Chemical Structure : A-910
Catalog No.: PC-23041Not For Human Use, Lab Use Only.
A-910 is a highly potent and selective, orally active dual MerTK/Axl inhibitor with IC50 of 0.2/0.9 nM respectively, >200-fold selective over Tyro3.
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A-910 is a highly potent and selective, orally active dual MerTK/Axl inhibitor with IC50 of 0.2/0.9 nM respectively, >200-fold selective over Tyro3.
A-910 exhibits similar biochemical and Ba/F3 cellular potency (IC50=4.2 nM), shows EC50 of 4.0 and 8.0 nM in in vitro efferocytosis and pMerTK assays respectively.
A-910 exhibits favorable oral bioavailability, exceptional kinome selectivity, and significantly improved in vivo target engagement.
M.Wt | 694.85 | |
Formula | C40H47FN6O4 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Yu Y, et al. J Med Chem. 2024 Sep 16. doi: 10.1021/acs.jmedchem.4c01450.
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