| CB1R | Cannabinoid receptor type 1 |
| GPCR | G protein-coupled receptor |
| ECL2 | Extracellular loop 2 |
| ECS | Endocannabinoid system |
| AEA | Anandamide |
| 2-AG | 2-Arachidonoylglycerol |
| CB2R | Cannabinoid receptor type 2 |
| FAAH | Fatty acid amide hydrolase |
| MGL | Monoacylglycerol lipase |
| NMR | Nuclear magnetic resonance |
| EPR | Electron paramagnetic resonance |
| MS | Mass spectrometry |
| FRET | Fluorescence resonance energy transfer |
| X-ray | X-ray crystallography |
| IUPHAR | The International Union of Basic and Clinical Pharmacology |
| 7TMRs | Seven-Transmembrane Receptors |
| NALs | Neutral allosteric ligands |
| CNR1 | Cannabinoid receptor 1 gene |
| kDa | Kilo Dalton |
| TMH | Transmembrane-helix |
| ICL | Intracellular loop |
| ∆-9-THC | Delta 9 tetrahydrocannabinol |
| CP 55,940 | [2-((1R,2R,5R)-5-hydroxy-2-(3-hydroxypropyl)cyclohexyl)-5-(2-methyloctan-2-yl)phenol] |
| HU-210 | [(6aR,10aR)-9-(hydroxymethyl)-6,6-dimethyl-3-(2-methyloctan-2-yl)-6a,7,10,10a-tetra-hydro-6H-benzo[c]chromen-1-ol]- |
| WIN 55212-2 | [(R)-(5-methyl-3-(morpholinomethyl)-2,3-dihydro-[1,4]oxazino[2,3,4-hi]indol-6-yl)-(naphthalen-1-yl)methanone] |
| JWH-018 | [Naphthalen-1-yl-(1-pentylindol-3-yl)methanone] |
| SR-141716A (rimonabant) | [5-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-N-(1-piperidinyl)-1H-pyrazole-3-carboxamide] |
| AM251 | [1-(2,4-Dichlorophenyl)-5-(4-iodophenyl)-4-methyl-N-(1-piperidinyl)-1-pyrazole-3-carboxamide] |
| AIDS | Acquired immunodeficiency syndrome |
| FDA | Food and Drug Administration |
| cAMP | Cyclic adenosine monophosphate |
| PKA | Protein kinase A |
| PKB | Protein kinase B |
| MAPKs | Mitogen-activated protein kinases |
| ERK | Extracellular signal-regulated protein kinase |
| JNK | C-JUN N-terminal kinase |
| PI3K | Phosphoinositide 3-kinases |
| AP-3 | Adaptor protein 3 |
| GASP | GPCR-associated sorting proteins |
| FAN | Factor associated with neutral sphingomyelinase activation |
| CRIP1a | Cannabinoid receptor-interacting protein 1a |
| VGCC | Voltage-gated calcium channel |
| GIRK | G-protein-coupled inwardly rectifying potassium channels |
| A2A | Adenosine receptor dopamine D2 |
| D2 | Dopamine receptor |
| CCR2 | Chemokine (C-C motif) receptor type 2 |
| CCR9 | Chemokine (C-C motif) receptor type 9 |
| β-2AR | Beta-2 adrenergic receptor |
| mtCB1 | Mitochondrial cannabinoid receptor |
| sAC | Soluble adenylyl cyclase |
| MECA | Melanocortin, endothelial differentiation, cannabinoid, adenosine cluster |
| AA2AR | adenosine A2A receptor |
| CWxP | Cys-Trp-Xaa-Pro motif |
| EC | Extracellular |
| Cys | Cysteine |
| MPR | Membrane proximal region |
| Org | Organon |
| PAM | Positive allosteric modulator |
| NAM | Negative allosteric modulator |
| SAR | Structure–activity relationship |
| MDMB-Fubinaca | Indazole-based synthetic cannabinoid |
| LXA4 | Lipoxin 4 |
| CBD | Cannabidiol |
| DAT | Dopamine active transporter |
| RTI-371 | 3β-(4-Methylphenyl)-2β-[3-(4-chlorophenyl)isoxazol-5-yl]tropane |
| 7TMR | Seven-Transmembrane Receptors |