| Weight | 135.13 g/mol |
|---|---|
| Formula | C5H5N5 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
adenine (73-24-5)
Vitamin B 4
Score:
#776 in Biochemistry
,
#2117 in Biology
,
#2599 in Chemistry
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- The redox state of free nicotinamide-adenine dinucleotide in the cytoplasm and mitochondria of rat liver (Biochemical Journal, 1967)
- The physiological activity of adenine compounds with especial reference to their action upon the mammalian heart. (The Journal of Physiology, 1929)
- Bax and adenine nucleotide translocator cooperate in the mitochondrial control of apoptosis (Science, 1998)
- LNA (Locked Nucleic Acids): Synthesis of the adenine, cytosine, guanine, 5-methylcytosine, thymine and uracil bicyclonucleoside monomers, oligomerisation, and unprecedented nucleic acid recognition (Tetrahedron, 1998)
- DNA-mediated transfer of the adenine phosphoribosyltransferase locus into mammalian cells. (Proceedings of the National Academy of Sciences of the United States of America, 1979)
- DNA bending at adenine thymine tracts (Nature, 1986)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Vitamin B 4
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SMILESC1=NC2=C(N1)C(=NC=N2)N
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InChIKeyGFFGJBXGBJISGV-UHFFFAOYSA-N
- Pubchem - adenine
- Wikipedia - adenine
Adenine (A, Ade) is a nucleobase (a purine derivative). Its derivatives have a variety of roles in biochemistry including cellular respiration, in the form of both the energy-rich adenosine triphosphate (ATP) and the cofactors nicotinamide adenine dinucleotide (NAD) and flavin adenine dinucleotide (FAD). It also has functions in protein synthesis and as a chemical component of DNA and RNA.
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adenine
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