lysergic acid diethylamide
chemical compound
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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 (9,283 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 1938[20].
- lysergic acid diethylamide's time of discovery or invention is recorded as 1948[21].
- lysergic acid diethylamide's route of administration is recorded as sublingual administration[22].
- lysergic acid diethylamide's found in taxon is recorded as Claviceps[23].
- lysergic acid diethylamide's topic's main category is recorded as Category:Lysergic acid diethylamide[24].
- lysergic acid diethylamide's described by source is recorded as Opium Law[25].
- 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[26].
- lysergic acid diethylamide's mass is recorded as {'amount': '+323.199762'}[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 (9,283 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 64 alternative names across languages and contexts.[29]