Cannabidiol
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4 sources
🧬 Receptor activity
| Target | Action | Affinity | Source | |
|---|---|---|---|---|
| G-protein coupled receptor 55 (GPR55) | Antagonist | 6.35 EC50 | DRUGCENTRAL | TargetG-protein coupled receptor 55 (GPR55) ActionAntagonist Affinity6.35 EC50 SourceDRUGCENTRAL |
| N-arachidonyl glycine receptor (GPR18) | Agonist | 4.29 EC50 | DRUGCENTRAL | TargetN-arachidonyl glycine receptor (GPR18) ActionAgonist Affinity4.29 EC50 SourceDRUGCENTRAL |
| Transient receptor potential cation channel subfamily V member 1 (TRPV1) | Inhibitor | — | DRUGCENTRAL | TargetTransient receptor potential cation channel subfamily V member 1 (TRPV1) ActionInhibitor Affinity— SourceDRUGCENTRAL |
| Transient receptor potential cation channel subfamily V member 2 (Trpv2) | Activator | 5.43 EC50 | DRUGCENTRAL | TargetTransient receptor potential cation channel subfamily V member 2 (Trpv2) ActionActivator Affinity5.43 EC50 SourceDRUGCENTRAL |
| Cannabinoid receptor 1 (CNR1) | — | 5.62 Ki | DRUGCENTRAL | TargetCannabinoid receptor 1 (CNR1) Action— Affinity5.62 Ki SourceDRUGCENTRAL |
| Cannabinoid receptor 2 (CNR2) | — | 5.54 Ki | DRUGCENTRAL | TargetCannabinoid receptor 2 (CNR2) Action— Affinity5.54 Ki SourceDRUGCENTRAL |
| Fatty-acid amide hydrolase 1 (Faah) | — | 4.27 IC50 | DRUGCENTRAL | TargetFatty-acid amide hydrolase 1 (Faah) Action— Affinity4.27 IC50 SourceDRUGCENTRAL |
External links
PubChem 644019 ↗CAS 13956-29-1 ↗KEGG C07578 ↗ChEBI CHEBI:69478 ↗ChEMBL CHEMBL190461 ↗KEGG D10915 ↗DrugBank DB09061 ↗NIH ↗ChemSpider ↗ChEBI/ChEMBL ↗ChEBI/ChEMBL ↗Guide to Pharmacology ↗NIH ↗NIH ↗NIH ↗NIH ↗DrugBank ↗ChEBI/ChEMBL ↗NIH ↗NIH ↗NIH ↗NIH ↗NIH ↗NIH ↗NIH ↗NIH ↗CAS 145514-04-1 ↗CAS 3556-78-3 ↗PsychonautWiki ↗Erowid ↗Experience reports (PiHKAL) ↗Experience reports (TiHKAL) ↗
Source: DrugCentral — Cannabidiol ↗
Fact-sheets from PsychonautWiki. Harm-reduction reference only — not medical advice.