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HPOB

Catalog No. T2430Cas No. 1429651-50-2

HPOB is an effective and specific HDAC6 inhibitor (IC50: 56 nM), >30-fold selectivity over other HDACs.

HPOB

HPOB

Purity: 99.19%
Catalog No. T2430Cas No. 1429651-50-2
HPOB is an effective and specific HDAC6 inhibitor (IC50: 56 nM), >30-fold selectivity over other HDACs.
Pack SizePriceAvailabilityQuantity
5 mg$50In Stock
10 mg$72In Stock
1 mL x 10 mM (in DMSO)$55In Stock
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Purity:99.19%
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Product Introduction

Bioactivity
Description
HPOB is an effective and specific HDAC6 inhibitor (IC50: 56 nM), >30-fold selectivity over other HDACs.
Targets&IC50
HDAC6:56 nM
In vitro
In mice bearing CWR22 human prostate cancer xenografts, the combination of HPOB (300 mg/kg/day) with SAHA significantly inhibits the growth of pre-existing tumors, whereas the use of either compound alone does not exhibit a noticeable inhibitory effect.
In vivo
In HFS cells, HPOB enhances transformation cell death induced by Etoposide, Doxorubicin, or SAHA. HPOB also augments Etoposide-induced transformation cell death in transformed cells via the apoptosis pathway. In both normal (HFS) and transformed (LNCaP, A549, and U87) cells, HPOB induces α-tubulin proteins without affecting histones, inhibiting cell growth without impacting cell viability.
Kinase Assay
In Vitro Enzymatic Assay for Histone Deacetylases: In vitro activities of the 11 recombinant human zinc-dependent HDAC enzymes are detected by ?uorigenic release of 7-amino-4-methylcoumarin from substrate upon deacetylase enzymatic activity. A series of dilutions of the unique HDAC6 compound, tubacin, and SAHA are prepared with 10% DMSO in HDAC assay buffer, and 5 μL of the dilution was added to a 50-μL reaction so that the ?nal concentration of DMSO is 1% in all of the reactions. The enzymatic reactions are conducted in duplicate at 37 °C for 30 min in a 50-μL mixture containing HDAC assay buffer, 5 μg BSA, an HDAC substrate, an HDAC enzyme, and a test compound. After enzymatic reactions, 50 μL of 2× HDAC developer is added to each well, and the plate is incubated at room temperature for an additional 15 min. Fluorescence intensity is measured at an excitation of 360 nm and an emission of 460 nm using a Synergy microplate reader. Negative (no enzyme, no inhibitor, a drug with no HDAC inhibition activity) and positive controls (known HDAC inhibitor SAHA) are included in the assays. IC50 is determined at the drug concentration that results in 50% reduction of HDAC activity compared with the control.
Cell Research
Normal (HFS) and transformed (LNCaP, A549, and U87) cells are cultured with indicated doses of HPOB for 72 h. Five micromolars SAHA is a positive control.Graphs were constructed using Prism 5. (Only for Reference)
Chemical Properties
Molecular Weight314.34
FormulaC17H18N2O4
Cas No.1429651-50-2
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
Ethanol: 36 mg/mL (114.5 mM)
DMSO: 58 mg/mL (184.5 mM)
H2O: < 1 mg/mL (insoluble or slightly soluble)
Solution Preparation Table
Ethanol/DMSO
1mg5mg10mg50mg
1 mM3.1813 mL15.9063 mL31.8127 mL159.0634 mL
5 mM0.6363 mL3.1813 mL6.3625 mL31.8127 mL
10 mM0.3181 mL1.5906 mL3.1813 mL15.9063 mL
20 mM0.1591 mL0.7953 mL1.5906 mL7.9532 mL
50 mM0.0636 mL0.3181 mL0.6363 mL3.1813 mL
100 mM0.0318 mL0.1591 mL0.3181 mL1.5906 mL

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