methylselenocysteine
chemical compound
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methylselenocysteine
Summary
methylselenocysteine is a type of chemical entity[1]. methylselenocysteine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (19 views/month).[2]
Key Facts
- methylselenocysteine's instance of is recorded as type of chemical entity[3].
- methylselenocysteine's canonical SMILES is recorded as C[Se]CC(C(=O)O)N[4].
- methylselenocysteine's chemical formula is recorded as C₄H₉NO₂Se[5].
- methylselenocysteine is a type of Se-methylselenocysteine[6].
- methylselenocysteine's Commons category is recorded as Methylselenocysteine[7].
- methylselenocysteine comprises carbon[8].
- methylselenocysteine comprises selenium[9].
- methylselenocysteine comprises nitrogen[10].
- methylselenocysteine comprises oxygen[11].
- methylselenocysteine comprises hydrogen[12].
- methylselenocysteine's found in taxon is recorded as Astragalus bisulcatus[13].
- methylselenocysteine's isomeric SMILES is recorded as C[Se]CC@@HNC@@HN">[14].
- methylselenocysteine's mass is recorded as {'unit': 'Q483261', 'amount': '+182.97985'}[15].
- methylselenocysteine's subject has role is recorded as anticarcinogens[16].
- methylselenocysteine's subject has role is recorded as primary metabolite[17].
- methylselenocysteine's stereoisomer of is recorded as Se-methyl-L-selenocysteine zwitterion[18].
- methylselenocysteine's stereoisomer of is recorded as Se-methyl-D-selenocysteine[19].
- methylselenocysteine's tautomer of is recorded as Se-methyl-L-selenocysteine zwitterion[20].
Why It Matters
methylselenocysteine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (19 views/month).[2] methylselenocysteine has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[21] methylselenocysteine is known by 11 alternative names across languages and contexts.[22]