4,6-DIAMINO-5-(FORMYLAMINO)-PYRIMIDINE
4,6-DIAMINO-5-(FORMYLAMINO)-PYRIMIDINE Basic information
- Product Name:
- 4,6-DIAMINO-5-(FORMYLAMINO)-PYRIMIDINE
- Synonyms:
-
- 4,6-diamino-5-n-formamidopyrimidine
- 4,6-Diaminobenzene-5-formamidopyrimide-formyl-13C, diamino-15N2
- 4,6-DIAMONO-5-(FORMYLAMINO)PYRIMIDNE
- FAPy-adenine
- DIAMINO-15N2)
- FAPYADENINE(FORMYL-13C
- DIAMINO-15N2, 98%)
- 4,6-Diamino-5-(Formylamino)-Pyrimidine HCl
- CAS:
- 5122-36-1
- MF:
- C5H7N5O
- MW:
- 153.14
- EINECS:
- 200-258-5
- Product Categories:
-
- Biochemicals and Reagents
- Nucleoside Analogs
- Nucleosides, Nucleotides, Oligonucleotides
- Mol File:
- 5122-36-1.mol
4,6-DIAMINO-5-(FORMYLAMINO)-PYRIMIDINE Chemical Properties
- Melting point:
- 224-226 °C
- Boiling point:
- 536.1±50.0 °C(Predicted)
- Density
- 1.575±0.06 g/cm3(Predicted)
- storage temp.
- −20°C
- pka
- 12.35±0.70(Predicted)
- form
- Solid
- color
- Off-white to light yellow
MSDS
- Language:English Provider:SigmaAldrich
4,6-DIAMINO-5-(FORMYLAMINO)-PYRIMIDINE Usage And Synthesis
Uses
FAPy-adenine is an oxidized DNA base. Fapy-adenine shows an increased trend levels in the Alzheimer's disease brain. Oxidized nucleosides are biochemical markers for tumors, aging, and neurodegenerative diseases[1][2][3].
Definition
ChEBI: A member of the class of aminopyrimidines that is 4,6-diaminopyrimidine bearing an additional formamido substituent at position 5. A DNA lesion formed when DNA exposed to ionising radiation.
in vivo
The nuclear DNA damage by oxygen-derived radicals is increased in Alzheimer's disease and support the concept that the brain is under increased oxidative stress in Alzheimer's disease[1].
IC 50
Human Endogenous Metabolite
References
[1] Gabbita SP, et al. Increased nuclear DNA oxidation in the brain in Alzheimer's disease. DOI:10.1046/j.1471-4159.1998.71052034.x
[2] Cysewski P, et al. Theoretical description of the coding potential of diamino-5-formamidopyrimidines. Z Naturforsch C J Biosci. 1999 Mar-Apr;54(3-4):239-45. DOI:10.1515/znc-1999-3-414
[3] Lee SH, et al. A rapid and sensitive method for quantitation of nucleosides in human urine using liquid chromatography/mass spectrometry with direct urine injection. Rapid Commun Mass Spectrom. 2004;18(9):973-7. DOI:10.1046/j.1471-4159.1998.71052034.x
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