Chemical Structure : HPK1-IN-3
货号: PC-22569Not For Human Use, Lab Use Only.
HPK1-IN-3 is a potent, selective, ATP-competitive hematopoietic progenitor kinase 1 (HPK1, MAP4K1) inhibitor with IC50 of 0.25 nM in TR-FRET assays.
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HPK1-IN-3 is a potent, selective, ATP-competitive hematopoietic progenitor kinase 1 (HPK1, MAP4K1) inhibitor with IC50 of 0.25 nM in TR-FRET assays.
HPK1-IN-3 exhibits HPK1 target engagement with EC50 of 453 nM in PBMCs.
HPK1-IN-3 displays >100x selectivity in 252/265 kinases examined.
分子量 | 490.46 | |
分子式 | C23H22F4N6O2 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
1. Brandon A Vara, et al. ACS Med Chem Lett. 2021 Mar 19;12(4):653-661.
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