Reactivator Report for: PAM

General

Type		Oxime
Chemical_Nomenclature		(2E)-2-(nitrosomethylidene)-1H-pyridine
Canonical SMILES		C1=CC(=CN=O)NC=C1
InChI		InChI=1S/C6H6N2O/c9-8-5-6-3-1-2-4-7-6/h1-5,9H/b8-5+
InChIKey		MTFJSAGADRTKCI-VMPITWQZSA-N VRGKDCRTYBCJTA-WAYWQWQTSA-N
Other name(s)		CHEMBL77510 ; SCHEMBL103202 ; ZINC04758521 ; (2Z)-2-(nitrosomethylidene)-1H-pyridine ; 2-Pyridinecarboxaldehyde oxime ; syn-2-Pyridinealdoxime ; 2-Pyridinecarbaldehyde oxime ; 2-Pyridinealdoxime ; Pyridine-2-aldoxime ; Picolinaldoxime ; 2-Pyridylaldoxime ; Pyridine 2-aldoxime ; Pyridine-2-aldoximate ; Picolinaldehyde, oxime ; (E)-Picolinaldehyde oxime ; 2-Pyridinecarboxaldoxime ; UNII-QD6R9FJW69 ; 2-pyridine aldoxime ; Picolinaldehyde oxime

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MW	\|	122.13
Formula	\|	C6H6N2O
CAS_number	\|	1193-96-0
PubChem	\|	5371221
UniChem	\|	MTFJSAGADRTKCI-VMPITWQZSA-N, VRGKDCRTYBCJTA-WAYWQWQTSA-N
IUPHAR	\|
Wikipedia	\|	Pralidoxime

Target

References:

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Send your questions or comments to :Mail to: Nicolas Lenfant, Thierry Hotelier, Yves Bourne, Pascale Marchot and Arnaud Chatonnet.Please cite: Lenfant 2013 Nucleic.Acids.Res. or Marchot Chatonnet 2012 Prot.Pept Lett.

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