Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.
Visit our FAQ
Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888
Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

TM-2-51 is an activator of histone deacetylase 8 (HDAC8).1,2 It inhibits the growth of SH-SY5Y neuroblastoma cells expressing wild-type p53 when used at concentrations of 10, 40, and 80 µM.1 TM-2-51 (80 µM) induces apoptosis in the same cells but not in BE(2)-C neuroblastoma cells expressing mutant p53. TM-2-51 inhibits growth and migration of U2OS and 143B osteosarcoma cells in vitro and inhibits tumor growth in a 143B mouse xenograft model when administered at a dose of 10 mg/kg.3
WARNING This product is not for human or veterinary use.
1. Mechanism of N-
2. Histone deacetylase activators: N-
3. Activation of HDAC8 can suppress the proliferation of osteosarcoma cells via TP53 and STAT3/ERK signaling pathways. Ann. Clin. Lab. Sci. 53(6), 920-930 (2023).