| Weight | 149.157 g/mol |
|---|---|
| Formula | C6H7N5 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
N6-Methyladenine (443-72-1)
6-methyladenine · 6-methylaminopurine · N(6)-methyladenine
Score:
#1854 in Biochemistry
,
#4002 in Biology
,
#5043 in Chemistry
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- Escherichia coli, Saccharomyces cerevisiae, rat and human 3-methyladenine DNA glycosylases repair 1,N6-ethenoadenine when present in DNA. (Nucleic Acids Research, 1995)
- Biological function for 6-methyladenine residues in the DNA of Escherichia coli K12 (Journal of Molecular Biology, 1974)
- Induced mutagenesis in dam- mutants of Escherichia coli: a role for 6-methyladenine residues in mutation avoidance. (Molecular Genetics and Genomics, 1978)
- N6-Methyladenine DNA Modification in Drosophila (Cell, 2015)
- The occurrence of 6-methylaminopurine in deoxyribonucleic acids (Biochemical Journal, 1958)
- N6-methyladenine: the other methylated base of DNA. (BioEssays, 2006)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 6-methyladenine
- 6-methylaminopurine
- N(6)-methyladenine
-
SMILESCNC1=NC=NC2=C1NC=N2
-
InChIKeyCKOMXBHMKXXTNW-UHFFFAOYSA-N
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