OlivetolOlivetol - High-quality laboratory reagent available from Gentaur. Catalog: 804-HY-W008364-01.804-HY-W008364-01804-HY-W008364-01Business & Industrial > Science & LaboratoryOlivetol
Gentaur
EUR12027-02-22

Olivetol

CAT:
804-HY-W008364-01
Size:
500 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Olivetol - image 1

Olivetol

  • Description:

    Olivetol is a naturally phenol found in lichens and produced by certain insects, acting as a competitive inhibitor of the cannabinoid receptors CB1 and CB2[3]. Olivetol also inhibits CYP2C19 and CYP2D6 activity, with IC50s of 15.3 μM, 7.21 μM and Kis of 2.71 μM, 2.87 μM, respectively[1][2].
  • UNSPSC:

    12352005
  • Hazard Statement:

    H302, H315, H318, H400
  • Target:

    Cannabinoid Receptor; Cytochrome P450
  • Type:

    Natural Products
  • Related Pathways:

    GPCR/G Protein; Metabolic Enzyme/Protease; Neuronal Signaling
  • Applications:

    Neuroscience-Neuromodulation
  • Field of Research:

    Neurological Disease
  • Assay Protocol:

    https://www.medchemexpress.com/Olivetol.html
  • Concentration:

    10mM
  • Purity:

    99.86
  • Solubility:

    DMSO : 100 mg/mL (ultrasonic)
  • Smiles:

    OC1=CC(CCCCC)=CC(O)=C1
  • Molecular Formula:

    C11H16O2
  • Molecular Weight:

    180.25
  • Precautions:

    H302, H315, H318, H400
  • References & Citations:

    [1]Jiang R, et al. Cannabidiol is a potent inhibitor of the catalytic activity of cytochrome P450 2C19. Drug Metab Pharmacokinet. 2013;28 (4) :332-8.|[2]Yamaori S, et al. Cannabidiol, a major phytocannabinoid, as a potent atypical inhibitor for CYP2D6. Drug Metab Dispos. 2011 Nov;39 (11) :2049-56.|[3]James J. Carberry , et al. Composition of Olivetol and Method of Use to Reduce or Inhibit the Effects of Tetrahydrocannabinol in the Human Body. US20170143644A1
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

    4°C (Powder, stored under nitrogen)
  • Scientific Category:

    Natural Products
  • Clinical Information:

    No Development Reported
  • Isoform:

    CYP2
  • CAS Number:

    [500-66-3]