SALL4 inhibitor SH6

Chemical Structure : SALL4 inhibitor SH6

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货号: PC-24596Not For Human Use, Lab Use Only.

规格	价格	库存	数量
50 mg		Get quote
100 mg		Get quote
250 mg		Get quote

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生物&药学活性

SALL4 inhibitor SH6 is a small molecule inhibitor of transcription factor SALL4 ZFC4 domain, selectively targets SALL4-expressing cancer cells (EC50=0.5 uM, SNU398 cells), degrades SALL4 protein through the CUL4A/CRBN pathway.
SH6 targets SALL4 via a novel ZFC4 pocket domain.
SH6 displayed greater potencies against SALL4 expressing cancer cell lines H661, H838, and CAL51 (EC50 = 0.21 μM, 1.30 μM, and 0.54 μM, respectively) as compared to SALL4 low cell lines H552 and H2030 (EC50 = 48.4 μM, and 41.6 μM, respectively).
SH6 selectively kills SALL4 expressing liver cancer cells with EC50 values of 0.3 μM to 1.3 μM, but not non-transformed liver cell lines THLE-2 and THLE-3.
SH6 degrades SALL4B through the CUL4A-CRBN pathway, but failed to degrade SALL4B in the absence of ZFC4.
SH6 (20-40 mg/kg) significantly reduced tumor growth in mice with tumors derived from human cancer patients.

物理化学性质&存储条件

分子量	454.91
分子式	C23H23ClN4O4
外观性状	Solid
CAS No.
储存条件	固体粉末 -20°C 12 个月; 4°C 6 个月	配置液 -80°C 6 个月; -20°C 6 个月
Shipping
Solubility	10 mM in DMSO
Chemical Name/SMILES	(E)-N-(2-amino-5-chlorophenyl)-3-(2-((3,4,5-trimethoxyphenyl)amino)pyridin-3-yl)acrylamide

参考文献

1. Liu BH, et al. EMBO Mol Med. 2025 May 14. doi: 10.1038/s44321-025-00241-3.