Chaparrinone
Chaparrinone is a quassinoid that can be isolated from the root of Eurycoma harmandiana. Chaparrinone has antimalarial and cytotoxic activities against Plasmodium falciparum and P-388 cells (IC50: 0.037 and 0.34 μg/mL respectively).
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- CAS 番号: 22611-34-3
- 分子式: C20H26O7
- 分子量:378.42
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
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生物活性
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Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| BT-549 | IC50 |
0.8 μg/mL
Compound: chaparrinone
|
Cytotoxicity against human BT549 cells after 2 to 7 days by neutral red assay
Cytotoxicity against human BT549 cells after 2 to 7 days by neutral red assay
|
[PMID: 8984156] |
| Hep 3B2 | IC50 |
2.17 μM
Compound: 4
|
Cytotoxicity against human Hep3B cells measured after 48 hrs by MTT assay
Cytotoxicity against human Hep3B cells measured after 48 hrs by MTT assay
|
[PMID: 23290052] |
| HepG2 | IC50 |
>50 μM
Compound: 4
|
Cytotoxicity against human adriamycin-resistant HepG2 cells measured after 48 hrs by MTT assay
Cytotoxicity against human adriamycin-resistant HepG2 cells measured after 48 hrs by MTT assay
|
[PMID: 23290052] |
| HepG2 | IC50 |
1.2 μM
Compound: 4
|
Cytotoxicity against human HepG2 cells measured after 48 hrs by MTT assay
Cytotoxicity against human HepG2 cells measured after 48 hrs by MTT assay
|
[PMID: 23290052] |
| HL-60 | EC50 |
2.4 μM
Compound: 26
|
Induction of cell differentiation in human HL60 cells assessed as superoxide anion production after 4 days by NBT reduction assay
Induction of cell differentiation in human HL60 cells assessed as superoxide anion production after 4 days by NBT reduction assay
|
[PMID: 11754601] |
| HL-60 | IC50 |
1.2 μM
Compound: 26
|
Antiproliferative activity against human HL60 cells assessed as inhibition of [3H]thymidine incorporation after 4 days by liquid scintillation counter
Antiproliferative activity against human HL60 cells assessed as inhibition of [3H]thymidine incorporation after 4 days by liquid scintillation counter
|
[PMID: 11754601] |
| HL-60 | IC50 |
5 μM
Compound: 26
|
Cytotoxicity against human HL60 cells assessed as loss of membrane integrity after 4 days by trypan blue exclusion assay
Cytotoxicity against human HL60 cells assessed as loss of membrane integrity after 4 days by trypan blue exclusion assay
|
[PMID: 11754601] |
| K562 | IC50 |
1.8 μg/mL
Compound: chaparrinone
|
Cytotoxicity against human K562 cells after 2 to 7 days by neutral red assay
Cytotoxicity against human K562 cells after 2 to 7 days by neutral red assay
|
[PMID: 8984156] |
| KB | ED50 |
0.025 μg/mL
Compound: 2, NSC-288754
|
Cytotoxicity against human KB cells by NCI method
Cytotoxicity against human KB cells by NCI method
|
[PMID: 6875576] |
| KB | IC50 |
1.2 μg/mL
Compound: chaparrinone
|
Cytotoxicity against human KB cells after 2 to 7 days by neutral red assay
Cytotoxicity against human KB cells after 2 to 7 days by neutral red assay
|
[PMID: 8984156] |
| P388 | IC50 |
0.92 μg/mL
Compound: 6
|
Cytotoxicity against mouse P388 cells after 3 days by MTT assay
Cytotoxicity against mouse P388 cells after 3 days by MTT assay
|
[PMID: 9644063] |
| SK-OV-3 | IC50 |
0.5 μg/mL
Compound: chaparrinone
|
Cytotoxicity against human SKOV3 cells after 2 to 7 days by neutral red assay
Cytotoxicity against human SKOV3 cells after 2 to 7 days by neutral red assay
|
[PMID: 8984156] |
| Vero | IC50 |
1.5 μg/mL
Compound: chaparrinone
|
Cytotoxicity against african green monkey Vero cells after 2 to 7 days by neutral red assay
Cytotoxicity against african green monkey Vero cells after 2 to 7 days by neutral red assay
|
[PMID: 8984156] |
化学情報
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CAS 番号 22611-34-3
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分子量 378.42
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分子式 C20H26O7
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SMILES
C[C@@]12[C@]3([H])[C@@]45[C@@](OC(C[C@@]4([H])[C@H]([C@H]([C@@]3(OC5)O)O)C)=O)([H])C[C@@]1([H])C(C)=CC([C@H]2O)=O
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Structure Classification
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Initial Source
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
[1]. Kanchanapoom T, et al. Quassinoids from Eurycoma harmandiana. Phytochemistry. 2001 Aug;57(8):1205-8. [Content Brief]
[2]. François G, et al. Antimalarial and cytotoxic potential of four quassinoids from Hannoa chlorantha and Hannoa klaineana, and their structure-activity relationships. Int J Parasitol. 1998 Apr;28(4):635-40. [Content Brief]
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)