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1821428-35-6

1821428-35-6 structure
1821428-35-6 structure
  • Name: AZD-0156
  • Chemical Name: 8-{6-[3-(Dimethylamino)propoxy]-3-pyridinyl}-3-methyl-1-(tetrahydro-2H-pyran-4-yl)-1,3-dihydro-2H-imidazo[4,5-c]quinolin-2-one
  • CAS Number: 1821428-35-6
  • Molecular Formula: C26H31N5O3
  • Molecular Weight: 461.556
  • Catalog: Signaling Pathways Cell Cycle/DNA Damage ATM/ATR
  • Create Date: 2018-01-05 04:45:18
  • Modify Date: 2024-01-02 19:15:59
  • AZD0156 is an oral, potent and selective ATM inhibitor with an IC50 of 0.58 nM.

Name 8-{6-[3-(Dimethylamino)propoxy]-3-pyridinyl}-3-methyl-1-(tetrahydro-2H-pyran-4-yl)-1,3-dihydro-2H-imidazo[4,5-c]quinolin-2-one
Synonyms 8-{6-[3-(Dimethylamino)propoxy]-3-pyridinyl}-3-methyl-1-(tetrahydro-2H-pyran-4-yl)-1,3-dihydro-2H-imidazo[4,5-c]chinolin-2-on
2H-Imidazo[4,5-c]quinolin-2-one, 8-[6-[3-(dimethylamino)propoxy]-3-pyridinyl]-1,3-dihydro-3-methyl-1-(tetrahydro-2H-pyran-4-yl)-
8-{6-[3-(Dimethylamino)propoxy]-3-pyridinyl}-3-methyl-1-(tetrahydro-2H-pyran-4-yl)-1,3-dihydro-2H-imidazo[4,5-c]quinolin-2-one
8-{6-[3-(Diméthylamino)propoxy]-3-pyridinyl}-3-méthyl-1-(tétrahydro-2H-pyran-4-yl)-1,3-dihydro-2H-imidazo[4,5-c]quinoléin-2-one
AZD-0156
AZD0156
Description AZD0156 is an oral, potent and selective ATM inhibitor with an IC50 of 0.58 nM.
Related Catalog
Target

ATM

In Vitro AZD0156 inhibits the kinase activity of ATM and ATM-mediated signaling, prevents DNA damage checkpoint activation, and disrupts DNA damage repair, inducs tumor cell apoptosis, and leads to cell death in ATM-overexpressing tumor cells[1].
Cell Assay HT29 cells are seeded into 384 well assay plates at a density of 6000 cells/well in 40 μL EMEM medium containing 1% L glutamine and 10% FBS and allowed to adhere overnight. The following morning compound of Formula (I) in 100% DMSO is added to assay plates by acoustic dispensing. After lh incubation at 37°C and 5% C02, 40 nL of 3 mM 4NQO in 100% DMSO is added to all wells by acoustic dispensing, except minimum control wells which are left untreated with 4NQO to generate a null response control. Plates are returned to the incubator for a further lh. Then cells are fixed by adding 20 μL of 3.7% formaldehyde in PBS solution and incubating for 20 mins at r.t.. Then 20 μL of 0.1% Triton XI 00 in PBS is added and incubated for 10 minutes at r.t., to permeabalise cells. Then the plates are washed once with 50 μL/well PBS, using a Biotek EL405 plate washer.
References

[1]. Imidazo[4,5-c]quinolin-2-one compounds and their use in treating cancer.?

Density 1.2±0.1 g/cm3
Boiling Point 628.3±55.0 °C at 760 mmHg
Molecular Formula C26H31N5O3
Molecular Weight 461.556
Flash Point 333.8±31.5 °C
Exact Mass 461.242676
LogP 2.40
Appearance white solid
Vapour Pressure 0.0±1.8 mmHg at 25°C
Index of Refraction 1.626
Storage condition -20℃