CAS 443-72-1
:N6-Methyladenine
Description:
N6-Methyladenine is a derivative of adenine, a purine nucleobase that plays a crucial role in various biological processes, including DNA and RNA synthesis. This compound is characterized by the presence of a methyl group attached to the nitrogen atom at the sixth position of the adenine ring structure. It is a white to off-white solid that is soluble in polar solvents such as water and methanol. N6-Methyladenine is known to participate in various biochemical pathways and has been studied for its potential roles in gene regulation and cellular signaling. Its structural modification can influence the stability and function of nucleic acids, making it a subject of interest in molecular biology and biochemistry. Additionally, N6-Methyladenine has been implicated in epigenetic regulation, as it can affect the expression of genes by modifying chromatin structure. Overall, this compound serves as an important tool for researchers exploring the complexities of genetic regulation and cellular processes.
Formula:C6H7N5
InChI:InChI=1S/C6H7N5/c1-7-5-4-6(10-2-8-4)11-3-9-5/h2-3H,1H3,(H2,7,8,9,10,11)
InChI key:InChIKey=CKOMXBHMKXXTNW-UHFFFAOYSA-N
SMILES:N(C)C1=C2C(N=CN2)=NC=N1
Synonyms:- 1H-Purin-6-amine, N-methyl-
- 6-(N-Methylamino)purine
- 6-Map
- 6-Methyladenine
- 6-Methylaminopurine
- 6-Mono(methylamino)purine
- 6-N-Methyladenine
- 9H-Purin-6-amine, N-methyl-
- Adenine, N-methyl-
- Methyl(Purin-6-Yl)Amine
- N-Methyl-6-aminopurine
- N-Methyl-9H-purin-6-amine
- N-methyl-5H-purin-6-amine
- N-methyl-7H-purin-6-amine
- N6-Methylademine
- N6-Methyladenine
- N<sup>6</sup>-Methyladenine
- N<sup>6</sup>-Methylaminopurine
- N<sup>6</sup>-Monomethyladenine
- See more synonyms
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Found 10 products.
1H-Purin-6-amine, N-methyl-
CAS:Formula:C6H7N5Purity:95%Color and Shape:SolidMolecular weight:149.1533N6-Methyladenine
CAS:<p>N6-Methyladenine (6-(Methylamino)Purine) is a modified purine commonly found in genomes of prokaryotes, protists, and plants.</p>Formula:C6H7N5Purity:99.78%Color and Shape:SolidMolecular weight:149.15N-Methyl-7H-purin-6-amine
CAS:Formula:C6H7N5Purity:>98.0%(T)(HPLC)Color and Shape:White to Orange to Green powder to crystalMolecular weight:149.166-(Methylamino)purine
CAS:Controlled Product<p>Applications 6-(Methylamino)purine, 6-methylade is a reagent for substitution of adenine nucleotide analogs containing bicyclohexane ring system locked in northern conformation enhanced potency as py receptor antagonists. Adenine methylation as an epigenic mark has been observed in single-celled organisms and also rarely in mamalian cells.<br>References Nandanan et al.: J. Med. Chem., 43, 829 (2000); Kim, H. S. et al.: J. Med. chem., 46, 4974 (2003); Chem. and Eng. News p.6 Apr. 4 (2016)<br></p>Formula:C6H7N5Color and Shape:NeatMolecular weight:149.15N-Methyl-7H-purin-6-amine
CAS:Formula:C6H7N5Purity:95%Color and Shape:Liquid, No data available.Molecular weight:149.1576-(Methylamino)purine-13C2,15N
CAS:Controlled ProductFormula:C2C4H715NN4Color and Shape:NeatMolecular weight:152.1326-(Methylamino)purine-d3
CAS:Controlled ProductFormula:C6D3H4N5Color and Shape:NeatMolecular weight:152.172N6-Methyladenine
CAS:<p>N6-Methyladenine is a modification of adenine in DNA. It is formed by the methylation of the N6 position of adenine, which is a group P2 purine base. The structural analysis of this compound has been studied using x-ray diffraction data, and it has been found that it may inhibit cancer cells by modifying their DNA. This compound can also be used as an antimicrobial agent to treat infections caused by eukaryotes such as bacteria and fungi. N6-Methyladenine may be useful in transcriptional regulation and cellular transformation.</p>Formula:C6H7N5Purity:Min. 95%Color and Shape:PowderMolecular weight:149.15 g/mol






