Cannabidiol

CAS : 13956-29-1

Ref. 3D-FC19666

Informations sur le produit

• Nom: Cannabidiol
• Synonymes: 2-[(1R,6R)-3-Methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-1,3-benzenediolCBD, (-)-trans-2-p-Mentha-1,8-dien-3-yl-5-pentylresorcinol, 1,3-Benzenediol, 2-(3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl)-5-pentyl-, (1R-trans)-, 1,3-Benzenediol, 2-[(1R,6R)-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-, 2-[(1R,6R)-3-Methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-1,3-benzenediol, 2-[(1R,6R)-3-methyl-6-(prop-1-en-2-yl)cyclohex-2-en-1-yl]-5-pentylbenzene-1,3-diol, 2-[(6R)-3-methyl-6-(prop-1-en-2-yl)cyclohex-2-en-1-yl]-5-pentylbenzene-1,3-diol, CBD, Epidiolex, Epidyolex, Gwp 42003P, Resorcinol, 2-p-mentha-1,8-dien-3-yl-5-pentyl-, (-)-(E)-, Resorcinol, 2-p-mentha-1,8-dien-3-yl-5-pentyl-, trans-(-)-, Δ1(2)-trans-Cannabidiol, Δ¹⁽²⁾-trans-Cannabidiol

Description

Cannabidiol is a non-psychoactive phytocannabinoid with low affinity for the CB1 and CB2 receptor (Ki = 4900 nM and 4200 nM, respectively) (Thomas, 2007). Despite its low affinity, it is able to antagonize cannabinoid CB1 and CB2 receptors at low nanomolar range in murine brain cells and Chinese hamster ovary transfected cells (Thomas, 2007). It has been demonstrated to inhibit immune cell chemotaxis and reducing inflammation processes by acting as an inverse agonist at the CB2 receptor (Lunn, 2006). In rodent in vivo models, cannabidiol encourages neurogenesis and prevents as well as proof of principle reversal of cognitive disease development in AlzheimerÂŽs disease rodent models (Watt and Karl, 2017).

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 314.46 g/mol
• Formule: C₂₁H₃₀O₂
• Degré de pureté: Min. 98 Area-%
• Couleur/Forme: Powder
• InChI: InChI=1S/C21H30O2/c1-5-6-7-8-16-12-19(22)21(20(23)13-16)18-11-15(4)9-10-17(18)14(2)3/h11-13,17-18,22-23H,2,5-10H2,1,3-4H3/t17-,18+/m0/s1
• Code InChI: InChIKey=QHMBSVQNZZTUGM-ZWKOTPCHSA-N
• SMILES: C=C(C)[C@@H]1CCC(C)=C[C@H]1c1c(O)cc(CCCCC)cc1O