bilobalide
chemical compound
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bilobalide
Summary
bilobalide is a type of chemical entity[1]. bilobalide ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (54 views/month).[2]
Key Facts
- bilobalide's instance of is recorded as type of chemical entity[3].
- bilobalide's physically interacts with is recorded as 5-hydroxytryptamine receptor 3A[4].
- bilobalide's physically interacts with is recorded as Glycine receptor alpha 1[5].
- bilobalide's physically interacts with is recorded as Glycine receptor alpha 2[6].
- bilobalide's physically interacts with is recorded as Glycine receptor beta[7].
- bilobalide's canonical SMILES is recorded as CC(C)(C)C1(CC2C3(C14C(C(=O)OC4OC3=O)O)CC(=O)O2)O[8].
- bilobalide's chemical formula is recorded as C₁₅H₁₈O₈[9].
- bilobalide is a type of 9-Tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.01,11.04,8]tetradecane-2,6,13-trione[10].
- bilobalide is used for medication[11].
- bilobalide's Commons category is recorded as Bilobalide[12].
- bilobalide's found in taxon is recorded as Ginkgo biloba[13].
- bilobalide's isomeric SMILES is recorded as CC(C)(C)[C@@]1(C[C@H]2[C@@]3([C@]14C@HO)CC(=O)O2)OC@HO)CC(=O)O2)O">[14].
- bilobalide's mass is recorded as {'unit': 'Q483261', 'amount': '+326.100168'}[15].
- bilobalide's subject has role is recorded as nootropic[16].
- bilobalide's stereoisomer of is recorded as (-)-Bilobalide[17].
- bilobalide's defined daily dose is recorded as {'unit': 'Q41803', 'amount': '+0.12'}[18].
Why It Matters
bilobalide ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (54 views/month).[2] bilobalide has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[19] bilobalide is known by 14 alternative names across languages and contexts.[20]