Basic information Safety Supplier Related

4,6-DIAMINO-5-(FORMYLAMINO)-PYRIMIDINE

Basic information Safety Supplier Related

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
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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
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Safety Information

WGK Germany 
3

MSDS

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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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