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BAY 2476568

Chemical Structure : BAY 2476568

CAS No.: 2311901-93-4

BAY 2476568 (BAY-568)

Catalog No.: PC-23314Not For Human Use, Lab Use Only.

BAY 2476568 (BAY-598) is the first reversible, potent and selective inhibitor of EGFR exon 20 insertions with IC50 of 20 and 24 nM for V769_D770insASV (insASV) and D770_N771insSVD (insSVD), with a wide margin of selectivity versus WT EGFR.

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5 mg $288 In stock
10 mg $458 In stock
25 mg $758 In stock
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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

BAY 2476568 (BAY-598) is the first reversible, potent and selective inhibitor of EGFR exon 20 insertions with IC50 of 20 and 24 nM for V769_D770insASV (insASV) and D770_N771insSVD (insSVD), with a wide margin of selectivity versus WT EGFR.
BAY 2476568 (BAY-598) exhibits greater than 20-fold selectivity for EGFR exon 20 insertions compared to wild-type EGFR in isogenic Ba/F3 models and in cancer cell lines endogenously expressing EGFR exon 20 insertions.
BAY 2476568 (BAY-598) demonstrates the ability of BAY-568 to kill cancer cells harboring exon 20 insertions and other EGFR mutations with decreased activity on wild-type EGFR, irrespective of C797S mutation status.

Physicochemical Properties

M.Wt 454.50
Formula C24H27FN4O4
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
Solubility

10 mM in DMSO

Chemical Name/SMILES

3-[(3-Fluoro-2-methoxyphenyl)amino]-1,5,6,7-tetrahydro-2-[3-(2-methoxy-2-methylpropoxy)-4-pyridinyl]-4H-pyrrolo[3,2-c]pyridin-4-one

References

1. Patent WO2019081486A1.

2. F. Siegel et al. Cancer Res. 81, 1470–1470 (2021).

3. Hanchen Zhao, et al. Proc Natl Acad Sci U S A. 2024 Nov 5;121(45):e2417144121.

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