Products
Online Inquiry
Elimusertib
Cat. No.:
OB0225WX-2338
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, HPLC, and LC-MS.
Size:
Add to basket
Product Overview
Description:
Elimusertib is a highly selective and orally bioavailable ATR inhibitor with a nanomolar IC50 of 7 nM.
Synonym:
BAY-1895344; 1876467-74-1; BAY 1895344; BAY1895344; (R)-3-methyl-4-(4-(1-methyl-1H-pyrazol-5-yl)-8-(1H-pyrazol-3-yl)-1,7-naphthyridin-2-yl)morpholine; BAY-1895344 HCl; (3R)-3-methyl-4-[4-(2-methylpyrazol-3-yl)-8-(1H-pyrazol-5-yl)-1,7-naphthyridin-2-yl]morpholine; (3R)-3-methyl-4-(4-(2-methylpyrazol-3-yl)-8-(1H-pyrazol-5-yl)-1,7-naphthyridin-2-yl)morpholine; (R)-3-methyl-4-(4-(1-methyl-1H-pyrazol-5-yl)-8-(1H-pyrazol-5-yl)-1,7-naphthyridin-2-yl)morpholine; 2-[(3R)-3-Methyl-4-morpholinyl]-4-(1-methyl-1H-pyrazol-5-yl)-8-(1H-pyrazol-3-yl)-1,7-naphthyridine; BAY-1895344; 2-[(3R)-3-methylmorpholin-4-yl]-4-(2-methylpyrazol-3-yl)-8-(1H-pyrazol-3-yl)-1,7-naphthyridine
CAS No.:
1876467-74-1
Compound CID:
118869362
Formula:
C20H21N7
Formula Weight:
375.43
Specification
Targets&IC50:
ATR: 7 nM (IC50)
Relative Density:
1.43 g/cm3
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Elimusertib is utilized in advanced oncology research as a potent and selective ATR inhibitor to investigate the disruption of replication stress responses and the enhancement of DNA-damaging therapies.
Library Information
Target:
ATM/ATR
Receptor:
ATR
Pathways:
DNA damage/DNA repair; PI3K/Akt/mTOR signaling
Plate Number:
AOCL-30
Plate Location:
h10
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
11 mg/mL; 29.3 mM





