37682-82-9

Basic information

• Product Name: L-Ornithine, N5-[iMino(nitroaMino)Methyl]-, ethyl ester, hydrochloride
• Synonyms: L-Ornithine, N5-[iMino(nitroaMino)Methyl]-, ethyl ester, hydrochloride
• CAS NO: 37682-82-9
• Molecular Formula: C₈H₁₇N₅O₄*ClH
• Molecular Weight: 283.71262
• Mol File: 37682-82-9.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: L-Ornithine, N5-[iMino(nitroaMino)Methyl]-, ethyl ester, hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: L-Ornithine, N5-[iMino(nitroaMino)Methyl]-, ethyl ester, hydrochloride(37682-82-9)
• EPA Substance Registry System: L-Ornithine, N5-[iMino(nitroaMino)Methyl]-, ethyl ester, hydrochloride(37682-82-9)

Safety Data

• Hazardous Substances Data: 37682-82-9(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 2149-70-4 N-nitro-L-arginine 

Downstream Products

• 109067-83-6 N^α-(N-benzyloxycarbonyl-glycyl)-N^ω-nitro-L-arginine ethyl ester 
• 75-05-8 acetonitrile 
• 75-09-2 dichloromethane 

Relevant articles and documents

Inhibitory effects of L-arginine derivatives on endothelium-dependent vasorelaxing response to acetylcholine of the rat aorta

Nω-nitro-L-arginine alkyl esters (A-1-A-B) and L-arginine alkyl esters (E-1-E-B) were synthesized, and the vasorelaxing effects of acetylcholine were studied in the absence or presence of these compounds in rat aortic rings with intact endothelium that was precontracted with phenylephrine. These compounds revealed that the nitro group is an essential inhibiting group of these inhibitors, and that hydrophobic functional groups can fine-tune the binding effects. Among them, A-3 is the most potent inhibitor.