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5-methyl-7-pentofuranosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine, also known as 5-methylcytosine, is a chemical compound derived from cytosine, a pyrimidine nucleobase found in DNA and RNA. 5-methyl-7-pentofuranosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine is formed when a methyl group (-CH3) is added to the cytosine molecule at the 5th carbon position. 5-methylcytosine plays a crucial role in epigenetics, as it is involved in the regulation of gene expression without altering the DNA sequence itself. It is commonly found in CpG dinucleotides, where a cytosine nucleotide is followed by a guanine nucleotide in the DNA sequence. The methylation of cytosine at this position can lead to gene silencing, which is essential for various biological processes, including embryonic development, genomic imprinting, and X-chromosome inactivation. The study of 5-methylcytosine and its role in gene regulation has significant implications for understanding the molecular basis of various diseases and developing potential therapeutic strategies.

64609-53-6

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64609-53-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64609-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,6,0 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 64609-53:
(7*6)+(6*4)+(5*6)+(4*0)+(3*9)+(2*5)+(1*3)=136
136 % 10 = 6
So 64609-53-6 is a valid CAS Registry Number.

64609-53-6SDS

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 2-(4-amino-5-methylpyrrolo[2,3-d]pyrimidin-7-yl)-5-(hydroxymethyl)oxolane-3,4-diol

1.2 Other means of identification

Product number -
Other names 7-methyl-7-deaza-adenosine

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:64609-53-6 SDS

64609-53-6Downstream Products

64609-53-6Relevant academic research and scientific papers

Enzymatic synthesis of base-modified RNA by T7 RNA polymerase. A systematic study and comparison of 5-substituted pyrimidine and 7-substituted 7-deazapurine nucleoside triphosphates as substrates

Milisavljevi?, Nemanja,Perlíková, Pavla,Pohl, Radek,Hocek, Michal

supporting information, p. 5800 - 5807 (2018/08/22)

We synthesized a small library of eighteen 5-substituted pyrimidine or 7-substituted 7-deazapurine nucleoside triphosphates bearing methyl, ethynyl, phenyl, benzofuryl or dibenzofuryl groups through cross-coupling reactions of nucleosides followed by triphosphorylation or through direct cross-coupling reactions of halogenated nucleoside triphosphates. We systematically studied the influence of the modification on the efficiency of T7 RNA polymerase catalyzed synthesis of modified RNA and found that modified ATP, UTP and CTP analogues bearing smaller modifications were good substrates and building blocks for the RNA synthesis even in difficult sequences incorporating multiple modified nucleotides. Bulky dibenzofuryl derivatives of ATP and GTP were not substrates for the RNA polymerase. In the case of modified GTP analogues, a modified procedure using a special promoter and GMP as initiator needed to be used to obtain efficient RNA synthesis. The T7 RNA polymerase synthesis of modified RNA can be very efficiently used for synthesis of modified RNA but the method has constraints in the sequence of the first three nucleotides of the transcript, which must contain a non-modified G in the +1 position.

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