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CA-4948

Chemical Structure : CA-4948

CAS No.: 1801344-14-8

CA-4948 (Emavusertib;CA4948;AU-4948;AU4948)

Catalog No.: PC-50002Not For Human Use, Lab Use Only.

Emavusertib (CA-4948) is a potent, selective and orally active IRAK4 inhibitor with IC50 of 31.7 nM.

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Biological Activity

Emavusertib (CA-4948) is a potent, selective and orally active IRAK4 inhibitor with IC50 of 31.7 nM.
Emavusertib (CA-4948) exhibits significant activity against a handful of other kinases such as CLK1, CLK2, CLK4, FLT3, DYRK1A, DYRK1B, TrkA, TrkB, Haspin, and NEK11 in a panel of a broad kinome panel (329 kinases).
Emavusertib (CA-4948) showed good modulation of IL6 in human whole blood assayand pIRAK1 modulation (IC50 of 270 nM) in MV4-11 cell-line.
Emavusertib (CA-4948) demonstrated moderate potency in OCI-Ly10 (IC50 = 1.5 μM) harboring MYD88 mutation in cellular growth inhibition assay in a short panel of lymphoma cell lines.
Emavusertib (CA-4948) showed >90% tumor growth inhibition in relevant tumor models with excellent correlation with in vivo PD modulation.

Physicochemical Properties

M.Wt 491.508
Formula C24H25N7O5
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping Room temperature in continental US; may vary elsewhere
Solubility

10 mM in DMSO

Chemical Name/SMILES

N-[5-[(3R)-3-Hydroxy-1-pyrrolidinyl]-2-(4-morpholinyl)oxazolo[4,5-b]pyridin-6-yl]-2-(2-methyl-4-pyridinyl)-4-oxazolecarboxamide

References

1. Robert Booher, et al. 1534 Combination of IRAK4 Inhibitor CA-4948 with BCL2 Inhibitor Venetoclax Induces Tumor Regression in an ABC-DLBCL Xenograft Model. Bldg A, Lvl 1, Hall A2 (Georgia World Congress Center).
2. Gummadi VR, et al. ACS Med Chem Lett. 2020 Oct 14;11(12):2374-2381.
3. Zhang S, et al. Front Immunol. 2021 Mar 9;12:637659.

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