CHEBI:16633 - L-selenocysteine

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ChEBI Name L-selenocysteine
ChEBI ID CHEBI:16633
ChEBI ASCII Name L-selenocysteine
Definition The L-enantiomer of selenocysteine.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:21385, CHEBI:49562, CHEBI:6298, CHEBI:13165
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Formula C3H7NO2Se
Net Charge 0
Average Mass 168.065
Monoisotopic Mass 168.96420
InChI InChI=1S/C3H7NO2Se/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6)/t2-/m0/s1
InChIKey ZKZBPNGNEQAJSX-REOHCLBHSA-N
SMILES C([C@@H](C(O)=O)N)[SeH]
Metabolite of Species Details
Homo sapiens (NCBI:txid9606) See: PubMed
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via selenocysteine )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing L-selenocysteine (CHEBI:16633) has role human metabolite (CHEBI:77746)
L-selenocysteine (CHEBI:16633) is a L-α-amino acid (CHEBI:15705)
L-selenocysteine (CHEBI:16633) is a L-alanine derivative (CHEBI:83943)
L-selenocysteine (CHEBI:16633) is a proteinogenic amino acid (CHEBI:83813)
L-selenocysteine (CHEBI:16633) is a selenocysteine (CHEBI:9093)
L-selenocysteine (CHEBI:16633) is conjugate acid of L-selenocysteinate(1−) (CHEBI:32742)
L-selenocysteine (CHEBI:16633) is conjugate base of L-selenocysteinium (CHEBI:32744)
L-selenocysteine (CHEBI:16633) is enantiomer of D-selenocysteine (CHEBI:30001)
L-selenocysteine (CHEBI:16633) is tautomer of L-selenocysteine zwitterion (CHEBI:57843)
Incoming L-selenocysteine derivative (CHEBI:84209) has functional parent L-selenocysteine (CHEBI:16633)
L-selenocysteinium (CHEBI:32744) is conjugate acid of L-selenocysteine (CHEBI:16633)
L-selenocysteinate(1−) (CHEBI:32742) is conjugate base of L-selenocysteine (CHEBI:16633)
D-selenocysteine (CHEBI:30001) is enantiomer of L-selenocysteine (CHEBI:16633)
L-selenocysteine residue (CHEBI:30000) is substituent group from L-selenocysteine (CHEBI:16633)
L-selenocysteino group (CHEBI:32746) is substituent group from L-selenocysteine (CHEBI:16633)
L-selenocysteinyl group (CHEBI:32745) is substituent group from L-selenocysteine (CHEBI:16633)
L-selenocysteine zwitterion (CHEBI:57843) is tautomer of L-selenocysteine (CHEBI:16633)
IUPAC Name
(2R)-2-amino-3-selanylpropanoic acid
Synonyms Sources
3-selenyl-L-alanine ChemIDplus
L-Selenocystein ChEBI
L-Selenocysteine KEGG COMPOUND
L-Selenozystein ChEBI
SELENOCYSTEINE PDBeChem
Selenocysteine ChemIDplus
Manual Xrefs Databases
C05688 KEGG COMPOUND
ECMDB03288 ECMDB
HMDB0003288 HMDB
L-SELENOCYSTEINE MetaCyc
SEC PDBeChem
Selenocysteine Wikipedia
View more database links
Registry Numbers Types Sources
10236-58-5 CAS Registry Number ChemIDplus
2498378 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
11733012 PubMed citation Europe PMC
18429173 PubMed citation Europe PMC
Last Modified
21 November 2019