L-selenocysteine

Summary

L-selenocysteine is a type of chemical entity^[1]. L-selenocysteine ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (106 views/month).^[2]

Key Facts

• L-selenocysteine is credited with the discovery of Thressa Stadtman^[3].
• L-selenocysteine's instance of is recorded as type of chemical entity^[4].
• L-selenocysteine's canonical SMILES is recorded as C(C(C(=O)O)N)[SeH]^[5].
• L-selenocysteine's chemical formula is recorded as C₃H₇NO₂Se^[6].
• L-selenocysteine is a type of (DL)-selenocysteine^[7].
• L-selenocysteine's Commons category is recorded as Selenocysteine^[8].
• L-selenocysteine comprises nitrogen^[9].
• L-selenocysteine comprises carbon^[10].
• L-selenocysteine comprises selenium^[11].
• L-selenocysteine comprises hydrogen^[12].
• L-selenocysteine comprises oxygen^[13].
• L-selenocysteine's found in taxon is recorded as Onion^[14].
• L-selenocysteine's found in taxon is recorded as Allium sativum^[15].
• L-selenocysteine's found in taxon is recorded as Brassica oleracea^[16].
• L-selenocysteine's found in taxon is recorded as Homo sapiens^[17].
• L-selenocysteine's isomeric SMILES is recorded as C(C@@HN)[SeH]^{C@@HN)[SeH]">[18]}.
• L-selenocysteine's mass is recorded as {'unit': 'Q483261', 'amount': '+168.964'}^[19].
• L-selenocysteine's subject has role is recorded as primary metabolite^[20].
• L-selenocysteine's stereoisomer of is recorded as D-selenocysteine^[21].
• L-selenocysteine's tautomer of is recorded as L-selenocysteine zwitterion^[22].

Body

Works and Contributions

L-selenocysteine is credited with the discovery of Thressa Stadtman^[3].

Why It Matters

L-selenocysteine ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (106 views/month).^[2] L-selenocysteine has Wikipedia articles in 24 language editions, a strong signal of global cultural recognition.^[23] L-selenocysteine is known by 12 alternative names across languages and contexts.^[24]