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104579-02-4

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  • N-[1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-5-methyl-2-oxo-pyrimidin-4-yl]benzamide

    Cas No: 104579-02-4

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  • N-[1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methyl-2-oxopyrimidin-4-yl]benzamide

    Cas No: 104579-02-4

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104579-02-4 Usage

General Description

N4-benzoyl-5-methyldeoxycytidine, also known as tazemetostat, is a synthetic chemical compound that has shown promise in cancer treatment. It is a potent and selective inhibitor of the EZH2 enzyme, which is involved in the regulation of gene expression. Tazemetostat has been found to be effective in inhibiting the growth of cancer cells, particularly in certain types of lymphomas and solid tumors. It is currently being investigated in clinical trials for its potential use in the treatment of various types of cancer, and early results have shown promising anti-tumor activity. Tazemetostat represents a new and potentially valuable tool in the fight against cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 104579-02-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,5,7 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104579-02:
(8*1)+(7*0)+(6*4)+(5*5)+(4*7)+(3*9)+(2*0)+(1*2)=114
114 % 10 = 4
So 104579-02-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H19N3O5/c1-10-8-20(14-7-12(22)13(9-21)25-14)17(24)19-15(10)18-16(23)11-5-3-2-4-6-11/h2-6,8,12-14,21-22H,7,9H2,1H3,(H,18,19,23,24)/t12-,13+,14+/m0/s1

104579-02-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methyl-2-oxopyrimidin-4-yl]benzamide

1.2 Other means of identification

Product number -
Other names Cytidine,N-benzoyl-2'-deoxy-5-methyl

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

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More Details:104579-02-4 SDS

104579-02-4Relevant articles and documents

Unexpected shift to a 4-imino tautomer upon N4-acylation of 5- methylcytosin-1-yl nucleoside analogues

Busson,Kerremans,Van Aerschot,Peeters,Blaton,Herdewijn

, p. 1079 - 1082 (1999)

In contrast with the behaviour of 5-unsubstituted cytosine nucleoside analogues, 5-methylcytosine derivatives show upon N4-benzoylation, commonly used as base protection in oligonucleotide synthesis, a tautomeric change of the base moiety from a 4-amino- into a 4-imino isomer. In the latter form, which is easily diagnosticized by 13C NMR and confirmed by X-ray data, the compounds seem to be hydrolytically less stable.

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