6-Hydroxy-2,4,5-triaminopyrimidine
CAS No.:
1004-75-7
M. Wt:
141.131
M. Fa:
C4H7N5O
InChI Key:
SYEYEGBZVSWYPK-UHFFFAOYSA-N
Appearance:
Solid
Names and Identifiers of 6-Hydroxy-2,4,5-triaminopyrimidine
CAS Number |
1004-75-7 |
|---|---|
EC Number |
213-725-4 |
MDL Number |
MFCD00217058 |
IUPAC Name |
2,4,5-triamino-1H-pyrimidin-6-one |
InChI |
InChI=1S/C4H7N5O/c5-1-2(6)8-4(7)9-3(1)10/h5H2,(H5,6,7,8,9,10) |
InChIKey |
SYEYEGBZVSWYPK-UHFFFAOYSA-N |
Canonical SMILES |
C1(=C(N=C(NC1=O)N)N)N |
UNII |
FR001FJW89 |
UNSPSC Code |
12352100 |
Physical and chemical properties of 6-Hydroxy-2,4,5-triaminopyrimidine
Boiling Point |
534.6±60.0 °C at 760 mmHg |
|---|---|
Density |
1.7±0.1 g/cm3 |
Exact Mass |
141.065063 |
Flash Point |
277.1±32.9 °C |
Index of Refraction |
1.875 |
LogP |
-0.88 |
Molecular Formula |
C4H7N5O |
Molecular Weight |
141.131 |
PSA |
124.07000 |
Vapour Pressure |
0.0±1.5 mmHg at 25°C |
Safety Information of 6-Hydroxy-2,4,5-triaminopyrimidine
Applications of 6-Hydroxy-2,4,5-triaminopyrimidine
6-Hydroxy-2,4,5-triaminopyrimidine has various applications:
- Intermediate in Synthesis: It serves as an intermediate for synthesizing labeled substituted 5-aminopyrimidines with antioxidative activity.
- Biochemical Research: Its role in modulating gene expression makes it valuable in biochemical studies related to cellular processes.
- Potential Therapeutics: Due to its biological activity and interactions with biomolecules, it may have potential therapeutic applications.
Interaction Studies of 6-Hydroxy-2,4,5-triaminopyrimidine
Studies on the interactions of 6-Hydroxy-2,4,5-triaminopyrimidine indicate its capability to modulate cellular functions through binding to riboswitches. This interaction can lead to significant changes in gene expression patterns and metabolic pathways within cells. Its antioxidant properties also suggest potential protective roles against oxidative stress in biological systems.
Biological Activity of 6-Hydroxy-2,4,5-triaminopyrimidine
This compound exhibits significant biological activity:
- Role as a Chromophore: It functions as a chromophore, absorbing light and potentially influencing various biological processes.
- Antioxidant Properties: 6-Hydroxy-2,4,5-triaminopyrimidine has been identified as an antioxidant, indicating its ability to neutralize free radicals.
- Interaction with Riboswitches: It binds to riboswitches, regulatory elements that modulate gene expression in response to specific metabolites. This interaction can influence cellular metabolism and gene expression pathways.
Physical sample testing spectrum (NMR) of 6-Hydroxy-2,4,5-triaminopyrimidine
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