| Identification | Back Directory | [Name]
(3S,5S,10S,13R,14R,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,7,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol | [CAS]
566-97-2 | [Synonyms]
Δ8-Cholesterol
Cholest-8-en-3-ol, (3β,5α)-
5alpha-cholest-8-en-3beta-ol
(3S,5S,10S,13R,14R,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,7,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol | [Molecular Formula]
C27H46O | [MDL Number]
MFCD00201315 | [MOL File]
566-97-2.mol | [Molecular Weight]
386.65 |
| Chemical Properties | Back Directory | [storage temp. ]
-20°C | [solubility ]
DMF: 3 mg/ml; Ethanol: 2 mg/ml | [form ]
A crystalline solid | [color ]
White to off-white | [InChIKey]
QETLKNDKQOXZRP-XTGBIJOFSA-N | [SMILES]
O[C@@H]1C[C@H]2[C@](CC1)(C3=C([C@H]4[C@@]([C@H](CC4)[C@@H](CCCC(C)C)C)(CC3)C)CC2)C |
| Hazard Information | Back Directory | [Uses]
Zymostenol has been used to study its accumulation and its inhibitory actions on Δ8,7-sterol isomerase (EBP). | [Uses]
Zymostenol, is the derivative of Zymosterol (Z701520), which is an sterol intermediate in the biosynthesis of cholesterol (C432501). | [Definition]
ChEBI: A cholestanoid that is 5alpha-cholestane substituted by a beta-hydroxy group at position 3. | [General Description]
Zymostenol acts as a substrate for Δ8,7-sterol isomerase (EBP). It is a demethylation product of 24,25-dihydrolanosterol (24,25-DHL). | [IC 50]
Human Endogenous Metabolite; RORγ: 1 μM (EC50) | [storage]
Store at -20°C |
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