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BG45

Catalog No. T2294   CAS 926259-99-6

BG45 is an HDAC I type inhibitor with IC50 of 289 nM, 2.0 μM, 2.2 μM and <20 μM for HDAC3/1/2/6 in cell-free assays, respectively.

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BG45 Chemical Structure
BG45, CAS 926259-99-6
Pack Size Availability Price/USD Quantity
2 mg In stock $ 35.00
5 mg In stock $ 57.00
10 mg In stock $ 97.00
25 mg In stock $ 176.00
50 mg In stock $ 297.00
100 mg In stock $ 477.00
200 mg In stock $ 612.00
1 mL * 10 mM (in DMSO) In stock $ 63.00
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Purity: 99.91%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description BG45 is an HDAC I type inhibitor with IC50 of 289 nM, 2.0 μM, 2.2 μM and >20 μM for HDAC3/1/2/6 in cell-free assays, respectively.
Targets&IC50 HDAC1:2 μM, HDAC3:289 nM, HDAC2:2.2 μM
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]
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]
Kinase Assay Kinase assays: Initial rate constants are measured at 21 °C in the presence of 100 mM HEPES (pH 7.5), 0.3 mg/mL poly(Glu-Tyr) peptide substrate, 10 mM MgCl2, 1 mg/mL bovine serum albumin, 5% DMSO, 20 nM MET-KD and various concentrations of ATP and SGX523. Total reaction volumes (20 μL) are quenched with 20 μL Kinase-Glo detection buffer. Luminescence is detected in a plate-reading luminometer and the results are analyzed by nonlinear regression.
Cell Research 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.(Only for Reference)
Molecular Weight 214.22
Formula C11H10N4O
CAS No. 926259-99-6

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

Ethanol: 2 mg/mL (9.33 mM), Heating is recommended.

DMSO: 39 mg/mL (182.1 mM)

H2O: < 1 mg/mL (insoluble or slightly soluble)

TargetMolReferences and Literature

1. Minami J, et al. Leukemia. 2014, 28(3), 680-689.

Related compound libraries

This product is contained In the following compound libraries:
Inhibitor Library Chromatin Modification Compound Library Reprogramming Compound Library Anti-Breast Cancer Compound Library Apoptosis Compound Library Histone Modification Compound Library HIF-1 Signaling Pathway Compound Library Anti-Cancer Compound Library Bioactive Compounds Library Max Hematonosis Compound Library

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Keywords

BG45 926259-99-6 Apoptosis Chromatin/Epigenetic DNA Damage/DNA Repair HDAC Inhibitor inhibit Histone deacetylases BG 45 BG-45 inhibitor

 

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