ChemicalBook--->CAS DataBase List--->1370544-73-2

1370544-73-2

1370544-73-2 Structure

1370544-73-2 Structure
IdentificationBack Directory
[Name]

AX-024 hcl
[CAS]

1370544-73-2
[Synonyms]

CS-2619
AX-024 hcl
AX 024;AX024
Pyrrolidine, 1-[[4-(4-fluorophenyl)-6-methoxy-2H-1-benzopyran-3-yl]methyl]-
[Molecular Formula]

C21H22FNO2
[MOL File]

1370544-73-2.mol
[Molecular Weight]

339.4
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMSO:35.0(Max Conc. mg/mL);103.12(Max Conc. mM)
Ethanol:100.0(Max Conc. mg/mL);294.63(Max Conc. mM)
Hazard InformationBack Directory
[Description]

AX-024 is an inhibitor of the TCR-Nck interaction that selectively inhibits TCR-triggered T cell activation. AX-024 modulates cell signaling by targeting SH3 domains and has low-acute toxicity and high potency and selectivity in the inhibition of the production of IL-6, TNF-α, IFN-γ, IL-10 and IL-17A.
[Uses]

AX-024, is >10,000-fold more potent than the AX-000 hit in terms of inhibition of TCR-triggered T cell proliferation. It is a cytokine release inhibitor which can strongly inhibit the production of interleukin-6 (IL-6), tumor necrosis factor-α (TNFα), interferon-γ (IFN-γ), IL-10 and IL-17A.
[in vitro]

AX-024 reduces T cell proliferation upon weak T cell receptor (TCR) stimulation but neither significantly affects phosphorylation of Zap70 (ζ chain of T cell receptor–associated protein kinase 70) nor interacts directly with Nck1-SH3. AX-024 is likely not involved in modulating the Nck/TCR interaction but probably has other targets in T cells. An array of biophysical techniques did not detect a direct interaction between AX-024 and Nck-SH3.1 in vitro._x000D_ _x000D_ Reference: J Biol Chem. 2020 Jun 5;295(23):7849-7864. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278359/#B11
[target]

AX-024 is an inhibitor of the TCR-Nck interaction that selectively inhibits TCR-triggered T cell activation with an IC50 ~1 nM.
[storage]

Store at -20°C
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