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HDAC6 inhibitor DR-3

Chemical Structure : HDAC6 inhibitor DR-3

CAS No.: 2202244-44-6

HDAC6 inhibitor DR-3

Catalog No.: PC-24228Not For Human Use, Lab Use Only.

HDAC6 inhibitor DR-3 is a selective small molecule HDAC6 inhibitor with IC50 of 78.1 nM, shows 100-fold selectivity over HDAC1.

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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

HDAC6 inhibitor DR-3 is a selective small molecule HDAC6 inhibitor with IC50 of 78.1 nM, shows 100-fold selectivity over HDAC1.
DR-3 is effective for relieving HDAC6-mediated deacetylation of α-tubulin and exerts anti-fibrogenic effects at the transcript level in the human LX-2 hepatic myofibroblast line.
DR-3 (100 nM) suppresses hepatic stellate cell (HSC) expression of TGF-β1 mRNA in primary rat HSC, suppresses TGFβ1 induced profibrogenic SMAD signaling.
DR-3 shows antifibrogenic activities in human precision-cut liver slice cultures, prevents fibrosis progression in the diseased human liver.

Physicochemical Properties

M.Wt 236.27
Formula C12H16N2O3
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

N-hydroxy-4-(morpholinomethyl)benzamide

References

1. Borrello MT, et al. FEBS J. 2025 Mar 14. doi: 10.1111/febs.70062.

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