Abstract
6-Formylpterin (6FP) has been reported to produce reactive oxygen species (ROS) such as {radical dot} O2- and H2O2 from O2 in the presence of NADH under light condition. In the present study, we prepared a variety of 6FP derivatives and found that 2-(N,N-dimethylaminomethyleneamino)-6-formyl-3-pivaloylpteridin-4-one and 2-(N,N-dimethylaminomethyleneamino)-6-formyl-3-methylpteridin-4-one, in which the 2-amino groups are modified by a dimethylaminomethylene group and the 3-positions by pivaloyl and methyl groups and 2-amino-6-formyl-3-methylpteridin-4-one in which the amino group at the 2-position is free and the 3-position is modified by a methyl group generated H2O2 from O2 on oxidation of NADH to NAD+ in the dark. However, 6FP and 2-(N,N-dimethylaminomethyleneamino)-6-formylpteridin-4-one, in which the 3-position is free did not yield H2O2. These results indicate that modification of the 3-position is essential to make the activities of 6FP available in the dark and would be suggestive for designing pharmaceutical compounds that generate appropriate and controllable amounts of ROS in vivo.
| Original language | English |
|---|---|
| Pages (from-to) | 1105-1110 |
| Number of pages | 6 |
| Journal | Biochemical and biophysical research communications |
| Volume | 353 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 2007 Feb 23 |
| Externally published | Yes |
Keywords
- 6-Formylpterin
- 6-Formylpterin derivatives
- Generation of reactive oxygen species in the dark
- HO formation from O
- Oxidation of NADH to NAD
ASJC Scopus subject areas
- Biophysics
- Biochemistry
- Molecular Biology
- Cell Biology