Chemical Structure : Mesinostat
Catalog No.: PC-25904Not For Human Use, Lab Use Only.
Mesinostat is a potent and selective HDAC6 inhibitor with IC50 of 7.7 nM, >200-fold selective over HDAC1.
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Mesinostat is a potent and selective HDAC6 inhibitor with IC50 of 7.7 nM, >200-fold selective over HDAC1.
Mesinostat inhibits the growth of MDA-MB-231 cells with IC50 of 11 uM (48 h), induces α-tubulin acetylation. Mesinostat induces apoptosis in MDA-MB-231 cells.
Mesinostat significantly increases the expression of LC3II protein, promotes autophagy in human TNBC cells, induces cell cycle arrest.
Mesinostat suppresses epithelial-mesenchymal transition (EMT) in human TNBC cells, inhibits cell migration and colony formation.
Mesinostat (1-10 uM) reduces viability and stem-like properties in lymph node metastasis-derived TNBC organoids
| M.Wt | 412.47 | |
| Formula | C22H25FN4O3 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Bello I, et al. Pharmacol Res. 2025 Dec 2;222:108055.
2. Barone S, et al. Eur J Med Chem. 2025 Aug 5;292:117634.

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