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ST-5-002

Chemical Structure : ST-5-002

CAS No.:

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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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

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.

Physicochemical Properties

M.Wt 370.41
Formula C23H18N2O3
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
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Solubility

10 mM in DMSO

Chemical Name/SMILES

N-(4-(3-(4-Hydroxyphenyl)isoxazol-5-yl)phenyl)-4-methylbenzamide

References

1. Kim JE, et al. Signal Transduct Target Ther. 2025 Jan 20;10(1):15.

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