CHEBI:27694 - glutaurine

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ChEBI Name glutaurine
ChEBI ID CHEBI:27694
Definition A dipeptide resulting from the formal condensation of the amino group of taurine with the γ-carboxy group of L-glutamic acid. It was initially found in the parathyroid in 1980 and later in the brain of mammals.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:2059, CHEBI:20571
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Formula C7H14N2O6S
Net Charge 0
Average Mass 254.262
Monoisotopic Mass 254.05726
InChI InChI=1S/C7H14N2O6S/c8-5(7(11)12)1-2-6(10)9-3-4-16(13,14)15/h5H,1-4,8H2,(H,9,10)(H,11,12)(H,13,14,15)/t5-/m0/s1
InChIKey WGXUDTHMEITUBO-YFKPBYRVSA-N
SMILES S(CCNC(CC[C@@H](C(O)=O)N)=O)(O)(=O)=O
Metabolite of Species Details
Mus musculus (NCBI:txidtxid10090) Source: BioModels - MODEL1507180067 See: PubMed
Roles Classification
Chemical Role(s): inorganic acid
A Bronsted acid derived from one or more inorganic compounds. Inorganic acids (also known as mineral acids) form hydrons and conjugate base ions when dissolved in water.
(via chalcogen oxoacid )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): mammalian metabolite
Any animal metabolite produced during a metabolic reaction in mammals.
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
hormone
Originally referring to an endogenous compound that is formed in specialized organ or group of cells and carried to another organ or group of cells, in the same organism, upon which it has a specific regulatory function, the term is now commonly used to include non-endogenous, semi-synthetic and fully synthetic analogues of such compounds.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
Application(s): anticonvulsant
A drug used to prevent seizures or reduce their severity.
anxiolytic drug
Anxiolytic drugs are agents that alleviate anxiety, tension, and anxiety disorders, promote sedation, and have a calming effect without affecting clarity of consciousness or neurologic conditions.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing glutaurine (CHEBI:27694) has functional parent taurine (CHEBI:15891)
glutaurine (CHEBI:27694) has role anticonvulsant (CHEBI:35623)
glutaurine (CHEBI:27694) has role anxiolytic drug (CHEBI:35474)
glutaurine (CHEBI:27694) has role hormone (CHEBI:24621)
glutaurine (CHEBI:27694) has role human metabolite (CHEBI:77746)
glutaurine (CHEBI:27694) has role mammalian metabolite (CHEBI:75768)
glutaurine (CHEBI:27694) has role mouse metabolite (CHEBI:75771)
glutaurine (CHEBI:27694) is a L-glutamine derivative (CHEBI:24317)
glutaurine (CHEBI:27694) is a dipeptide (CHEBI:46761)
glutaurine (CHEBI:27694) is a sulfonic acid (CHEBI:29214)
glutaurine (CHEBI:27694) is tautomer of glutaurine zwitterion (CHEBI:140298)
Incoming glutaurine zwitterion (CHEBI:140298) is tautomer of glutaurine (CHEBI:27694)
IUPAC Name
N-(2-sulfoethyl)-L-glutamine
INNs Sources
glutaurina ChemIDplus
glutaurine ChemIDplus
glutaurine WHO MedNet
glutaurinum ChemIDplus
Synonyms Sources
5-glutamyl-taurine KEGG COMPOUND
5-L-glutamyl-taurine KEGG COMPOUND
γ-glutamyltaurine ChemIDplus
γ-GT ChEBI
γ-L-glutamyltaurine ChemIDplus
Brand Name Source
Litoralon ChemIDplus
Manual Xrefs Databases
C05844 KEGG COMPOUND
FDB023332 FooDB
Glutaurine Wikipedia
HMDB0004195 HMDB
View more database links
Registry Number Type Source
56488-60-9 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
1450962 PubMed citation Europe PMC
157672 PubMed citation Europe PMC
15838590 PubMed citation Europe PMC
2875599 PubMed citation Europe PMC
3185869 PubMed citation Europe PMC
3561723 PubMed citation Europe PMC
3705977 PubMed citation Europe PMC
3739747 PubMed citation Europe PMC
6775940 PubMed citation Europe PMC
7161962 PubMed citation Europe PMC
7428713 PubMed citation Europe PMC
7446224 PubMed citation Europe PMC
7909918 PubMed citation Europe PMC
8915385 PubMed citation Europe PMC
Last Modified
01 March 2018