1. PI3K/Akt/mTOR NF-κB Immunology/Inflammation Apoptosis
  2. PTEN Akt NF-κB Interleukin Related TNF Receptor
  3. Coelonin

Coelonin is a dihydrophenanthrene with anti-inflammation activity. Coelonin inhibits LPS-induced PTEN phosphorylation. Coelonin inhibits NF-κB activation and p27Kip1 degradation by regulating the PI3K/AKT pathway negatively. Coelonin can inhibit IκBα phosphorylation and degradation and increases the expression of IκBα protein.

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Coelonin Chemical Structure

Coelonin Chemical Structure

CAS No. : 82344-82-9

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Based on 1 publication(s) in Google Scholar

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Description

Coelonin is a dihydrophenanthrene with anti-inflammation activity. Coelonin inhibits LPS-induced PTEN phosphorylation. Coelonin inhibits NF-κB activation and p27Kip1 degradation by regulating the PI3K/AKT pathway negatively. Coelonin can inhibit IκBα phosphorylation and degradation and increases the expression of IκBα protein[1][2].

IC50 & Target

Akt

 

NF-κB

 

IL-1β

 

IL-6

 

Cellular Effect
Cell Line Type Value Description References
A549 EC50
5.05 μg/mL
Compound: 10
Cytotoxicity against human A549 cells after 3 days by sulforhodamine B assay
Cytotoxicity against human A549 cells after 3 days by sulforhodamine B assay
[PMID: 19193043]
BV-2 IC50
15.2 μM
Compound: 16
Antineuroinflammatory activity against mouse BV2 cells assessed as inhibition of LPS-induced NO production incubated for 24 hrs by Griess assay
Antineuroinflammatory activity against mouse BV2 cells assessed as inhibition of LPS-induced NO production incubated for 24 hrs by Griess assay
[PMID: 31415170]
DU-145 EC50
4.79 μg/mL
Compound: 10
Cytotoxicity against human DU145 cells after 3 days by sulforhodamine B assay
Cytotoxicity against human DU145 cells after 3 days by sulforhodamine B assay
[PMID: 19193043]
HCT-8 EC50
3.84 μg/mL
Compound: 10
Cytotoxicity against human HCT8 cells after 3 days by sulforhodamine B assay
Cytotoxicity against human HCT8 cells after 3 days by sulforhodamine B assay
[PMID: 19193043]
KB EC50
3.4 μg/mL
Compound: 10
Cytotoxicity against human KB cells after 3 days by sulforhodamine B assay
Cytotoxicity against human KB cells after 3 days by sulforhodamine B assay
[PMID: 19193043]
MCF7 EC50
1.8 μg/mL
Compound: 10
Cytotoxicity against human MCF7 cells after 3 days by sulforhodamine B assay
Cytotoxicity against human MCF7 cells after 3 days by sulforhodamine B assay
[PMID: 19193043]
Neutrophil IC50
> 10 μM
Compound: 15
Antiinflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced elastase release using MeO-Suc-Ala-Ala-Pro-Val-p-nitroanilide as elastase substrate preincubated for 5 mins followed by fMLP/CB-induction
Antiinflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced elastase release using MeO-Suc-Ala-Ala-Pro-Val-p-nitroanilide as elastase substrate preincubated for 5 mins followed by fMLP/CB-induction
[PMID: 27525452]
Neutrophil IC50
0.4 μM
Compound: 15
Antiinflammatory activity in human neutrophils assessed as inhibition of FMLP/cytochalasin B-induced superoxide anion generation by measuring superoxide dismutase-inhibitable reduction of ferricytochrome c preincubated for 5 mins followed by FMLP/cytochal
Antiinflammatory activity in human neutrophils assessed as inhibition of FMLP/cytochalasin B-induced superoxide anion generation by measuring superoxide dismutase-inhibitable reduction of ferricytochrome c preincubated for 5 mins followed by FMLP/cytochal
[PMID: 27525452]
PC-3 EC50
2.82 μg/mL
Compound: 10
Cytotoxicity against human PC3 cells after 3 days by sulforhodamine B assay
Cytotoxicity against human PC3 cells after 3 days by sulforhodamine B assay
[PMID: 19193043]
In Vitro

Coelonin (2.5 μg/mL) significantly reduces both NF-κB p65 and p105/50 phosphorylation levels[1].
Coelonin (0-5 μg/mL, 1.5 h) dose dependently reduces the increase of the phosphorylation of PTEN, AKT and IκBa induced by LPS[1].
Coelonin (10 and 20 μg/ml) mitigates particulate matter 2.5 (PM2.5)-induced inflammation by reducing the generation of inflammatory factors, including interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α)[2].
The inhibition of IL-1β, IL-6 and TNF-α expression by Coelonin is independent of PTEN, whereas the inhibition of p27Kip1 degradation results in cell-cycle arrest in the G1 phase, which is dependent on PTEN[1].

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

Molecular Weight

242.27

Formula

C15H14O3

CAS No.
SMILES

OC(C=C1CC2)=CC(OC)=C1C3=C2C=C(O)C=C3

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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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
Coelonin
Cat. No.:
HY-N8884
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