Chemical Structure : 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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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.
M.Wt | 236.27 | |
Formula | C12H16N2O3 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Borrello MT, et al. FEBS J. 2025 Mar 14. doi: 10.1111/febs.70062.
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