Asoxime_chloride

Asoxime chloride
Clinical data
Routes of; administration	Intramuscular injection
ATC code	none;
Legal status
Legal status	Experimental;
Identifiers
	IUPAC name 4-carbamoyl-1-[({2-[(E)-(hydroxyimino)methyl]pyridinium-1-yl}methoxy)methyl]pyridinium dichloride;
CAS Number	34433-31-3 ;
PubChem CID	5484128;
ChemSpider	13004322 ;
UNII	HUV88P6SJS;
ChEMBL	ChEMBL33051 ;
Chemical and physical data
Formula	C14H16Cl2N4O3
Molar mass	359.21 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES C1=CC=[N+](C(=C1)/C=N/O)COC[N+]2=CC=C(C=C2)C(=O)N.[Cl-].[Cl-];
	InChI InChI=1S/C14H14N4O3.2ClH/c15-14(19)12-4-7-17(8-5-12)10-21-11-18-6-2-1-3-13(18)9-16-20;;/h1-9H,10-11H2,(H-,15,19);2*1H ; Key:QELSIJXWEROXOE-UHFFFAOYSA-N ;
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Asoxime chloride

Chemical compound

Asoxime chloride, or more commonly HI-6, is a Hagedorn oxime used in the treatment of organophosphate poisoning.^[1]

Quick Facts Clinical data, Routes ofadministration ...

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[1] [1]
Cochran R, Kalisiak J, Küçükkilinç T, Radic Z, Garcia E, Zhang L, et al. (August 2011). "Oxime-assisted acetylcholinesterase catalytic scavengers of organophosphates that resist aging". The Journal of Biological Chemistry. 286 (34): 29718–24. doi:10.1074/jbc.M111.264739. PMC 3191013. PMID 21730071.

[1]

Clinical data

Routes of administration	Intramuscular injection
ATC code	none
Legal status
Legal status	Experimental
Identifiers
IUPAC name 4-carbamoyl-1-[({2-[(E)-(hydroxyimino)methyl]pyridinium-1-yl}methoxy)methyl]pyridinium dichloride
CAS Number	34433-31-3^N
PubChem CID	5484128
ChemSpider	13004322^Y
UNII	HUV88P6SJS
ChEMBL	ChEMBL33051^Y
Chemical and physical data
Formula	C₁₄H₁₆Cl₂N₄O₃
Molar mass	359.21 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES C1=CC=[N+](C(=C1)/C=N/O)COC[N+]2=CC=C(C=C2)C(=O)N.[Cl-].[Cl-]
InChI InChI=1S/C14H14N4O3.2ClH/c15-14(19)12-4-7-17(8-5-12)10-21-11-18-6-2-1-3-13(18)9-16-20;;/h1-9H,10-11H2,(H-,15,19);2*1H^Y Key:QELSIJXWEROXOE-UHFFFAOYSA-N^Y
^NY (what is this?) (verify)

Asoxime_chloride

References

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