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N-DELTA-2,4-DNP-L-ORNITHINE HYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64821-45-0

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64821-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64821-45-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,8,2 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 64821-45:
(7*6)+(6*4)+(5*8)+(4*2)+(3*1)+(2*4)+(1*5)=130
130 % 10 = 0
So 64821-45-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N4O6.ClH/c12-8(11(16)17)2-1-5-13-9-4-3-7(14(18)19)6-10(9)15(20)21;/h3-4,6,8,13H,1-2,5,12H2,(H,16,17);1H

64821-45-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-5-(2,4-dinitroanilino)pentanoic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names N|A-DNP-L-ornithine hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:64821-45-0 SDS

64821-45-0Downstream Products

64821-45-0Relevant academic research and scientific papers

Nitroaromatic amino acids as inhibitors of neuronal nitric oxide synthase

Cowart, Marion,Kowaluk, Elizabeth A.,Daanen, Jerome F.,Kohlhaas, Kathy L.,Alexander, Karen M.,Wagenaar, Frank L.,Kerwin Jr., James F.

, p. 2636 - 2642 (2007/10/03)

Nitric oxide (NO·) is an important biomodulator of many physiological processes. The inhibition of inappropriate production of NO' by the isoforms of nitric oxide synthase (NOS) has been proposed as a therapeutic approach for the treatment of stroke, inflammation, and other processes. In this study, certain 2-nitroaryl-substituted amino acid analogues were discovered to inhibit NOS. Analogues bearing a 5-methyl substituent on the aromatic ring demonstrated maximal inhibitory potency. For two selected inhibitors, investigation of the kinetics of the enzyme showed the inhibition to be competitive with L-arginine. Additionally, functional NOS inhibition in tissue preparations was demonstrated.

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