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Zymostenol
Catalog No. T35321Cas No. 566-97-2
Alias Δ8-Cholesterol, delta(8)-Cholestenol, 5a-Cholest-8-en-3b-ol
Zymostenol (5a-Cholest-8-en-3b-ol) is a RORγ agonist with an EC50 of 1 μM and serves as a late-stage precursor in cholesterol biosynthesis.
Zymostenol
Catalog No. T35321Alias Δ8-Cholesterol, delta(8)-Cholestenol, 5a-Cholest-8-en-3b-olCas No. 566-97-2
Zymostenol (5a-Cholest-8-en-3b-ol) is a RORγ agonist with an EC50 of 1 μM and serves as a late-stage precursor in cholesterol biosynthesis.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 5 mg | $263 | 35 days | |
| 10 mg | $468 | 35 days | |
| 25 mg | $987 | 35 days | |
| 50 mg | $1,930 | 35 days |
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Product Introduction
Bioactivity
Chemical Properties
| Description | Zymostenol (5a-Cholest-8-en-3b-ol) is a RORγ agonist with an EC50 of 1 μM and serves as a late-stage precursor in cholesterol biosynthesis. |
| Targets&IC50 | RORγ:1 μM(EC50) |
| In vitro | Zymostenol (12-104 μM) promotes the formation of myelin basic protein-positive (MBP+) oligodendrocytes in mouse ectodermal stem cell-derived oligodendrocyte progenitors.[2] Zymostenol (20 μM, 3 days) arrests the MCF-7 cell cycle in the G0-G1 phase.[3] |
| Alias | Δ8-Cholesterol, delta(8)-Cholestenol, 5a-Cholest-8-en-3b-ol |
| Molecular Weight | 386.65 |
| Formula | C27H46O |
| Cas No. | 566-97-2 |
Storage & Solubility Information
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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