HDAC6/8/BRPF1-IN-1

Modify Date: 2025-08-25 20:20:04

HDAC6/8/BRPF1-IN-1 structure	Common Name	HDAC6/8/BRPF1-IN-1
	CAS Number	2484255-65-2	Molecular Weight	387.41
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₁₈H₁₇N₃O₅S	Melting Point	N/A
	MSDS	N/A	Flash Point	N/A

Use of HDAC6/8/BRPF1-IN-1

HDAC6/8/BRPF1-IN-1 is a dual inhibitor of both HDAC6/8 and the bromodomain and PHD finger containing protein 1 (BRPF1). HDAC6/8/BRPF1-IN-1 has inhibitory activity for HDAC1, HDAC6 and HDAC8 with IC50 values of 797 nM, 344 nM and 908 nM, respectively. HDAC6/8/BRPF1-IN-1 has inhibitory activity for BRPF1 with an Kd value of 175.2 nM. HDAC6/8/BRPF1-IN-1 can be used for the research of cancer[1].

Name	HDAC6/8/BRPF1-IN-1

Description	HDAC6/8/BRPF1-IN-1 is a dual inhibitor of both HDAC6/8 and the bromodomain and PHD finger containing protein 1 (BRPF1). HDAC6/8/BRPF1-IN-1 has inhibitory activity for HDAC1, HDAC6 and HDAC8 with IC50 values of 797 nM, 344 nM and 908 nM, respectively. HDAC6/8/BRPF1-IN-1 has inhibitory activity for BRPF1 with an Kd value of 175.2 nM. HDAC6/8/BRPF1-IN-1 can be used for the research of cancer[1].
Related Catalog	Research Areas >> Cancer Signaling Pathways >> Cell Cycle/DNA Damage >> HDAC Signaling Pathways >> Epigenetics >> HDAC
Target	HDAC1:797 nM (IC50) HDAC6:344 nM (IC50) HDAC8:908 nM (IC50)
In Vitro	HDAC6/8/BRPF1-IN-1 has inhibitory activity for HDAC1, HDAC6 and HDAC8 with IC50 values of 797 nM, 344 nM and 908 nM, respectively[1]. HDAC6/8/BRPF1-IN-1 has inhibitory activity for BRPF1 with an Kd value of 175.2 nM[1].
References	[1]. Ehab Ghazy, et al. Design, synthesis, and biological evaluation of dual targeting inhibitors of histone deacetylase 6/8 and bromodomain BRPF1. Eur J Med Chem. 2020 Aug 15;200:112338.

Molecular Formula	C₁₈H₁₇N₃O₅S
Molecular Weight	387.41

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HDAC6/8/BRPF1-IN-1

Use of HDAC6/8/BRPF1-IN-1

Names

HDAC6/8/BRPF1-IN-1 Biological Activity

Chemical & Physical Properties

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.