Bobcat339 hydrochloride

Synonyms: Bobcat339 HCl

Bobcat339 is a selective cytosine-based TET enzyme inhibitor with IC50 of 33 μM and 73 μM for TET1 and TET2, respectively. Bobcat339 can reduce DNA 5-hydroxymethylcytosine abundance by inhibiting TET enzyme function in living cells and provide support for its utility as a viable pharmacological probe.

Bobcat339 hydrochloride Chemical Structure

Bobcat339 hydrochloride Chemical Structure

CAS: 2436747-44-1

Selleck's Bobcat339 hydrochloride has been cited by 5 publications

Purity & Quality Control

Batch: Purity: 99.59%
99.59

Bobcat339 hydrochloride Related Products

Choose Selective DNA Methyltransferase Inhibitors

Biological Activity

Description Bobcat339 is a selective cytosine-based TET enzyme inhibitor with IC50 of 33 μM and 73 μM for TET1 and TET2, respectively. Bobcat339 can reduce DNA 5-hydroxymethylcytosine abundance by inhibiting TET enzyme function in living cells and provide support for its utility as a viable pharmacological probe.
Targets
TET1 [1]
(Cell-free assay)
TET2 [1]
(Cell-free assay)
33 μM 73 μM
In vitro
In vitro

Bobcat339, the TET2 enzyme activity inhibitor, decreases the TET2 enzyme activity and protects cells from neurotoxin damage in SH-SY5Y cells.[2]

Cell Research Cell lines SH-SY5Y neuroblastoma cells
Concentrations 3 μM
Incubation Time 12 h
Method

The CCK-8 assay kit was used to determine cell viability. SH-SY5Y cells are seeded into 96-well plates at a density of 5,000 cells/well with 100 μl of cell medium in each well. Bobcat339 (3 μM) is preincubated with cells for 12 h before MPP+ (2.5 mM) treatment. Then, 10 μl of CCK-8 working solution is added to each well to incubate for about 1 h at 37 C. The wells containing only the culture medium served as blanks. The absorbance value at 450 nm is measured.

In Vivo
In vivo

Bobcat339 hydrochloride is a potent and selective cytosine-based inhibitor of TET enzyme.

Chemical Information & Solubility

Molecular Weight 334.2 Formula

C16H13Cl2N3O

CAS No. 2436747-44-1 SDF --
Smiles C1=CC=C(C=C1)C2=CC(=CC=C2)N3C=C(C(=NC3=O)N)Cl
Storage (From the date of receipt) 3 years -20°C powder

In vitro
Batch:

DMSO : 60 mg/mL ( (179.53 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Ethanol : 1 mg/mL

Water : Insoluble


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In vivo
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

Handling Instructions

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