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 168.05000
Monoisotopic Mass 168.964
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 N[C@@H](C[SeH])C(O)=O
Metabolite of Species Details
Homo sapiens (NCBI:9606) See: PubMed
Roles Classification
Chemical Role(s): 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 )
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via L-alpha-amino acid )
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
Database Links Databases
C05688 KEGG COMPOUND
CSE PDBeChem
ECMDB03288 ECMDB
HMDB03288 HMDB
L-SELENOCYSTEINE MetaCyc
Selenocysteine Wikipedia
View more database links
Registry Numbers Types Sources
10236-58-5 CAS Registry Number ChemIDplus
2498378 Beilstein Registry Number Beilstein
2498378 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
11733012 PubMed citation Europe PMC
18429173 PubMed citation Europe PMC
Last Modified
02 February 2015