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53602-74-7

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53602-74-7 Usage

General Description

The chemical (2S)-2-(acetyl-nitroso-amino)-3-(1H-indol-3-yl)propanoic acid, also known as ANAP, is a compound with a molecular structure consisting of an acetyl-nitroso-amino group attached to a 1H-indol-3-yl propanoic acid backbone. It is an amino acid derivative that can be found in certain food sources, and it has potential implications in the field of pharmaceuticals and medicine due to its unique chemical structure and potential biological activities. Further research and studies are needed to fully understand the properties and potential applications of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 53602-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,0 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53602-74:
(7*5)+(6*3)+(5*6)+(4*0)+(3*2)+(2*7)+(1*4)=107
107 % 10 = 7
So 53602-74-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H13N3O4/c1-8(17)16(15-20)12(13(18)19)6-9-7-14-11-5-3-2-4-10(9)11/h2-5,7,12,14H,6H2,1H3,(H,18,19)/t12-/m0/s1

53602-74-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-acetyl-N1-nitrosotryptophan

1.2 Other means of identification

Product number -
Other names -

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:53602-74-7 SDS

53602-74-7Relevant articles and documents

Comparison of HNO reactivity with tryptophan and cysteine in small peptides

Keceli, Gizem,Moore, Cathy D.,Toscano, John P.

supporting information, p. 3710 - 3713 (2014/12/09)

Recent discoveries of important pharmacological properties have drawn attention to the reactivity of HNO (azanone, nitroxyl) with biologically relevant substrates. Apart from its role in thiol oxidation, HNO has been reported to have nitrosative properties, for example, with tryptophan resulting in N-nitrosotryptophan formation. We have investigated the reactivity of HNO with tryptophan and small peptides containing either tryptophan or both a tryptophan and a cysteine residue. Our results point to the more reactive nature of cysteine towards HNO compared with tryptophan.

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