S-adenosyl-L-homocysteine
chemical compound
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S-adenosyl-L-homocysteine
Summary
S-adenosyl-L-homocysteine is a type of chemical entity[1]. S-adenosyl-L-homocysteine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (88 views/month).[2]
Key Facts
- S-adenosyl-L-homocysteine's instance of is recorded as type of chemical entity[3].
- S-adenosyl-L-homocysteine's canonical SMILES is recorded as C1=NC2=C(C(=N1)N)N=CN2C3C(C(C(O3)CSCCC(C(=O)O)N)O)O[4].
- S-adenosyl-L-homocysteine's chemical formula is recorded as C₁₄H₂₀N₆O₅S[5].
- S-adenosyl-L-homocysteine is a type of alkaloid[6].
- S-adenosyl-L-homocysteine is part of S-adenosylhomocysteine catabolic process[7].
- S-adenosyl-L-homocysteine is part of S-adenosylhomocysteine metabolic process[8].
- S-adenosyl-L-homocysteine is part of S-adenosylmethionine cycle[9].
- S-adenosyl-L-homocysteine's Commons category is recorded as S-Adenosyl-L-homocysteine[10].
- S-adenosyl-L-homocysteine comprises nitrogen[11].
- S-adenosyl-L-homocysteine comprises carbon[12].
- S-adenosyl-L-homocysteine's found in taxon is recorded as Homo sapiens[13].
- S-adenosyl-L-homocysteine's found in taxon is recorded as Escherichia coli[14].
- S-adenosyl-L-homocysteine's found in taxon is recorded as Caenorhabditis elegans[15].
- S-adenosyl-L-homocysteine's isomeric SMILES is recorded as C1=NC2=C(C(=N1)N)N=CN2[C@H]3C@@HOC@@HO">[16].
- S-adenosyl-L-homocysteine's mass is recorded as {'unit': 'Q483261', 'amount': '+384.122'}[17].
- S-adenosyl-L-homocysteine's subject has role is recorded as primary metabolite[18].
- S-adenosyl-L-homocysteine's stereoisomer of is recorded as (2S)-2-amino-4-[[(2R,3R,4S,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methylsulfanyl]butanoic acid[19].
- S-adenosyl-L-homocysteine's stereoisomer of is recorded as S-adenosyl-L-homocysteine zwitterion[20].
- S-adenosyl-L-homocysteine's stereoisomer of is recorded as (2R)-2-Amino-4-({[(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl}sulfanyl)butanoic acid (non-preferred name)[21].
- S-adenosyl-L-homocysteine's tautomer of is recorded as S-adenosyl-L-homocysteine zwitterion[22].
Why It Matters
S-adenosyl-L-homocysteine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (88 views/month).[2] S-adenosyl-L-homocysteine has Wikipedia articles in 13 language editions, a strong signal of global cultural recognition.[23] S-adenosyl-L-homocysteine is known by 15 alternative names across languages and contexts.[24]