Se-methyl-L-selenocysteine (CHEBI:27812)

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CHEBI:27812 - Se-methyl-L-selenocysteine

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ChEBI ID	CHEBI:27812
ChEBI Name	Se-methyl-L-selenocysteine
Stars
ASCII Name	Se-methyl-L-selenocysteine
Definition	An L-α-amino acid compound having methylselanylmethyl as the side-chain.
Secondary ChEBI IDs	CHEBI:9067, CHEBI:22076
Last Modified	26 March 2015
Downloads	Molfile

Formula	C4H9NO2Se
Net Charge	0
Average Mass	182.081
Monoisotopic Mass	182.97985
SMILES	C[Se]C[C@H](N)C(=O)O
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

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
methylselenocysteine	ChEMBL
Methylselenocysteine	ChemIDplus
methyl-L-selenocysteine	ChEBI
Selenium methyl cysteine	ChemIDplus
Selenium-methylselenocystine	ChemIDplus
Selenohomocysteine	ChemIDplus

Manual Xrefs	Databases
C05689	KEGG COMPOUND

Registry Numbers	Sources
Beilstein:2636762	Beilstein
CAS:2574-71-2	ChemIDplus
CAS:2574-71-2	KEGG COMPOUND
CAS:26046-90-2	ChemIDplus

Citations