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MPT0G521

Chemical Structure : MPT0G521

CAS No.: 3023019-99-7

MPT0G521 (HDAC6-IN-3)

Catalog No.: PC-28051Not For Human Use, Lab Use Only.

MPT0G521 (HDAC6-IN-3) is a potent, orally active dual KDM1A/class I HDAC inhibitor with IC50 of 0.02-1.54 uM for HDAC1/2/3/6/8/10, also inhibits lysine-specific demethylase 1A (KDM1A, LSD1).

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

MPT0G521 (HDAC6-IN-3) is a potent, orally active dual KDM1A/class I HDAC inhibitor with IC50 of 0.02-1.54 uM for HDAC1/2/3/6/8/10, also inhibits lysine-specific demethylase 1A (KDM1A, LSD1).
MPT0G521 elicits magnificent cell growth inhibitory effects against the PC-3 and DU-145 cell lines with GI50 of 0.33 uM and 0.42 uM respectively.
MPT0G521 inhibits KDM1A activity and alters histone modifications in GBM cells.
MPT0G521 triggers G2/M arrest followed by apoptotic sub-G1 accumulation.
MPT0G521 induces apoptotic signaling and suppresses Cyclin B1 in GBM cells.

Physicochemical Properties

M.Wt 345.44
Formula C19H27N3O3
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
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

N1-hydroxy-N8-(3-((methyl(prop-2-yn-1-yl)amino)methyl)phenyl)octanediamide

References

1. Ritu Ojha, et al. J Med Chem. 2021 Dec 23;64(24):17824-17845.

2. Wu AC, et al, Biochem Pharmacol. 2026 Sep 2:118415.

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