Chemical Structure : LZK PROTAC 17
货号: PC-24506Not For Human Use, Lab Use Only.
LZK PROTAC 17 is a potent, selective PROTAC degrader of leucine zipper-bearing kinase (LZK, MAP3K13) with binding Kd of 71 nM, potently degrades LZK at 250 nM and suppresses HNSCC viability at 500 nM.
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LZK PROTAC 17 is a potent, selective PROTAC degrader of leucine zipper-bearing kinase (LZK, MAP3K13) with binding Kd of 71 nM, potently degrades LZK at 250 nM and suppresses HNSCC viability at 500 nM.
LZK PROTAC 17 (250 nM) reduces colony formation of CAL33 and DETROIT562.
LZK PROTAC 17 induces dose- and time-dependent degradation of LZK in HNSCC cells harboring MAP3K13 amplification.
分子量 | 909.11 | |
分子式 | C48H58F2N10O4S | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
1. Katerji M, et al. J Biol Chem. 2025 Mar 27:108452.
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