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CHEBI:27812 - Se-methyl-L-selenocysteine

ChEBI IDCHEBI:27812
ChEBI NameSe-methyl-L-selenocysteine
Stars
ASCII NameSe-methyl-L-selenocysteine
DefinitionAn L-α-amino acid compound having methylselanylmethyl as the side-chain.
Secondary ChEBI IDsCHEBI:9067, CHEBI:22076
Last Modified26 March 2015
DownloadsMolfile
FormulaC4H9NO2Se
Net Charge0
Average Mass182.081
Monoisotopic Mass182.97985
SMILESC[Se]C[C@H](N)C(=O)O
InChIInChI=1S/C4H9NO2Se/c1-8-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m0/s1
InChIKeyXDSSPSLGNGIIHP-VKHMYHEASA-N
Roles Classification
Chemical Roles:
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Biological Role:
human metabolite  Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
Applications:
antineoplastic agent  A substance that inhibits or prevents the proliferation of neoplasms.
antineoplastic agent  A substance that inhibits or prevents the proliferation of neoplasms.
ChEBI Ontology
Outgoing Relation(s)
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 Relation(s)
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  Source
MethylselenocysteineChemIDplus
methyl-L-selenocysteineChEBI
Selenium methyl cysteineChemIDplus
Selenium-methylselenocystineChemIDplus
SelenohomocysteineChemIDplus
SelenomethylselenocysteineChemIDplus
Manual XrefsDatabases
C05689KEGG COMPOUND
Registry NumbersSources
Beilstein:2636762Beilstein
CAS:2574-71-2KEGG COMPOUND
CAS:2574-71-2ChemIDplus
CAS:26046-90-2ChemIDplus