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 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