CAS 443-72-1
:N6-Methyladenine
- 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
1H-Purin-6-amine, N-methyl-
CAS:Formula:C6H7N5Purity:95%Color and Shape:SolidMolecular weight:149.1533N6-Methyladenine
CAS:N6-Methyladenine (6-(Methylamino)Purine) is a modified purine commonly found in genomes of prokaryotes, protists, and plants.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 ProductApplications 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.
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)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: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.
Formula:C6H7N5Purity:Min. 95%Color and Shape:PowderMolecular weight:149.15 g/mol






