| Weight | 135.13 g/mol |
|---|---|
| Formula | C5H5N5 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
2-aminopurine (452-06-2)
2 Aminopurine
Score:
#1940 in Physics
,
#2430 in Biochemistry
,
#6080 in Chemistry
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- Fluorescence Studies of Nucleotides and Polynucleotides I. FORMYCIN, 2-AMINOPURINE RIBOSIDE, 2,6-DIAMINOPURINE RIBOSIDE, AND THEIR DERIVATIVES (Journal of Biological Chemistry, 1969)
- Probing structure and dynamics of DNA with 2-aminopurine: effects of local environment on fluorescence. (Biochemistry, 2001)
- 2-Aminopurine fluorescence quenching and lifetimes: Role of base stacking (Proceedings of the National Academy of Sciences of the United States of America, 2001)
- Adenine and 2-aminopurine: Paradigms of modern theoretical photochemistry (Proceedings of the National Academy of Sciences of the United States of America, 2006)
- 2-Aminopurine selectively inhibits the induction of beta-interferon, c-fos, and c-myc gene expression (Science, 1988)
- 2-Aminopurine fluorescence studies of base stacking interactions at abasic sites in DNA: metal-ion and base sequence effects (Nucleic Acids Research, 1998)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2 Aminopurine
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SMILESC1=C2C(=NC(=N1)N)N=CN2
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InChIKeyMWBWWFOAEOYUST-UHFFFAOYSA-N
- Pubchem - 2-aminopurine
- Wikipedia - 2-aminopurine
2-Aminopurine, an analog of guanine and adenine, is a fluorescent molecular marker used in nucleic acid research. It most commonly pairs with thymine as an adenine-analogue, but can also pair with cytosine as a guanine-analogue;. For this reason it is sometimes used in the laboratory for mutagenesis.
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2-aminopurine
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