Desnitro-imidacloprid

Desnitro-imidacloprid
Names
	IUPAC name 1-(6-Chloro-pyridin-3-yl)methyl-2-iminoimidazolidine
Identifiers
CAS Number	115970-17-7;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL309804;
ChemSpider	8306043;
PubChem CID	10130527;
CompTox Dashboard (EPA)	DTXSID90436011;
	InChI InChI=1S/C9H11ClN4/c10-8-2-1-7(5-13-8)6-14-4-3-12-9(14)11/h1-2,5H,3-4,6H2,(H2,11,12) Key: UEQZFAGVRGWPDK-UHFFFAOYSA-N;
	SMILES C1CN(C(=N1)N)CC2=CN=C(C=C2)Cl;
Properties
Chemical formula	C9H11ClN4
Molar mass	210.67 g·mol−1
Appearance	Colorless crystals
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Desnitro-imidacloprid is a metabolite of the insecticide imidacloprid, a very common insecticide and the most important member of the class of insecticides called neonicotinoids, the only significant new class of insecticides to be developed between 1970 and 2000.[1] While imidacloprid has proved highly selective against insects, the desnitro- version is highly toxic to mammals, due to its agonist action at the alpha4beta2 nicotinic acetylcholine receptor (nAChR) in the mammalian brain, at least as demonstrated in experiments involving mice.[1]

References

M. Towizawa; J.E. Casida (1 November 2002). "Desnitro-imidacloprid activates the extracellular signal-regulated kinase cascade via the nicotinic receptor and intracellular calcium mobilization in N1E-115 cells". Toxicol Appl Pharmacol. 184 (3): 180–186.

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[ref1-1] M. Towizawa; J.E. Casida (1 November 2002). "Desnitro-imidacloprid activates the extracellular signal-regulated kinase cascade via the nicotinic receptor and intracellular calcium mobilization in N1E-115 cells". Toxicol Appl Pharmacol. 184 (3): 180–186.