Chemical Structure : BAY 2476568
CAS No.: 2311901-93-4
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.
Packing | Price | Stock | Quantity |
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5 mg | $288 | In stock | |
10 mg | $458 | In stock | |
25 mg | $758 | In stock | |
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100 mg | Get quote |
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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.
M.Wt | 454.50 | |
Formula | C24H27FN4O4 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
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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 |
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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