N 6 -methyladenine
Structural formula | |||||||||||||||||||
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General | |||||||||||||||||||
Surname | N 6 -methyladenine | ||||||||||||||||||
other names |
6-methylamino-purine |
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Molecular formula | C 6 H 7 N 5 | ||||||||||||||||||
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properties | |||||||||||||||||||
Molar mass | 149.15 g mol −1 | ||||||||||||||||||
Physical state |
firmly |
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safety instructions | |||||||||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
N 6 -Methyladenine is a heterocyclic organic compound with a purine backbone. It is a derivative of the nucleobase adenine , whichis methylated at the amino group . It occurs as a component of the nucleoside N 6 -methyladenosine (m 6 A) in RNA and also in bacterial DNA .
The dimethylated variant is N 6 , N 6 -dimethyladenine .
Individual evidence
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ↑ D. Ratel, JL Ravanat, F. Berger, D. Wion: "N6-methyladenine: the other methylated base of DNA", Bioessays , 2006 , 28 (3), pp. 309-315 ( PMC 2754416 (free full text) ; PMID 16479578 ).
- ↑ Melanie Ehrlich, Miguel A. Gama-Sosa, Laura H. Carreira, Lars G. Ljungdahl, Kenneth C. Kuo, Charles W. Gehrke: "DNA methylation in thermophilic bacteria: N 4 -methylcytosine, 5-methylcytosine, and N 6 -methyladenine ", Nucleic Acids Research , 1985 , 13 (4), pp. 1399-1412 ( doi : 10.1093 / nar / 13.4.1399 ; PMC 341080 (free full text); PMID 4000939 ).