lorcaserin
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lorcaserin
Summary
lorcaserin is a type of chemical entity[1]. lorcaserin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (152 views/month).[2]
Key Facts
- lorcaserin's instance of is recorded as type of chemical entity[3].
- lorcaserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 2A[4].
- lorcaserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 2B[5].
- lorcaserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 2C[6].
- lorcaserin's canonical SMILES is recorded as CC1CNCCC2=C1C=C(C=C2)Cl[7].
- lorcaserin's chemical formula is recorded as C₁₁H₁₄ClN[8].
- lorcaserin is a type of Lorcaserin A[9].
- lorcaserin is used for medication[10].
- lorcaserin's Commons category is recorded as Lorcaserin[11].
- lorcaserin's isomeric SMILES is recorded as C[C@H]1CNCCC2=C1C=C(C=C2)Cl[12].
- lorcaserin's mass is recorded as {'unit': 'Q483261', 'amount': '+195.081477'}[13].
- lorcaserin's World Health Organisation international non-proprietary name is recorded as {'lang': 'en', 'text': 'lorcaserin'}[14].
- lorcaserin's stereoisomer of is recorded as (1S)-8-Chloro-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine[15].
- lorcaserin's pregnancy category is recorded as US pregnancy category X[16].
- lorcaserin's active ingredient in is recorded as Belviq[17].
- lorcaserin's LiverTox likelihood score is recorded as LiverTox toxicity likelihood category E[18].
Why It Matters
lorcaserin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (152 views/month).[2] lorcaserin has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[19] lorcaserin is known by 6 alternative names across languages and contexts.[20]