Etiocholanolone

CAT:
804-HY-113320-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Etiocholanolone - image 1

Etiocholanolone

  • Description:

    Etiocholanolone (5β-Androsterone) is the excreted metabolite of testosterone and has anticonvulsant activity[1]. Etiocholanolone is a less potent neurosteroid positive allosteric modulator (PAM) of the GABAA receptor than its enantiomer form[2].
  • Product Name Alternative:

    5β-Androsterone
  • UNSPSC:

    12352211
  • Hazard Statement:

    H302, H351, H361, H410
  • Target:

    Endogenous Metabolite; GABA Receptor
  • Type:

    Natural Products
  • Related Pathways:

    Membrane Transporter/Ion Channel; Metabolic Enzyme/Protease; Neuronal Signaling
  • Applications:

    Neuroscience-Neuromodulation
  • Field of Research:

    Neurological Disease
  • Assay Protocol:

    https://www.medchemexpress.com/etiocholanolone.html
  • Purity:

    99.49
  • Solubility:

    DMSO : 50 mg/mL (ultrasonic; warming; heat to 60°C)
  • Smiles:

    C[C@@]1(CC2)[C@](CC3)([H])[C@](CC[C@]1([H])C[C@@H]2O)([H])[C@@](CCC4=O)([H])[C@]34C
  • Molecular Formula:

    C19H30O2
  • Molecular Weight:

    290.44
  • Precautions:

    H302, H351, H361, H410
  • References & Citations:

    [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.|[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.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

    -20°C, 3 years; 4°C, 2 years (Powder)
  • Scientific Category:

    Natural Products
  • Clinical Information:

    No Development Reported
  • Isoform:

    Human Endogenous Metabolite
  • CAS Number:

    53-42-9