Drug General Information
Drug ID	D0S7MJ
Former ID	DNC009024
Drug Name	(S)-N-(1-phenylethyl)acetimidamide hydrobromide
Drug Type	Small molecular drug
Indication	Discovery agent		Investigative	[531201]
Structure		Download 2D MOL 3D MOL
Formula	C10H15BrN2
Canonical SMILES	CC(C1=CC=CC=C1)N=C(C)N.Br
InChI	1S/C10H14N2.BrH/c1-8(12-9(2)11)10-6-4-3-5-7-10;/h3-8H,1-2H3,(H2,11,12);1H/t8-;/m0./s1
InChIKey	SXSWEEJYFGUAON-QRPNPIFTSA-N
PubChem Compound ID	25231669
Target and Pathway
Target(s)	Nitric oxide synthase, inducible	Target Info	Inhibitor	[531201]
BioCyc Pathway	Citrulline-nitric oxide cycle
KEGG Pathway	Arginine biosynthesis
	Arginine and proline metabolism
	Metabolic pathways
	Calcium signaling pathway
	HIF-1 signaling pathway
	Peroxisome
	Salmonella infection
	Pertussis
	Leishmaniasis
	Chagas disease (American trypanosomiasis)
	Toxoplasmosis
	Amoebiasis
	Tuberculosis
	Pathways in cancer
	Small cell lung cancer
NetPath Pathway	IL1 Signaling Pathway
	IL2 Signaling Pathway
Pathway Interaction Database	IL12-mediated signaling events
	Alpha9 beta1 integrin signaling events
	ATF-2 transcription factor network
	IL23-mediated signaling events
	Signaling mediated by p38-alpha and p38-beta
	HIF-1-alpha transcription factor network
Reactome	ROS production in response to bacteria
	Nitric oxide stimulates guanylate cyclase
WikiPathways	Type II interferon signaling (IFNG)
	Spinal Cord Injury
	AGE/RAGE pathway
	Effects of Nitric Oxide
References
Ref 531201	Bioorg Med Chem Lett. 2010 Nov 15;20(22):6495-9. Epub 2010 Sep 17.N-Substituted acetamidines and 2-methylimidazole derivatives as selective inhibitors of neuronal nitric oxide synthase.
Ref 531201	Bioorg Med Chem Lett. 2010 Nov 15;20(22):6495-9. Epub 2010 Sep 17.N-Substituted acetamidines and 2-methylimidazole derivatives as selective inhibitors of neuronal nitric oxide synthase.

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