Stypodiol
Stypodiol is an orally active sesquiterpenoid that can be isolated from Stypopodium flabelliforme. Stypodiol exhibits anticancer, gastric mucosal protective, and weak antibacterial activities. Stypodiol is used in research related to colon adenocarcinoma, neuroblastoma, basophilic leukemia, macrophage carcinoma, and gastric mucosal injury.
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: 71106-25-7
- 分子式: C27H40O4
- 分子量:428.60
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
Endogenous Metabolite アイソフォーム固有の製品をすべて表示
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生物活性
製品説明
Cellular Effect
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Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| AGS | IC50 |
153 μM
|
Cytotoxicity against human epithelial gastric AGS cells assessed as reduction in cell viability incubated for 48 h by MTT assay.
Cytotoxicity against human epithelial gastric AGS cells assessed as reduction in cell viability incubated for 48 h by MTT assay.
|
25830679 |
| Fibroblast | IC50 |
215 μM
|
Cytotoxicity against human fibroblasts assessed as reduction in cell viability incubated for 48 h by MTT assay.
Cytotoxicity against human fibroblasts assessed as reduction in cell viability incubated for 48 h by MTT assay.
|
25830679 |
体外実験
Stypodiol (12.5-50 μM; 48 h) selectively and concentration-dependently inhibits the proliferation of the RAW.267, SH-SY5Y, Caco-2, and RBL-2H3 cancer cell lines, exhibits very low activity against the non-cancerous V79 cell line, and achieves near-complete inhibition of SH-SY5Y cells at a concentration of 50 μM[1].
Stypodiol (up to 500 μM; 48 h) inhibits the viability of human gastric epithelial AGS cells and fibroblasts, with IC50 values of 153 μM and 215 μM, respectively[2].
Stypodiol (24 h) exhibits weak antibacterial activity, with an MIC of 206 μg/mL against E. faecalis[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:RAW.267, SH-SY5Y, Caco-2, RBL-2H3, V79
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Concentration:12.5, 25, 50 µM
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Incubation Time:48 h
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Result:Showed a concentration-dependent inhibitory effect on the proliferation of all tested cancer cell lines, but exhibited less toxicity to the non-cancer cell line V79, demonstrating selectivity.
体内実験
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Swiss albino mice (30 g)[2]
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Dosage:40 mg/kg
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Administration:p.o.; single dose; 50 min pre-treatment prior to 1 h of HCl/EtOH induction
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Result:Reduced the appearance of gastric mucosal lesions.
Decreased the gastric lesion index by 69%.
化学情報
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CAS 番号 71106-25-7
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分子量 428.60
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分子式 C27H40O4
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SMILES
C[C@]12[C@@]3([C@H](CC[C@]1([H])[C@@]4([C@@](C(C)([C@H](CC4)O)C)([H])CC2)C)C)CC5=C(O)C(O)=CC(C)=C5O3
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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
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)