Zymostenol (Standard)
Zymostenol (Standard) (5a-Cholest-8-en-3b-ol (Standard)) is the analytical standard of Zymostenol (HY-113345). This product is intended for research and analytical applications. Zymostenol (5a-Cholest-8-en-3b-ol) is a late-stage precursor in the biosynthesis of cholesterol. Zymostenol is a RORγ agonist (EC50: 1 μM).
For research use only. We do not sell to patients.
- CAS No.: 566-97-2
- Formula: C27H46O
- Molecular Weight:386.65
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Product Information
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Chemical Information
- Purity & Documentation
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Help & FAQs
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HY-113345
ZymostenolRORγ Agonist -
HY-W042191
OxychlororaphineAntifungal Agent -
HY-14422
SR1078RORα/RORγ Agonist -
HY-13421
SR1001RORα/γt Inverse Agonist -
HY-101454
SR0987RORγt Agonist -
HY-104037
CintirorgonRORγ Agonist -
HY-120210
XY018ROR-γ Antagonist -
HY-138115
7ß,27-DihydroxycholesterolRORγt Activator -
HY-19775
GNE-6468RORγ (RORc) Inverse Agonist -
HY-N10546A
Ganglioside GM1 (bovine) ammoniumGlycosphingolipid -
HY-120785
SR1555RORγ Inverse Agonist -
HY-137307
Cholest-5-ene-3ß,22(S)-diolOxysterol
Product Information
Information
Application
The compound is the grade of analytical standard, which is the reference standard supplied assay. It is commonly used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS.
Chemical Information
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CAS No. 566-97-2
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Molecular Weight 386.65
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Formula C27H46O
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SMILES
CC(C)CCC[C@@H](C)[C@H]1CC[C@@]2([H])C(CC[C@@]3([H])C[C@@H](O)CC[C@]43C)=C4CC[C@]12C
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Synonyms
5a-Cholest-8-en-3b-ol (Standard)
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Initial Source
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
[1]. Hu X, et al. Sterol metabolism controls T(H)17 differentiation by generating endogenous RORγ agonists. Nat Chem Biol. 2015 Feb;11(2):141-7. [Content Brief]
[2]. Hubler Z, et al. Accumulation of 8,9-unsaturated sterols drives oligodendrocyte formation and remyelination. Nature. 2018 Aug;560(7718):372-376. [Content Brief]
[3]. Payré B, et al. Microsomal antiestrogen-binding site ligands induce growth control and differentiation of human breast cancer cells through the modulation of cholesterol metabolism. Mol Cancer Ther. 2008 Dec;7(12):3707-18. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Zymostenol (Standard) Related Classifications
HY-113345R Related Classifications
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