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52278-77-0

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52278-77-0 Usage

Uses

5-Hydroxy-2’-deoxycytidine have been used as a substrate for uracil DNA N-glycosylase and has been used to study the oxidation of DNA due to exposure to reactive oxygen species.

Check Digit Verification of cas no

The CAS Registry Mumber 52278-77-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,7 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52278-77:
(7*5)+(6*2)+(5*2)+(4*7)+(3*8)+(2*7)+(1*7)=130
130 % 10 = 0
So 52278-77-0 is a valid CAS Registry Number.

52278-77-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-HYDROXY-2'-DEOXYCYTIDINE

1.2 Other means of identification

Product number -
Other names 5-Hydroxy-2`-deoxycytidine

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:52278-77-0 SDS

52278-77-0Upstream product

52278-77-0Relevant articles and documents

Reaction of 2′-deoxycytidine with peroxynitrite in the presence of ammonium bromide

Suzuki, Toshinori,Ida, Kazuya,Uchibe, Shinya,Inukai, Michiyo

, p. 5164 - 5170 (2008/12/20)

Peroxynitrite, a reactive nitrogen species generated from nitric oxide and superoxide anion radical, is an endogenous potential risk factor for human cancer. When 2′-deoxycytidine was incubated with peroxynitrite at neutral pH and 37 °C, the reaction was greatly enhanced by the addition of ammonium bromide. Both ammonium ion and bromide ion were required to exert the enhancing effect. In addition to ammonium ion, methylamine and dimethylamine exerted the enhancing effect in the presence of bromide ion. Two major products were identified as 5-hydroxy-2′-deoxycytidine and 5-bromo-2′-deoxycytidine. Hypochlorite solution and bromine water reacted with 2′-deoxycytidine generating 5-hydroxy-2′-deoxycytidine and 5-bromo-2′-deoxycytidine in the presence of ammonium bromide with the yields similar to those of the reaction of peroxynitrite with ammonium bromide. Fenton reaction of 2′-deoxycytidine was suppressed by the addition of ammonium bromide. Nitrogen dioxide gas did not react with 2′-deoxycytidine in the presence or the absence of ammonium bromide. These results suggest that in the presence of ammonium ion or amines, bromide ion interacts with peroxynitrous acid, which is a protonated form of peroxynitrite, but not with hydroxyl radical or nitrogen dioxide generated by homolysis of peroxynitrous acid, to form hypobromous acid. In the presence of ammonium ion or amines, bromide ion may play a role in enhancing the genotoxic effects of peroxynitrite in humans.

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