Aporphine alkaloid of sacred and blue lotus. Acts as a dopamine D2 antagonist and weak partial agonist at several serotonin receptors — producing mild sedation, calm, and a subtly dreamy mood-lift.
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CN1CCC2=CC(=C(C3=C2C1CC4=CC=CC=C43)OC)OC The pharmacological targets through which this compound exerts its effects.
Living organisms in which this compound is naturally found.
The most widely consumed psychoactive substance on Earth. Acts primarily as a competitive antagonist of adenosine receptors, indirectly raising dopamine, norepinephrine, and acetylcholine signaling — producing wakefulness, alertness, and mild euphoria.
Excitotoxic glutamate-receptor agonist (NMDA and AMPA) found in Amanita muscaria and A. pantherina. Decarboxylates to the much less excitotoxic muscimol when the mushroom is dried, aged, or passed through a mammalian kidney — which is why dried muscaria (and reindeer-filtered urine) are traditionally preferred over fresh.
Best-characterized of the kavalactones of Piper methysticum. Modulates GABA-A receptors and inhibits voltage-gated sodium and calcium channels — producing a clear-headed, sociable anxiolytic effect quite distinct from alcohol or benzodiazepines.
Principal alkaloid of fermented Sceletium tortuosum. A selective serotonin reuptake inhibitor and PDE4 inhibitor with mild mood-elevating, anxiolytic, and pro-social effects.
