ChemicalBook--->CAS DataBase List--->5122-36-1

5122-36-1

5122-36-1 Structure

5122-36-1 Structure
IdentificationBack Directory
[Name]

4,6-DIAMINO-5-(FORMYLAMINO)-PYRIMIDINE
[CAS]

5122-36-1
[Synonyms]

FAPy-adenine
DIAMINO-15N2)
DIAMINO-15N2, 98%)
FAPYADENINE(FORMYL-13C
4,6-diamino-5-n-formamidopyrimidine
4,6-DIAMONO-5-(FORMYLAMINO)PYRIMIDNE
N-(4,6-Diaminopyrimidin-5-yl)formamide
4,6-DIAMINO-5-(FORMYLAMINO)-PYRIMIDINE
Formamide, N-(4,6-diamino-5-pyrimidinyl)-
4,6-Diamino-5-(Formylamino)-Pyrimidine HCl
4,6-Diaminobenzene-5-formamidopyrimide-formyl-13C, diamino-15N2
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C5H7N5O
[MDL Number]

MFCD00047382
[MOL File]

5122-36-1.mol
[Molecular Weight]

153.14
Chemical PropertiesBack Directory
[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
[form ]

Solid
[pka]

12.35±0.70(Predicted)
[color ]

Off-white to light yellow
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[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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