141968-19-6

Basic information

• Product Name: D-NAME
• Synonyms: D-NAME;NOMEGA-NITRO-D-ARGININE METHYL ESTER;NG-Nitro-D-arginine methyl;ω-Nitro-D-arginine methyl;ω-Nitro-D-arginine methyl ester
• CAS NO: 141968-19-6
• Molecular Formula: C₇H₁₅N₅O₄
• Molecular Weight: 233.23
• Mol File: 141968-19-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 383.5°Cat760mmHg
• Flash Point: 185.8°C
• Appearance: /
• Density: 1.48g/cm³
• Vapor Pressure: 4.37E-06mmHg at 25°C
• Refractive Index: 1.584
• CAS DataBase Reference: D-NAME(CAS DataBase Reference)
• NIST Chemistry Reference: D-NAME(141968-19-6)
• EPA Substance Registry System: D-NAME(141968-19-6)

Safety Data

• Hazardous Substances Data: 141968-19-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H15N5O4/c1-16-6(13)5(8)3-2-4-10-7(9)11-12(14)15/h5H,2-4,8H2,1H3,(H3,9,10,11)/t5-/m1/s1

Upstream product

• 627-75-8 D-arginine hydrochloride 
• 67-56-1 methanol 
• 66036-77-9 Nω-nitro-D-arginine 
• 112208-06-7 N^α-(tert-butoxycarbonyl)-N^G-nitro-L-arginine methyl ester 
• 2188-18-3 Boc-Arg(NO₂)-OH 
• 1119-34-2 L-arginine hydrochloride 
• 2149-70-4 N-nitro-L-arginine 

Downstream Products

• 106386-19-0 N^α-(N²,N⁶-bis-benzyloxycarbonyl-L-lysyl)-N^ω-nitro-L-arginine methyl ester 
• 66345-00-4 C₁₈H₂₆N₆O₇ 
• 23734-44-3 Cbo-L-Val-nitro-L-Arg-methylester 
• 106655-93-0 -(nitro-L-arginin-methylester) 
• 81666-53-7 Z-glycyl-N^G-nitro-L-arginine methyl ester 
• 26061-11-0 Boc-L-Phe-L-Arg^NO₂-OMe 
• 16876-12-3 N-Benzyloxycarbonyl-(α-tert.butyl-γ-Glu)-(ω-N-nitro-Arg)-methylester 
• 5619-24-9 C₂₃H₃₄N₆O₉ 
• 2785-17-3 N^α-(N²-benzyloxycarbonyl-L-asparaginyl)-N^ω-nitro-L-arginine methyl ester 
• 406952-80-5 2-(S)-(2-(R)-tert-butoxycarbonylamino-3-phenyl-propionylamino)-5-nitroguanidino-pentanoic acid methyl ester 
• 1000072-69-4 methyl (2S)-5-(2-nitroguanidino)-2-((3-phenylaziridin-2-yl)methylamino)pentanoate 
• 1186506-68-2 C₃₄H₄₇N₇O₉ 
• 64181-07-3 3β-hydroxy-lup-20(29)-en-30-al 
• 1207974-55-7 (S)-5-N(G)-nitro-guanidino-2-{[3-(4-nitro-benzenesulfonylamino)thiophene-2-carbonyl]amino}pentanoic acid methyl ester 

Relevant articles and documents

A class of novel Schiff's bases: Synthesis, therapeutic action for chronic pain, anti-inflammation and 3D QSAR analysis

To discover analgesics for treating chronic pain 17 novel Schiff's bases, N,N′-(Z-allylidene-1,3-diyl)bisamino acid methyl esters were prepared from 1,1,3,3,-tetramethoxypropane and amino acid methyl esters. On tail-flick mouse model 20 μmol/kg of these Schiff's bases were orally administered, the analgesic action started 30 min after administration, reached the maximum 120 min after administration, and at 180 min this action was still observed. On a xylene-induced ear edema mouse model 20 μmol/kg of these Schiff's bases exhibited desirable anti-inflammation. Thus the present Schiff's bases are able to treat chronic pain from inflammation. The effect of the side chains of the amino acid residues of these Schiff's bases on the analgesic activity was explained with 3D QSAR.