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.
Nos produits utilisent uniquement pour la recherche. Nous ne vendons pas aux patients.
- Pureté : 98%
- CAS No.: 53-42-9
- Formule: C19H30O2
- Masse moléculaire:290.44
-
Stockage:
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]
-
Product Information
-
Chemical Information
- Pureté et documentation
-
Help & FAQs
-
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
-
CAS No. 53-42-9
-
Masse moléculaire 290.44
-
Formule C19H30O2
-
SMILES
C[C@@]1(CC2)[C@](CC3)([H])[C@](CC[C@]1([H])C[C@@H]2O)([H])[C@@](CCC4=O)([H])[C@]34C
-
Synonyms
5β-Androsterone (Standard)
-
Structure Classification
-
Initial Source
-
Livraison
Room temperature in continental US; may vary elsewhere.
-
Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
[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
Powered by Bioz