Amorphispironone
Amorphispironone (Compound 1) is a rotenoid that can be isolated the leaves of A. fruticosa. Amorphispironone exhibits remarkable inhibitory effects on EBV-EA activation induced by TPA. Amorphispironone exhibits potent anti-tumor-promotion activity on mouse skin tumor promotion in vivo.
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- CAS No.: 139006-28-3
- 화학식: C23H22O7
- 분자량:410.42
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
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Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| HeLa | IC50 |
7.39 μM
Compound: 4
|
Inhibition of TNF-alpha-induced NF-kappaB activation in human HeLa cells by SEAP reporter gene assay
Inhibition of TNF-alpha-induced NF-kappaB activation in human HeLa cells by SEAP reporter gene assay
|
[PMID: 18841906] |
| KB | ED50 |
0.58 μg/mL
Compound: 4
|
Cytotoxicity against human KB cells
Cytotoxicity against human KB cells
|
[PMID: 8326318] |
| RAW264.7 | IC50 |
13.9 μM
Compound: 4
|
Inhibition of LPS-induced NF-kappaB activation in mouse RAW264.7 cells by SEAP reporter gene assay
Inhibition of LPS-induced NF-kappaB activation in mouse RAW264.7 cells by SEAP reporter gene assay
|
[PMID: 18841906] |
| RPMI-7951 | ED50 |
0.61 μg/mL
Compound: 4
|
Cytotoxicity against human RPMI7951 cells
Cytotoxicity against human RPMI7951 cells
|
[PMID: 8326318] |
Chemical Information
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CAS No. 139006-28-3
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분자량 410.42
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화학식 C23H22O7
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SMILES
CC(O1)(C)C=CC2=C1C=CC3=C2O[C@@]4([H])[C@@]([C@@](C5=O)(C=C(OC)C(OC)=C5)OC4)([H])C3=O
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Structure Classification
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Initial Source
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Please store the product under the recommended conditions in the Certificate of Analysis.
순도&문서
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)