1. Cell Cycle/DNA Damage Epigenetics
  2. HDAC
  3. HDAC6-IN-66

HDAC6-IN-66 is a potent and selective histone deacetylase (HDAC) 6 inhibitor with an IC50 of 1.8 nM. HDAC6-IN-66 induces α-tubulin acetylation over histone H3. HDAC6-IN-66 can be used for the research of cancer.

For research use only. We do not sell to patients.

HDAC6-IN-66

HDAC6-IN-66 Chemical Structure

CAS No. : 3095060-23-1

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Description

HDAC6-IN-66 is a potent and selective histone deacetylase (HDAC) 6 inhibitor with an IC50 of 1.8 nM. HDAC6-IN-66 induces α-tubulin acetylation over histone H3. HDAC6-IN-66 can be used for the research of cancer[1].

IC50 & Target[1]

HDAC6

1.8 nM (IC50)

HDAC3

73.6 nM (IC50)

HDAC1

104.9 nM (IC50)

In Vitro

HDAC6-IN-66 (Compound 5j) selectively inhibits HDAC6 (IC50 = 1.8 nM), with significantly higher IC50 against other HDAC isoforms (HDAC1 : 104.9 nM, HDAC3 : 73.6 nM; HDAC4 : 271.3 nM)[1].
HDAC6-IN-66 exhibits significant antiproliferative activity against HCT116 cells (GI50 = 3.1 μM), and shows mild inhibitory activity against other cancer cell lines such as MDA-MB-231 (GI50 = 22.3 μM) and HCC827 cells (GI50 = 15.9 μM)[1].
HDAC6-IN-66 (0.5-10 μM, 24 h) induces acetylation of α-tubulin in HCT116 and MDA-MB-231 cells[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

333.34

Formula

C19H15N3O3

CAS No.
SMILES

O=C(NO)C1=CC=C(CN2N=C(C3=CC=CO3)C4=C2C=CC=C4)C=C1

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Room temperature in continental US; may vary elsewhere.

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Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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Product Name:
HDAC6-IN-66
Cat. No.:
HY-178333
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