Etiocholanolone (Standard)
Etiocholanolone (Standard) (5β-Androsterone (Standard)) is the analytical standard of Etiocholanolone (HY-113320). This product is intended for research and analytical applications. Etiocholanolone (5β-Androsterone) is the excreted metabolite of testosterone and has anticonvulsant activity. Etiocholanolone is a less potent neurosteroid positive allosteric modulator (PAM) of the GABAA receptor than its enantiomer form.
For research use only. We do not sell to patients.
- Purity : 98%
- CAS No.: 53-42-9
- Formula: C19H30O2
- Molecular Weight:290.44
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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-113320
EtiocholanoloneMetabolite Of Testosterone -
HY-14650
DHEASteroid Hormone -
HY-111614
Melengestrol acetateContraceptive Agent -
HY-B0521
AltrenogestProgesterone Receptor Agonist -
HY-14650R
DHEA (Standard)Analytical Standard of DHEA -
HY-111614R
Melengestrol acetate (Standard) -
HY-B0521R
Altrenogest (Standard)Progesterone Receptor Agonist
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. 53-42-9
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Molecular Weight 290.44
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Formula C19H30O2
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SMILES
C[C@@]1(CC2)[C@](CC3)([H])[C@](CC[C@]1([H])C[C@@H]2O)([H])[C@@](CCC4=O)([H])[C@]34C
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Synonyms
5β-Androsterone (Standard)
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Structure Classification
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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]. Ping Li,et al. Natural and Enantiomeric Etiocholanolone Interact With Distinct Sites on the Rat alpha1beta2gamma2L GABAA Receptor. Mol Pharmacol. 2007 Jun;71(6):1582-90. [Content Brief]
[2]. Dorota Zolkowska, et al. Anticonvulsant Potencies of the Enantiomers of the Neurosteroids Androsterone and Etiocholanolone Exceed Those of the Natural Forms. Psychopharmacology (Berl). 2014 Sep;231(17):3325-32. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Etiocholanolone (Standard) Related Classifications
HY-113320R Related Classifications
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