CHEBI:27812 - Se-methyl-L-selenocysteine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name Se-methyl-L-selenocysteine
ChEBI ID CHEBI:27812
ChEBI ASCII Name Se-methyl-L-selenocysteine
Definition An L-α-amino acid compound having methylselanylmethyl as the side-chain.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:9067, CHEBI:22076
Supplier Information
Download Molfile XML SDF
Formula C4H9NO2Se
Net Charge 0
Average Mass 182.08000
Monoisotopic Mass 182.97985
InChI InChI=1S/C4H9NO2Se/c1-8-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m0/s1
InChIKey XDSSPSLGNGIIHP-VKHMYHEASA-N
SMILES C[Se]C[C@H](N)C(O)=O
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 Se-methylselenocysteine )
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via L-alpha-amino acid )
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
(via Se-methylselenocysteine )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing Se-methyl-L-selenocysteine (CHEBI:27812) has role antineoplastic agent (CHEBI:35610)
Se-methyl-L-selenocysteine (CHEBI:27812) is a Se-methylselenocysteine (CHEBI:9068)
Se-methyl-L-selenocysteine (CHEBI:27812) is a L-selenocysteine derivative (CHEBI:84209)
Se-methyl-L-selenocysteine (CHEBI:27812) is a non-proteinogenic L-α-amino acid (CHEBI:83822)
Se-methyl-L-selenocysteine (CHEBI:27812) is conjugate acid of Se-methyl-L-selenocysteinate (CHEBI:53126)
Se-methyl-L-selenocysteine (CHEBI:27812) is conjugate base of Se-methyl-L-selenocysteinium (CHEBI:53130)
Se-methyl-L-selenocysteine (CHEBI:27812) is enantiomer of Se-methyl-D-selenocysteine (CHEBI:53125)
Se-methyl-L-selenocysteine (CHEBI:27812) is tautomer of Se-methyl-L-selenocysteine zwitterion (CHEBI:58531)
Incoming Se-methyl-L-selenocysteinium (CHEBI:53130) is conjugate acid of Se-methyl-L-selenocysteine (CHEBI:27812)
Se-methyl-L-selenocysteinate (CHEBI:53126) is conjugate base of Se-methyl-L-selenocysteine (CHEBI:27812)
Se-methyl-D-selenocysteine (CHEBI:53125) is enantiomer of Se-methyl-L-selenocysteine (CHEBI:27812)
Se-methyl-L-selenocysteine residue (CHEBI:53134) is substituent group from Se-methyl-L-selenocysteine (CHEBI:27812)
Se-methyl-L-selenocysteino group (CHEBI:53140) is substituent group from Se-methyl-L-selenocysteine (CHEBI:27812)
Se-methyl-L-selenocysteinyl group (CHEBI:53137) is substituent group from Se-methyl-L-selenocysteine (CHEBI:27812)
Se-methyl-L-selenocysteine zwitterion (CHEBI:58531) is tautomer of Se-methyl-L-selenocysteine (CHEBI:27812)
IUPAC Name
(2R)-2-amino-3-methylselanylpropanoic acid
Synonyms Sources
L-methylselenocysteine ChEBI
methyl-L-selenocysteine ChEBI
Methylselenocysteine ChemIDplus
Se-Methyl-L-selenocysteine KEGG COMPOUND
Se-methyl-seleno-L-cysteine ChemIDplus
Se-Methyl-selenocysteine ChemIDplus
Se-methylselenocysteine ChemIDplus
Selenium methyl cysteine ChemIDplus
Selenium-methylselenocystine ChemIDplus
Selenohomocysteine ChemIDplus
Selenomethylselenocysteine ChemIDplus
Manual Xref Database
C05689 KEGG COMPOUND
View more database links
Registry Numbers Types Sources
2574-71-2 CAS Registry Number KEGG COMPOUND
2574-71-2 CAS Registry Number ChemIDplus
26046-90-2 CAS Registry Number ChemIDplus
2636762 Beilstein Registry Number Beilstein
Last Modified
26 March 2015