lysergic acid diethylamide

Summary

lysergic acid diethylamide is a type of chemical entity^[1]. It ranks in the top 0.1% of type_of_chemical_entity entities by monthly Wikipedia readership (18,546 views/month, #13 of 12,596).^[2]

Key Facts

• lysergic acid diethylamide is credited with the discovery of Albert Hofmann^[3].
• lysergic acid diethylamide's instance of is recorded as type of chemical entity^[4].
• lysergic acid diethylamide's physically interacts with is recorded as 5-hydroxytryptamine receptor 1A^[5].
• lysergic acid diethylamide's physically interacts with is recorded as 5-hydroxytryptamine receptor 2A^[6].
• lysergic acid diethylamide's physically interacts with is recorded as 5-hydroxytryptamine receptor 2B^[7].
• lysergic acid diethylamide's physically interacts with is recorded as 5-hydroxytryptamine receptor 2C^[8].
• lysergic acid diethylamide's physically interacts with is recorded as 5-hydroxytryptamine receptor 6^[9].
• lysergic acid diethylamide's canonical SMILES is recorded as CCN(CC)C(=O)C1CN(C2CC3=CNC4=CC=CC(=C34)C2=C1)C^[10].
• lysergic acid diethylamide's chemical formula is recorded as C₂₀H₂₅N₃O^[11].
• lysergic acid diethylamide is a type of tryptamines^[12].
• lysergic acid diethylamide is a type of phenethylamine^[13].
• lysergic acid diethylamide is used for drug^[14].
• lysergic acid diethylamide is used for medication^[15].
• lysergic acid diethylamide's Commons category is recorded as Lysergic acid diethylamide^[16].
• lysergic acid diethylamide comprises nitrogen^[17].
• lysergic acid diethylamide comprises oxygen^[18].
• lysergic acid diethylamide comprises carbon^[19].
• lysergic acid diethylamide's time of discovery or invention is recorded as 1948^[20].
• lysergic acid diethylamide's route of administration is recorded as sublingual administration^[21].
• lysergic acid diethylamide's found in taxon is recorded as Claviceps^[22].
• lysergic acid diethylamide's topic's main category is recorded as Category:Lysergic acid diethylamide^[23].
• lysergic acid diethylamide's described by source is recorded as Opium Law^[24].
• lysergic acid diethylamide's isomeric SMILES is recorded as CCN(CC)C(=O)[C@H]1CN([C@@H]2CC3=CNC4=CC=CC(=C34)C2=C1)C^[25].
• lysergic acid diethylamide's mass is recorded as {'unit': 'Q483261', 'amount': '+323.199762'}^[26].
• lysergic acid diethylamide's World Health Organisation international non-proprietary name is recorded as {'lang': 'en', 'text': 'lysergide'}^[27].

Body

Works and Contributions

lysergic acid diethylamide is credited with the discovery of Albert Hofmann^[3].

Why It Matters

lysergic acid diethylamide ranks in the top 0.1% of type_of_chemical_entity entities by monthly Wikipedia readership (18,546 views/month, #13 of 12,596).^[2] It has Wikipedia articles in 30 language editions, a strong signal of global cultural recognition.^[28] It is known by 48 alternative names across languages and contexts.^[29]