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azd1390
Cat. No.:
OB0225WX-2348
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, and LC-MS.
Size:
Add to basket
Product Overview
Description:
AZD1390 is an exceptionally potent cellular ATM inhibitor (IC50: 0.78 nM) characterized by its 10,000-fold selectivity over other enzymes in the PIKK family.
Synonym:
AZD1390; 2089288-03-7; AZD-1390; 7-fluoro-3-methyl-8-[6-(3-piperidin-1-ylpropoxy)pyridin-3-yl]-1-propan-2-ylimidazo[4,5-c]quinolin-2-one; Azd 1390; 7-fluoro-1-isopropyl-3-methyl-8-(6-(3-(piperidin-1-yl)propoxy)pyridin-3-yl)-1,3-dihydro-2H-imidazo[4,5-c]quinolin-2-one; 2H-Imidazo(4,5-C)quinolin-2-one, 7-fluoro-1,3-dihydro-3-methyl-1-(1-methylethyl)-8-(6-(3-(1-piperidinyl)propoxy)-3-pyridinyl)-; 7-Fluoro-1-isopropyl-3-methyl-8-(-(3-(1-piperidinyl)propoxy)-3-pyridinyl)-1,3-dihydro-2himidazo(4,5-C)quinolin-2-one; 7-fluoro-1-isopropyl-3-methyl-8-(6-(3-(piperidin-1-yl)propoxy)pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-2(3H)-one; 7-fluoro-3-methyl-8-(6-(3-piperidin-1-ylpropoxy)pyridin-3-yl)-1-propan-2-ylimidazo(4,5-c)quinolin-2-one; 7-fluoro-1-isopropyl-3-methyl-8-{6-[3-(piperidin-1-yl)propoxy]pyridin-3-yl}imidazo[4,5-c]quinolin-2-one
CAS No.:
2089288-03-7
Compound CID:
126689157
Formula:
C27H32FN5O2
Formula Weight:
477.57
Specification
Targets&IC50:
ATM: 0.78 nM (cell based)
Relative Density:
1.224 g/cm3
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
azd1390 is employed in advanced neurological research as a highly potent, brain-permeable ATM inhibitor to study the sensitization of glioma cells to radiation-induced DNA damage.
Library Information
Target:
ATM/ATR
Receptor:
ATM
Pathways:
DNA damage/DNA repair; PI3K/Akt/mTOR signaling
Plate Number:
AOCL-31
Plate Location:
a10
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
2mM DMSO
DMSO Max Solubility:
4.77 mg/mL; 9.98 mM





