Home DNA Damage/DNA Repair HDAC inhibitor BG45 For research use only.

BG45

BG45 is a class I HDAC inhibitor with IC50 of 289 nM, 2.0 µM, 2.2 µM and >20 µM for HDAC3, HDAC1, HDAC2, and HDAC6 in cell-free assays, respectively.

BG45 Chemical Structure

BG45 Chemical Structure

CAS: 926259-99-6

Selleck's BG45 has been cited by 6 publications

Purity & Quality Control

Batch: Purity: 99.96%
99.96

BG45 Related Products

Signaling Pathway

HDAC Signaling Pathways

HDAC Signaling Pathway

Choose Selective HDAC Inhibitors

Biological Activity

Description BG45 is a class I HDAC inhibitor with IC50 of 289 nM, 2.0 µM, 2.2 µM and >20 µM for HDAC3, HDAC1, HDAC2, and HDAC6 in cell-free assays, respectively.
Targets
HDAC3 [1] HDAC1 [1] HDAC2 [1]
289 nM 2 μM 2.2 μM
In vitro
In vitro BG45 causes significant cell growth inhibition and induces caspase-dependent apoptosis in a series of MM cells. In RPMI8226 cells, BG45 synergistically enhances bortezomib-induced cytotoxicity. [1]
Cell Research Cell lines MM.1S, RPMI8226, U266, H929, MM.1 R, RPMI-LR5, OPM1, OPM2 and RPMI-DOX40 cells
Concentrations ~30 μM
Incubation Time 48 h
Method The growth inhibitory effects of BG45 in MM cell lines are assessed by measuring 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrasodium bromide (MTT) dye absorbance. To measure proliferation of MM cells, the rate of DNA synthesis is measured by [3H]thymidine uptake.
In Vivo
In vivo In mice bearing MM.1S xenograft of human MM, BG45 (50 mg/kg, i.p.) significantly inhibits MM tumor growth. When in combination with bortezomib, BG45 (50 mg/kg, i.p.) enhances bortezomib-induced cytotoxicity. [1]
Animal Research Animal Models Mice bearing MM.1S xenograft
Dosages 50 mg/kg, 5 days a week
Administration i.p.

Chemical Information & Solubility

Molecular Weight 214.22 Formula

C11H10N4O
CAS No. 926259-99-6 SDF Download BG45 SDF
Smiles C1=CC=C(C(=C1)N)NC(=O)C2=NC=CN=C2
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 42 mg/mL ( (196.06 mM)； Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Ethanol : 2 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.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
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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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