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Aurantiamide

SKU: orb1301466

Description

Aurantiamide exhibits anti-cancer, anti-inflammatory, and antinociceptive properties. Its mechanisms include blocking autophagic flux to suppress glioma growth and inhibiting NF-κB, JNK, and p38 pathways to counteract neuroinflammation. This small molecule is a useful research tool for neuroscience and oncology studies in both in vitro and in vivo models.

Research Area

Cell Biology, Signal Transduction

Images & Validation

Key Properties

CAS Number58115-31-4
MW402.49
Purity98.88%
FormulaC25H26N2O3
SMILESOC[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)c1ccccc1
TargetNF-κB,p38 MAPK,RIP kinase,MLK
Solubility10% DMSO+40% PEG300+5% Tween 80+45% Saline:3.3 mg/mL (8.2 mM);DMSO:100 mg/mL (248.45 mM)

Bioactivity

In Vitro
Aurantiamide was shown to block the activation of nuclear factor-kappa B (NF-κB) in lipopolysaccharide (LPS)-induced BV2 microglial cells by inhibiting the phosphorylation of the inhibitor kappa B-α (IκB)-α. Aurantiamide decreased the phosphorylation levels of c-Jun N-terminal kinase (JNK) and p38 mitogen-activated protein kinases (MAPKs).Suggested that aurantiamide has an anti-neuroinflammatory effect on LPS stimulation through its inhibition of the NF-κB, JNK and p38 pathways.Aurantiamide has potent anti-viral and anti-inflammatory effects on IAV-infected cells via inhibition of the NF-κB pathway. Therefore ,Aurantiamide could be a potential therapeutic agent for the treatment of influenza.
Cell Research
The anti-viral activity of aurantiamide against Influenza A virus (IAV) was determined using the cytopathic effect (CPE) inhibition assay. Viruses were titrated on Madin-Darby canine kidney (MDCK) cells by plaque assays. Ribonucleoprotein (RNP) luciferase reporter assay was further conducted to investigate the effect of aurantiamide on the activity of the viral polymerase complex. HEK293T cells with a stably transfected NF-κB luciferase reporter plasmid were employed to examine the activity of aurantiamide on NF-κB activation. Activation of the host signaling pathway induced by IAV infection in the absence or presence of aurantiamide was assessed by western blotting. The effect of aurantiamide on IAV-induced expression of pro-inflammatory cytokines was measured by real-time quantitative PCR and Luminex assays.

Storage & Handling

Storagekeep away from direct sunlight | 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

p38 MAPK, p38, p38MAPK, TMC-58B, NFκB, NF-kB, NFkB, NF-κB, Inhibitor, inhibit, antioxidant, anti-inflammatory, antiplatelet, antitumor, Aurantiamide

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Quality Guarantee

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Key Properties

No computed properties available.

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Aurantiamide (orb1301466)

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

Select a size below

1 mg
$ 180.00
5 mg
$ 390.00
1 ml x 10 mM (in DMSO)
$ 540.00
10 mg
$ 560.00
25 mg
$ 870.00
50 mg
$ 1,130.00
100 mg
$ 1,530.00
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