Xerophilusin B
Xerophilusin B, an anticancer agent isolated from Isodon xerophilus, exhibits antiproliferative effects on esophageal squamous cell carcinoma (ESCC) cell lines, induces G2/M cell cycle arrest, and mediates apoptosis.
For research use only. We do not sell to patients.
- CAS No.: 167894-15-7
- Formula: C20H26O5
- Molecular Weight:346.42
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A549 | IC50 |
2 μM
Compound: 21
|
Cytotoxicity against human A549 cells after 48 hrs by MTT method
Cytotoxicity against human A549 cells after 48 hrs by MTT method
|
[PMID: 21534539] |
| HepG2 | IC50 |
3.9 μM
Compound: 27
|
Cytotoxicity against human HepG2 cells after 48 hrs
Cytotoxicity against human HepG2 cells after 48 hrs
|
[PMID: 17665952] |
| HL-60 | IC50 |
0.29 μg/mL
Compound: 2, xerophilusin B
|
Cytotoxicity against human HL60 cells after 48 hrs by MTT assay
Cytotoxicity against human HL60 cells after 48 hrs by MTT assay
|
[PMID: 10843567] |
| HL-60 | IC50 |
0.8 μM
Compound: 21
|
Cytotoxicity against human HL60 cells after 48 hrs by MTT method
Cytotoxicity against human HL60 cells after 48 hrs by MTT method
|
[PMID: 21534539] |
| K562 | IC50 |
0.73 μg/mL
Compound: 2, xerophilusin B
|
Cytotoxicity against human K562 cells after 48 hrs by MTT assay
Cytotoxicity against human K562 cells after 48 hrs by MTT assay
|
[PMID: 10843567] |
| K562 | IC50 |
4.1 μM
Compound: 27
|
Cytotoxicity against human K562 cells after 48 hrs
Cytotoxicity against human K562 cells after 48 hrs
|
[PMID: 17665952] |
| MCF7 | IC50 |
1.1 μM
Compound: 21
|
Cytotoxicity against human MCF7 cells after 48 hrs by MTT method
Cytotoxicity against human MCF7 cells after 48 hrs by MTT method
|
[PMID: 21534539] |
| MKN-28 | IC50 |
0.17 μg/mL
Compound: 2, xerophilusin B
|
Cytotoxicity against human MKN28 cells after 48 hrs by MTT assay
Cytotoxicity against human MKN28 cells after 48 hrs by MTT assay
|
[PMID: 10843567] |
| MKN-45 | IC50 |
0.4 μM
Compound: 27
|
Cytotoxicity against human MKN45 cells after 48 hrs
Cytotoxicity against human MKN45 cells after 48 hrs
|
[PMID: 17665952] |
| RAW264.7 | IC50 |
0.225 μM
Compound: 2
|
Antiinflammatory activity against mouse RAW264.7 cells assessed as inhibition of LPS-induced nitrite accumulation after 24 hrs by Griess reagent method
Antiinflammatory activity against mouse RAW264.7 cells assessed as inhibition of LPS-induced nitrite accumulation after 24 hrs by Griess reagent method
|
[PMID: 19719246] |
| RAW264.7 | IC50 |
0.7 μM
Compound: 2
|
Inhibition of NF-kappaB activation in LPS-stimulated mouse RAW264.7 cells assessed as relative luciferase activity after 24 hrs by dual reporter gene assay
Inhibition of NF-kappaB activation in LPS-stimulated mouse RAW264.7 cells assessed as relative luciferase activity after 24 hrs by dual reporter gene assay
|
[PMID: 19719246] |
| RAW264.7 | IC50 |
10.1 μM
Compound: 2
|
Cytotoxicity against mouse RAW264.7 cells after 24 hrs by MTT assay
Cytotoxicity against mouse RAW264.7 cells after 24 hrs by MTT assay
|
[PMID: 19719246] |
| SMMC-7721 | IC50 |
1.3 μM
Compound: 21
|
Cytotoxicity against human SMMC7721 cells after 48 hrs by MTT method
Cytotoxicity against human SMMC7721 cells after 48 hrs by MTT method
|
[PMID: 21534539] |
| SW480 | IC50 |
0.9 μM
Compound: 21
|
Cytotoxicity against human SW480 cells after 48 hrs by MTT method
Cytotoxicity against human SW480 cells after 48 hrs by MTT method
|
[PMID: 21534539] |
Chemical Information
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CAS No. 167894-15-7
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Molecular Weight 346.42
-
Formula C20H26O5
-
SMILES
O[C@]12[C@]34[C@]5([H])[C@@]6(C(O[C@@]3([H])[C@](CC5)([H])C(C4=O)=C)([H])O2)[C@](C(C)(CCC6)C)([H])[C@@H]1O
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Structure Classification
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Initial Source
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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
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)