CHEBI:27812 - Se-methyl-L-selenocysteine

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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 No supplier information found for this compound. Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search 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 ) 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