1. PROTAC Epigenetics Cell Cycle/DNA Damage
  2. Ligands for Target Protein for PROTAC HDAC
  3. HDAC3-IN-8

HDAC3-IN-8 is a selective inhibitor targeting HDAC1, HDAC2 and HDAC3, with IC50 values of 3.52 nM for HDAC1, 15.14 nM for HDAC2 and 0.38 nM for HDAC3. HDAC3-IN-8 shows high selectivity for HDAC3 and exerts its effect by inhibiting histone deacetylase activity. HDAC3-IN-8 can be used to construct HDAC3-targeted PROTAC degrader (HY-181767) and is suitable for the research of acute myeloid leukemia (AML).

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

HDAC3-IN-8

HDAC3-IN-8 Chemical Structure

CAS No. : 2763368-90-5

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Description

HDAC3-IN-8 is a selective inhibitor targeting HDAC1, HDAC2 and HDAC3, with IC50 values of 3.52 nM for HDAC1, 15.14 nM for HDAC2 and 0.38 nM for HDAC3. HDAC3-IN-8 shows high selectivity for HDAC3 and exerts its effect by inhibiting histone deacetylase activity. HDAC3-IN-8 can be used to construct HDAC3-targeted PROTAC degrader (HY-181767) and is suitable for the research of acute myeloid leukemia (AML)[1].

IC50 & Target[1]

HDAC3

0.38 nM (IC50)

HDAC1

3.52 nM (IC50)

HDAC2

15.14 nM (IC50)

In Vitro

HDAC3-IN-8 (3) exhibits inhibitory activity against HDAC1, HDAC2 and HDAC3 with IC50 values of 3.52 nM, 15.14 nM and 0.38 nM, respectively[1].

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

Molecular Weight

351.40

Formula

C20H21N3O3

CAS No.
SMILES

O=C(C1=CC2=CC=CC=C2O1)NCC3=CC=C(C(NNCCC)=O)C=C3

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Product Name:
HDAC3-IN-8
Cat. No.:
HY-181768
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