Beta-Sitosterol
CAS No. 83-46-5
Beta-Sitosterol( β-Sitosterol | 22,23-Dihydrostigmasterol )
Catalog No. M19156 CAS No. 83-46-5
β-Sitosterol has recently been shown to induce G2/M arrest, endoreduplication, and apoptosis through the Bcl-2 and PI3K/Akt signaling pathways.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | 180 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameBeta-Sitosterol
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NoteResearch use only, not for human use.
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Brief Descriptionβ-Sitosterol has recently been shown to induce G2/M arrest, endoreduplication, and apoptosis through the Bcl-2 and PI3K/Akt signaling pathways.
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Descriptionβ-Sitosterol has recently been shown to induce G2/M arrest, endoreduplication, and apoptosis through the Bcl-2 and PI3K/Akt signaling pathways. β-Sitosterol, a main dietary phytosterol found in plants, may have the potential for prevention and therapy for human cancer. Although the exact mechanism of action of β-sitosterols is unknown, it may be related to cholesterol metabolism or anti-inflammatory effects (via interference with prostaglandin metabolism). β-Sitosterol induces apoptosis and activates key caspases in MDA-MB-231 human breast cancer cells.(In Vitro):Beta-Sitosterol is one of the most abundant dietary phytosterols. Beta-Sitosterol shows anticancer properties against breast cancer, prostate cancer, colon cancer, lung cancer, stomach cancer, ovarian cancer, and leukemia.
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In VitroCell Cytotoxicity Assay Cell Line:MDA-MB-231 Concentration:16 μM Incubation Time:3 days Result:No cytotoxicity at 16 μM Apoptosis Analysis Cell Line:MDA-MB-231 Concentration:16 μM Incubation Time:5 days Result:Increased 33% apoptosis when assayed using 1×104 cells and a 6-fold increase in apoptosis when assayed using a smaller number of cells 5×103.Western Blot Analysis Cell Line:COLO 320 DM Concentration:15, 30, 60, 120 μM Incubation Time:24 h Result:Decreased β-catenin and PCNA expression.
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In VivoAnimal Model:Colon cancer rats model Dosage:10, 20 mg/kg Administration:p.o., suspended in 0.1% CMC (1.0 mL)Result:Reduced the number of aberrant crypt and crypt multiplicity in a dose-dependent manner.Animal Model:Streptozotocin-induced hyperglycemia rats model Dosage:10, 15, 20 mg/kg Administration:p.o.Result:Increased insulin levels and decreased HbA1c levels.Improved pancreatic antioxidant levels and decreased LPO levels.
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Synonymsβ-Sitosterol | 22,23-Dihydrostigmasterol
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PathwayOthers
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TargetOther Targets
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RecptorPPL
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Research AreaMetabolic Disease
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Indication——
Chemical Information
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CAS Number83-46-5
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Formula Weight414.72
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Molecular FormulaC29H50O
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Purity>98% (HPLC)
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SolubilityDMSO : < 1 mg/mL; H2O : < 0.1 mg/mL
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SMILES[C@@H]1(O)CC2=CC[C@@H]3[C@@H]([C@]2(CC1)C)CC[C@]1([C@H]3CC[C@@H]1[C@@H](CC[C@H](C(C)C)CC)C)C
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Chemical Name(24R)-Ethylcholest-5-en-3beta-ol
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Wong HS, et al. PhytOthers Res. 2014 Jul;28(7):999-1006.
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