CHEBI:64243 - monosodium L-glutamate

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ChEBI Name monosodium L-glutamate ChEBI ID CHEBI:64243 ChEBI ASCII Name monosodium L-glutamate Definition An optically active form of monosodium glutamate having L-configuration. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Wikipedia License Read full article at Wikipedia Formula C5H8NNaO4 Net Charge 0 Average Mass 169.11110 Monoisotopic Mass 169.03510 InChI InChI=1S/C5H9NO4.Na/c6-3(5(9)10)1-2-4(7)8;/h3H,1-2,6H2,(H,7,8)(H,9,10);/q;+1/p-1/t3-;/m0./s1 InChIKey LPUQAYUQRXPFSQ-DFWYDOINSA-M SMILES [Na+].[NH3+][C@@H](CCC([O-])=O)C([O-])=O Roles Classification Biological Role(s): flavouring agent A food additive that is used to added improve the taste or odour of a food. Application(s): flavouring agent A food additive that is used to added improve the taste or odour of a food. View more via ChEBI Ontology ChEBI Ontology Outgoing monosodium L-glutamate (CHEBI:64243) has part L-glutamate(1−) (CHEBI:29985) monosodium L-glutamate (CHEBI:64243) has role flavouring agent (CHEBI:35617) monosodium L-glutamate (CHEBI:64243) is a monosodium glutamate (CHEBI:64220) monosodium L-glutamate (CHEBI:64243) is enantiomer of monosodium D-glutamate (CHEBI:64244) Incoming monosodium D-glutamate (CHEBI:64244) is enantiomer of monosodium L-glutamate (CHEBI:64243) IUPAC Name sodium (2S)-2-azaniumylpentanedioate Synonyms Sources Glutamate monosodium salt ChemIDplus Glutamate Sodium ChemIDplus Glutamic acid, monosodium salt ChemIDplus Glutammato monosodico ChemIDplus L(+) Sodium glutamate ChemIDplus Monosodioglutammato ChemIDplus Monosodium glutamate ChemIDplus MSG ChemIDplus Natrium L-hydrogenglutamat ChemIDplus Natriumglutaminat ChemIDplus sodium (2S)-2-ammoniopentanedioate IUPAC Sodium glutamate ChemIDplus Sodium hydrogen glutamate ChemIDplus Sodium L-glutamate ChemIDplus Manual Xref Database Monosodium_glutamate Wikipedia View more database links Registry Numbers Types Sources 142-47-2 CAS Registry Number ChemIDplus 17456768 Reaxys Registry Number Reaxys Citations Types Sources 21054690 PubMed citation Europe PMC 21925279 PubMed citation Europe PMC 22008743 PubMed citation Europe PMC 22104770 PubMed citation Europe PMC 22154980 PubMed citation Europe PMC 22204889 PubMed citation Europe PMC 22222358 PubMed citation Europe PMC 22223845 PubMed citation Europe PMC 22245354 PubMed citation Europe PMC 22248457 PubMed citation Europe PMC 22286833 PubMed citation Europe PMC 22293291 PubMed citation Europe PMC 22307498 PubMed citation Europe PMC 22346139 PubMed citation Europe PMC 22415589 PubMed citation Europe PMC Last Modified 20 February 2013