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Reactivator Report for: 6-Alkyl-3-Fluoro-2-pyridinaldoxime-12d

6-Alkyl-3-Fluoro-2-pyridinaldoxime-12d	Type	Pyridine
		Oxime
	Chemical_Nomenclature	N-[[3-fluoro-6-(2-pyridin-3-ylethyl)pyridin-2-yl]methylidene]hydroxylamine
	Formula	C13H12FN3O
	MW	245.25
	Paper	Yerri_2020_Chemistry_26_15035
	Comment	compound 12d greater affinity and higher reactivation efficiency(kr2=83 mm-1.min-1) than 2-PAM and HI-6.Compound 12d seven times more efficient in the reactivation of sarin-inhibited AChE compared with 2-PAM,and six times more efficient than HI-6. Compound12d completely inefficient in reactivating tabun-inhibited hAChE
	CID	138559949
	InChIKey	CKUUWPBCPYJLIA-UHFFFAOYSA-N
	CanonicalSMILES	C1=CC(=CN=C1)CCC2=NC(=C(C=C2)F)C=NO
	InChI	InChI=1S/C13H12FN3O/c14-12-6-5-11(17-13(12)9-16-18)4-3-10-2-1-7-15-8-10/h1-2,5-9,18H,3-4H2