Chemical Structure : ST-5-002
Catalog No.: PC-24008Not For Human Use, Lab Use Only.
ST-5-002 is a specific small molecule inhibitor of transmembrane 4 L six family member 5 (TM4SF5), inhibits signaling lymphocytic activation molecule family member 7 (SLAMF7) degradation due to TM4SF5 binding and lysosomal translocation.
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ST-5-002 is a specific small molecule inhibitor of transmembrane 4 L six family member 5 (TM4SF5), inhibits signaling lymphocytic activation molecule family member 7 (SLAMF7) degradation due to TM4SF5 binding and lysosomal translocation.
ST-5-002 reduces colocalization of TM4SF5 and SLAMF7 at lysosomes, leaving more SLAMF7 at the plasma membrane, recovers TM4SF5-dependent decrease in SLAMF7.
TM4SF5 bound SLAMF7 depending on N-glycosylation and caused intracellular trafficking of SLAMF7 from the plasma membrane to lysosomes for degradation.
ST-5-002 inhibits SLAMF7 degradation due to TM4SF5 binding and lysosomal translocation.
ST-5-002 (5 mpk, i.p.) recovered SLAMF7-positive cell populations to block cellular growth.
ST-5-002 abrogates HCC development by increasing the abundance and dispersion of Slamf7-positive cells in liver tissues, recapitulating the phenotype of Tm4sf5-knockout mice and indicating TSI-mediated restoration of NK cell surveillance.
M.Wt | 370.41 | |
Formula | C23H18N2O3 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Kim JE, et al. Signal Transduct Target Ther. 2025 Jan 20;10(1):15.
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