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.
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- CAS No.: 71106-25-7
- Formule: C27H40O4
- Masse moléculaire:428.60
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Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
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Activité biologique
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Chemical Information
- Pureté et documentation
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Activité biologique
Description
Cellular Effect
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| AGS | IC50 |
153 μM
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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.
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25830679 |
| Fibroblast | IC50 |
215 μM
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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.
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25830679 |
In Vitro
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.
In Vivo
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%.
Chemical Information
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CAS No. 71106-25-7
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Masse moléculaire 428.60
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Formule 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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Livraison
Room temperature in continental US; may vary elsewhere.
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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)
Stypodiol Related Classifications
HY-N21841 Related Classifications
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