Reactivators of Acetylcholinesterase - Kovarik_2019_Chemistry_25_4100 |
Author(s) : Kovarik Z , Kalisiak J , Macek Hrvat N , Katalinic M , Zorbaz T , Zunec S , Green C , Radic Z , Fokin VV , Sharpless KB , Taylor P |
Ref : Chemistry , 25 :4100 , 2019 |
Abstract : |
PubMedSearch : Kovarik_2019_Chemistry_25_4100 |
PubMedID: 30458057 |