Ludartin
Ludartin a sesquiterpene lactone, which can be isolated from the plant Artemisia carruthii Wood. Ludartin reduces the expression of myeloperoxidase and malondialdehyde, enhances the expression of glutathione and superoxide dismutase in spinal cord tissue. Ludartin inhibits neuronal apoptosis. Ludartin inhibits the upregulation of tumor necrosis factor-α, interleukin-1β, and interleukin-6. Ludartin improves the motor function of rats with spinal cord injury.
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- CAS No.: 36149-87-8
- Formule: C15H18O3
- Masse moléculaire:246.30
-
Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Activité biologique
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Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A-431 | IC50 |
19 μM
Compound: Ludartin
|
Cytotoxicity against human A431 cells assessed as reduction in cell viability incubated for 24 hrs by MTT assay
Cytotoxicity against human A431 cells assessed as reduction in cell viability incubated for 24 hrs by MTT assay
|
[PMID: 31784199] |
| A549 | IC50 |
25.18 μM
Compound: Ludartin
|
Antiproliferative activity against human A549 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Antiproliferative activity against human A549 cells assessed as reduction in cell viability after 48 hrs by MTT assay
|
[PMID: 31784199] |
| A549 | IC50 |
7.4 μM
Compound: 1
|
Cytotoxicity against human A549 cells assessed as cell growth inhibition after 48 hrs by sulphorhodamine B assay
Cytotoxicity against human A549 cells assessed as cell growth inhibition after 48 hrs by sulphorhodamine B assay
|
[PMID: 23886685] |
| A549 | IC50 |
7.4 μM
Compound: 1
|
Cytotoxicity against human A549 cells assessed as growth inhibition by colorimetric sulphorhodamine B assay
Cytotoxicity against human A549 cells assessed as growth inhibition by colorimetric sulphorhodamine B assay
|
[PMID: 24484897] |
| B16-F10 | IC50 |
6.6 μM
Compound: Ludartin
|
Cytotoxicity against mouse B16F10 cells assessed as reduction in cell viability incubated for 24 hrs by MTT assay
Cytotoxicity against mouse B16F10 cells assessed as reduction in cell viability incubated for 24 hrs by MTT assay
|
[PMID: 31784199] |
| BHY | IC50 |
25.18 μM
Compound: Ludartin
|
Antiproliferative activity against human BHY cells assessed as reduction in cell viability after 48 hrs by MTT assay
Antiproliferative activity against human BHY cells assessed as reduction in cell viability after 48 hrs by MTT assay
|
[PMID: 31784199] |
| COLO 205 | IC50 |
25.18 μM
Compound: Ludartin
|
Antiproliferative activity against human COLO205 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Antiproliferative activity against human COLO205 cells assessed as reduction in cell viability after 48 hrs by MTT assay
|
[PMID: 31784199] |
| HCT-116 | IC50 |
6.9 μM
Compound: 1
|
Cytotoxicity against human HCT116 cells assessed as cell growth inhibition after 48 hrs by sulphorhodamine B assay
Cytotoxicity against human HCT116 cells assessed as cell growth inhibition after 48 hrs by sulphorhodamine B assay
|
[PMID: 23886685] |
| HCT-116 | IC50 |
6.9 μM
Compound: 1
|
Cytotoxicity against human HCT116 cells assessed as growth inhibition by colorimetric sulphorhodamine B assay
Cytotoxicity against human HCT116 cells assessed as growth inhibition by colorimetric sulphorhodamine B assay
|
[PMID: 24484897] |
| MCF7 | IC50 |
0.5 μM
Compound: 1
|
Cytotoxicity against human MCF7 cells assessed as growth inhibition by colorimetric sulphorhodamine B assay
Cytotoxicity against human MCF7 cells assessed as growth inhibition by colorimetric sulphorhodamine B assay
|
[PMID: 24484897] |
| MCF7 | IC50 |
25.18 μM
Compound: Ludartin
|
Antiproliferative activity against human MCF7 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Antiproliferative activity against human MCF7 cells assessed as reduction in cell viability after 48 hrs by MTT assay
|
[PMID: 31784199] |
| MIA PaCa-2 | IC50 |
25.18 μM
Compound: Ludartin
|
Antiproliferative activity against human MIAPaCa2 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Antiproliferative activity against human MIAPaCa2 cells assessed as reduction in cell viability after 48 hrs by MTT assay
|
[PMID: 31784199] |
| PC-3 | IC50 |
7.5 μM
Compound: 1
|
Cytotoxicity against human PC3 cells assessed as cell growth inhibition after 48 hrs by sulphorhodamine B assay
Cytotoxicity against human PC3 cells assessed as cell growth inhibition after 48 hrs by sulphorhodamine B assay
|
[PMID: 23886685] |
| PC-3 | IC50 |
7.5 μM
Compound: 1
|
Cytotoxicity against human PC3 cells assessed as growth inhibition by colorimetric sulphorhodamine B assay
Cytotoxicity against human PC3 cells assessed as growth inhibition by colorimetric sulphorhodamine B assay
|
[PMID: 24484897] |
| T98G | IC50 |
6.3 μM
Compound: 1
|
Cytotoxicity against human T98G cells assessed as growth inhibition by colorimetric sulphorhodamine B assay
Cytotoxicity against human T98G cells assessed as growth inhibition by colorimetric sulphorhodamine B assay
|
[PMID: 24484897] |
| THP-1 | IC50 |
3.1 μM
Compound: 1
|
Cytotoxicity against human THP1 cells assessed as cell growth inhibition after 48 hrs by sulphorhodamine B assay
Cytotoxicity against human THP1 cells assessed as cell growth inhibition after 48 hrs by sulphorhodamine B assay
|
[PMID: 23886685] |
| THP-1 | IC50 |
3.1 μM
Compound: 1
|
Cytotoxicity against human THP1 cells assessed as growth inhibition by colorimetric sulphorhodamine B assay
Cytotoxicity against human THP1 cells assessed as growth inhibition by colorimetric sulphorhodamine B assay
|
[PMID: 24484897] |
Chemical Information
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CAS No. 36149-87-8
-
Masse moléculaire 246.30
-
Formule C15H18O3
-
SMILES
C[C@]12[C@]3([H])[C@]4([H])[C@](CCC(C)=C3C[C@@]1([H])O2)([H])C(C(O4)=O)=C
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Initial Source
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Livraison
Room temperature in continental US; may vary elsewhere.
-
Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)