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AB141640

BML-210, HDAC inhibitor

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(1 Publication)

MW 339.4 Da, Purity >98%. Histone deacetylase (HDAC) inhibitor (IC50 = 87 μM). Induces changes in gene expression profile. Antiproliferative activity in vitro.
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Chemical Structure - BML-210, HDAC inhibitor (AB141640)
  • Chemical Structure

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Chemical Structure - BML-210, HDAC inhibitor (AB141640)

2D chemical structure image of ab141640, BML-210, HDAC inhibitor

Key facts

CAS number

537034-17-6

Purity

>98%

Form

Solid

form

Molecular weight

339.4 Da

Molecular formula

C<sub>2</sub><sub>0</sub>H<sub>2</sub><sub>5</sub>N<sub>3</sub>O<sub>2</sub>

PubChem

9543540

Nature

Synthetic

Solubility

Soluble in DMSO to 50 mM

Soluble in ethanol to 25 mM (with warming)

Biochemical name

N1-(2-aminophenyl)-N8-phenyloctanediamide

Biological description

Histone deacetylase (HDAC) inhibitor (IC50 = 87 μM). Induces changes in gene expression profile. Antiproliferative activity in vitro.

Canonical smiles

C1=CC=C(C=C1)NC(=O)CCCCCCC(=O)NC2=CC=CC=C2N

InChi

InChI=1S/C20H25N3O2/c21-17-12-8-9-13-18(17)23-20(25)15-7-2-1-6-14-19(24)22-16-10-4-3-5-11-16/h3-5,8-13H,1-2,6-7,14-15,21H2,(H,22,24)(H,23,25)

InChiKey

RFLHBLWLFUFFDZ-UHFFFAOYSA-N

IUPAC Name

N'-(2-aminophenyl)-N-phenyloctanediamide

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Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
Store under desiccating conditions|The product can be stored for up to 12 months
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Product protocols

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Publications (1)

Recent publications for all applications. Explore the full list and refine your search

Nature communications 7:10606 PubMed26842135

2016

Activating frataxin expression by repeat-targeted nucleic acids.

Applications

Unspecified application

Species

Unspecified reactive species

Liande Li,Masayuki Matsui,David R Corey
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