Molecular Formula | C15H12N2O2 |
Molar Mass | 252.27 |
Density | 1.27±0.1 g/cm3(Predicted) |
Boling Point | 492.5±45.0 °C(Predicted) |
Solubility | DMSO : 125 mg/mL (495.50 mM; Need ultrasonic) |
Appearance | powder |
Color | yellow |
pKa | 9.30±0.20(Predicted) |
Storage Condition | 2-8°C |
In vitro study | In kinetic experiments with human PARP-1, BYK204165 exhibits potent and competitive inhibition of enzyme activity, yielding a pK i value of 7.05. BYK204165 exhibits low potency of PARP inhibition in C4I cells (pIC 50 of 5.75). |
In vivo study | BYK204165 is not investigated in vivo because of its short half-time (t 1/2 ) of 23 min measured at rat microsomes in vitro. |
Hazard Symbols | Xi - Irritant |
Risk Codes | 43 - May cause sensitization by skin contact |
Safety Description | 36/37 - Wear suitable protective clothing and gloves. |
WGK Germany | 3 |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 3.964 ml | 19.82 ml | 39.64 ml |
5 mM | 0.793 ml | 3.964 ml | 7.928 ml |
10 mM | 0.396 ml | 1.982 ml | 3.964 ml |
5 mM | 0.079 ml | 0.396 ml | 0.793 ml |
biological activity | BYK204165 is an effective selective inhibitor of poly(ADP-ribose) polymerase (PARP). The pIC50 and pKi values corresponding to human PARP-1 (hPARP-1) that BYK204165 can inhibit cell-free recombination are 7.35 and 7.05, respectively, and the pIC50 value for mouse PARP-2 (mPARP-2) is 5.38. |
target | cell-free hPARP-1 7.35(pIC50) hPARP-1 7.05(pKi) mPARP-2 5.38(pIC50) |
Target | Value |
hPARP-1 (Cell-free assay) | 7.35(pIC50) 7.05(pKi) |
mPARP-2 (Cell-free assay) | 5.38(pIC50) |
in vitro study | in kinetic experiments with human PARP-1, BYK204165 exhibits potent and competitive inhibition of enzyme activity, yielding a pK I value of 7.05. BYK204165 exhibits low potency of PARP inhibition in C4I cells (pIC 50 of 5.75). |
in vivo study | BYK204165 is not investigated in vivo because of its short half-time (t 1/2 ) of 23 min measured at rat microsomes in vitro. |