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123994-81-0

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123994-81-0 Usage

Class

Purine analogs

Type

Synthetic nucleoside

Activities

Antineoplastic and antiviral

Mechanism of action

Inhibits DNA methylation, leading to re-expression of silenced tumor suppressor genes and inhibition of cancer cell growth

Potential applications

Treatment of solid tumors and hematological malignancies, development of antiviral drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 123994-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,9,9 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 123994-81:
(8*1)+(7*2)+(6*3)+(5*9)+(4*9)+(3*4)+(2*8)+(1*1)=150
150 % 10 = 0
So 123994-81-0 is a valid CAS Registry Number.

123994-81-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4-dichloroanilino)-3,7-dihydropurin-6-one

1.2 Other means of identification

Product number -
Other names 6H-Purin-6-one,2-[(3,4-dichlorophenyl)amino]-1,9-dihydro

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:123994-81-0 SDS

123994-81-0Downstream Products

123994-81-0Relevant articles and documents

Haloanilino derivatives of pyrimidines, purines, and purine nucleoside analogs: Synthesis and activity against human cytomegalovirus

Medveczky,Yang,Gambino,Medveczky,Wright

, p. 1811 - 1819 (2007/10/02)

2-Anilinopurines and 6-anilinopyrimidines bearing 3,4- or 3,5-dichloro substituents in the anilino ring inhibited virus-specific DNA synthesis by human cytomegalovirus (HCMV)-infected human embryonic lung (HEL) cells in culture. In general, active compounds had moderate to low selectivity for viral vs host cell DNA synthesis. Nucleoside and acyclonucleoside analogs of 2-(3,5-dichloroanilino)purines inhibited both HCMV and cellular DNA synthesis at similar concentrations. 2-Amino-4-chloro-6-(3,5- dichloroanilino)pyrimidine and several related compounds inhibited HCMV growth in yield reduction assays at concentrations that were nontoxic to HEL cells.

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