1. Metabolic Enzyme/Protease NF-κB Immunology/Inflammation MAPK/ERK Pathway Stem Cell/Wnt
  2. Tyrosinase NF-κB AP-1 Interleukin Related p38 MAPK JNK ERK
  3. Norkurarinol

Norkurarinol is a prenylated flavonoid. Norkurarinol can be isolated from Sophora flavescens. Norkurarinol potently inhibits mushroom Tyrosinase DOPA oxidase activity with an IC50 of 2.1 μM. Norkurarinol inhibits poly(I:C)-induced NF-κB/AP-1 activation. Norkurarinol inhibits pro-inflammatory cytokines (TNF-α, IL-6). Norkurarinol inhibits phosphorylation of p38, JNK, and ERK1/2. Norkurarinol increases phosphorylation of IRF3. Norkurarinol has antiviral activity against Rotavirus KJ56-1

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Norkurarinol

Norkurarinol Chemical Structure

CAS No. : 52483-01-9

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Description

Norkurarinol is a prenylated flavonoid. Norkurarinol can be isolated from Sophora flavescens. Norkurarinol potently inhibits mushroom Tyrosinase DOPA oxidase activity with an IC50 of 2.1 μM. Norkurarinol inhibits poly(I:C)-induced NF-κB/AP-1 activation. Norkurarinol inhibits pro-inflammatory cytokines (TNF-α, IL-6). Norkurarinol inhibits phosphorylation of p38, JNK, and ERK1/2. Norkurarinol increases phosphorylation of IRF3. Norkurarinol has antiviral activity against Rotavirus KJ56-1[1][2]

IC50 & Target[1]

p38

 

ERK1

 

ERK2

 

IL-6

 

mushroom Tyrosinase

2.1 μM (IC50)

In Vitro

Norkurarinol (10-30 μM; 18 h total with poly(I:C)) inhibits poly(I:C)-induced NF-κB/AP-1 activation in THP1-Blue-CD14 cells with an IC50 of 20.9 μM[1].
Norkurarinol (30 μM) suppresses rotavirus-induced mRNA expression of pro-inflammatory cytokines (TNF-α, IL-6) in TF-104 cells[1].
Norkurarinol (10-60 μM; 2-6 h for THP-1, 24 h for TF-104) induces IRF3 phosphorylation and IFNβ mRNA expression in THP-1 cells, enhances poly(I:C)-induced IFNβ expression in THP-1 cells, and increases rotavirus-induced IFNβ expression in TF-104 cells[1].
Norkurarinol (30 μM; 72 h during rotavirus infection) inhibits rotavirus KJ56-1 replication in TF-104 cells, reducing viral titer by over 5 logs[1].
Norkurarinol (0.1-100 μM; 20 min) potently inhibits mushroom tyrosinase DOPA oxidase activity with an IC50 of 2.1 μM[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[1]

Cell Line: THP-1 cells
Concentration: 10-60 μM
Incubation Time: 2 h (with poly(I:C))
Result: Inhibited poly(I:C)-induced nuclear translocation of NF-κB p65 and AP-1 subunit c-fos in a dose-dependent manner.
Inhibited poly(I:C)-induced phosphorylation of IκB, IKKα/β, IKKγ, p38, JNK, and ERK1/2 in a dose-dependent manner.
Increased poly(I:C)-induced phosphorylation of IRF3 in a dose-dependent manner.
Molecular Weight

442.50

Formula

C25H30O7

CAS No.
SMILES

CC(C)(O)CC[C@@H](C(C)=C)CC1=C2C(C(C[C@@H](C3=C(C=C(C=C3)O)O)O2)=O)=C(C=C1O)O

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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