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CHIR-124
Cat. No.:
0225LY-1104
Appearance:
Solid
Purity:
≥98%
Identity:
Confirmed by NMR.
Size:
Add to basket
Product Overview
Description:
CHIR-124 serves as an efficient Chk1 inhibitor with an IC50 of 0.3 nM, providing 2,000-fold selectivity over Chk2 and significantly lower potency against CDK2/4 and Cdc2.
Synonym:
CHIR124; CHIR 124; 405168-58-3; (S)-3-(1H-benzo[d]imidazol-2-yl)-6-chloro-4-(quinuclidin-3-ylamino)quinolin-2(1H)-one; 4-[(3s)-1-Azabicyclo[2.2.2]oct-3-Ylamino]-3-(1h-Benzimidazol-2-Yl)-6-Chloroquinolin-2(1h)-One; 2(1H)-Quinolinone, 4-((3S)-1-azabicyclo(2.2.2)oct-3-ylamino)-3-(1H-benzimidazol-2-yl)-6-chloro-; 4-(((3S)-1-Azabicyclo(2.2.2)oct-3-yl)amino)-3-(1H-benzimidazol-2-yl)-6-chloroquinolin-2(1H)-one; 4-[[(3S)-1-azabicyclo[2.2.2]octan-3-yl]amino]-6-chloro-3-(1,3-dihydrobenzimidazol-2-ylidene)quinolin-2-one
CAS No.:
405168-58-3
Compound CID:
135399748
Formula:
C23H22ClN5
Formula Weight:
419.91
Specification
Targets&IC50:
Chk1: 0.3 nM
Relative Density:
1.46 g/cm3
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
CHIR-124 can be used in cell cycle research to study the selective inhibition of Chk1 and its potential in sensitizing tumor cells to DNA-damaging agents.
Library Information
Target:
FLT; GSK-3; Src; PDGFR; Chk
Receptor:
Chk1; FLT3; Fyn; GSK-3; PDGFR
Pathways:
Stem cell regulation; Apoptosis; PI3K/Akt/mTOR signaling; Angiogenesis; Cell cycle/Checkpoint; Tyrosine kinase/adaptors
Plate Number:
AOCL-15
Plate Location:
b10
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
15 mg/mL; 35.72 mM
Water Max Solubility:
<1 mg/mL (insoluble or slightly soluble)
Ethanol Max Solubility:
<1 mg/mL (insoluble or slightly soluble)





