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JSH-23

SKU: orb1307077

Description

JSH-23 is a cell-permeable inhibitor that selectively blocks NF-κB-dependent transcriptional activity (IC50=7.1 µM) without preventing IκBα degradation. This antioxidant compound is used in vitro and in vivo to study inflammatory signaling pathways and oxidative stress-related mechanisms.

Research Area

Signal Transduction

Images & Validation

Key Properties

CAS Number749886-87-1
MW240.34
Purity99.67% (May vary between batches)
FormulaC16H20N2
SMILESCc1ccc(NCCCc2ccccc2)c(N)c1
TargetNF-κB
SolubilityH2O:< 1 mg/mL (insoluble or slightly soluble);10% DMSO+40% PEG300+5% Tween 80+45% Saline:5 mg/mL (20.8 mM);Ethanol:16 mg/mL (66.57 mM);DMSO:255 mg/mL (1061 mM)

Bioactivity

Target IC50
NF-κB (RAW 264.7 cells):7.1 μM|U-87MG cells:59.39 μM|U251MG cells:56.21μM|NF-κB:7.1 μM
In Vivo
METHODS: To investigate the role in diabetic neuropathy, JSH-23 (1-3 mg/kg) was administered orally to streptozotocin-induced diabetic rats once daily for two weeks. RESULTS: JSH-23 treatment significantly reversed nerve conduction and nerve blood flow deficits in diabetic animals. The treatment also partially corrected the reduced mechanical pain threshold.JSH-23 treatment inhibited nuclear translocation of the p65/p50 subunit in the sciatic nerve.
In Vitro
METHODS: Bone marrow macrophage BMMs were treated with JSH-23 (0.78-200 µM) for 48-96 h. Cell viability was measured by CCK-8 assay. RESULTS: JSH-23 had no detectable toxic effects at concentrations below 50 µM. METHODS: Macrophages RAW 264.7 harboring the reporter gene pNF-κB-SEAP-NPT were treated with LPS (1 µg/mL) and JSH-23 (1-30 µM) for 16 days, and SEAP expression was assayed to reflect NF-κB transcriptional activity. RESULTS: JSH-23 inhibited LPS-induced SEAP expression in a dose-dependent manner by 23±3% at 3 µM, 68±3% at 10 µM, and 103±4% at 30 µM. JSH-23 inhibited NF-κB transcriptional activity.
Cell Research
Macrophages RAW 264.7 are incubated with various concentrations of JSH-23 compound for 24 h. The cells are treated with WST-1 solution and absorbance is measured at 450 nm.(Only for Reference)

Storage & Handling

Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

Inhibitor, JSH 23, JSH23, JSH-23, inhibit, NF-κB, NFκB, NFkB, NF-kB, Nuclear factor-κB, Nuclear factor-kappaB

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  • JSH-23 [orb1224075]

    >98% (HPLC)

    749886-87-1

    240.34

    C16H20N2

    1 g, 500 mg, 200 mg, 100 mg, 2 mg, 5 mg, 25 mg, 50 mg, 10 mg
Quality Guarantee

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Key Properties

No computed properties available.

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Protocol Information

JSH-23 (orb1307077)

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

Select a size below

1 mg
$ 80.00
2 mg
$ 100.00
5 mg
$ 130.00
1 ml x 10 mM (in DMSO)
$ 140.00
10 mg
$ 170.00
25 mg
$ 240.00
50 mg
$ 340.00
100 mg
$ 500.00
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