Chemical Structure : AZ13711265
货号: PC-63151Not For Human Use, Lab Use Only.
AZ13711265 is a potent, selective, in vivo active PAK1 inhibitor with IC50 of 0.58 nM, displays 880-, 2100- and 90-fold selectivity over Src, FGFR1, KDR and PAK4.
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AZ13711265 is a potent, selective, in vivo active PAK1 inhibitor with IC50 of 0.58 nM, displays 880-, 2100- and 90-fold selectivity over Src, FGFR1, KDR and PAK4.
AZ13711265 inhibits cellular pPAK1 inhibition in MCF10A cell line with IC50 of 110 nM.
AZ13711265 is an in vivo probe compound with oral exposure in mouse.
分子量 | 554.685 | |
分子式 | C28H35FN6O3S | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
1. McCoull W, et al. ACS Med Chem Lett. 2016 Sep 14;7(12):1118-1123.
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