An activator of HDAC8
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TM-2-51

Item No. 45129

Technical Information
Formal Name
N-[(phenylamino)thioxomethyl]-benzamide
CAS Number
4921-82-8
Synonyms
  • NSC 5817
Molecular Formula
C14H12N2OS
Formula Weight
Purity
≥95%
A crystalline solid
DMSO: Sparingly soluble: 1-10 mg/ml
SMILES
S=C(NC(C1=CC=CC=C1)=O)NC2=CC=CC=C2
InChi Code
InChI=1S/C14H12N2OS/c17-13(11-7-3-1-4-8-11)16-14(18)15-12-9-5-2-6-10-12/h1-10H,(H2,15,16,17,18)
InChi Key
GVHZQIIMGRLFMX-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    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.

    References & Product Citations
    Product Description References

    1. Singh, R.K., Cho, K., Padi, S.K., et alMechanism of N-Acylthiourea-mediated activation of human histone deacetylase 8 (HDAC8) at molecular and cellular levels. The Journal of Biological Chemisty 290(10), 6607-6619 (2015).

    2. Singh, R.K., Mandal, T., Balsubramanian, N., et alHistone deacetylase activators: N-acetylthioureas serve as highly potent and isozyme selective activators for human histone deacetylase-8 on a fluorescent substrate. Bioorg. Med. Chem. Lett. 21(19), 5920-5923 (2011).

    3. Wang, L., Bai, X., Zhang, X., et alActivation 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).