CHEBI:140298 - glutaurine zwitterion

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ChEBI Name glutaurine zwitterion
ChEBI ID CHEBI:140298
Definition A dipeptide zwitterion that is glutaurine in which a proton has been transferred from the carboxy group to the α-amino group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
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)[NH3+])=O)(O)(=O)=O
Roles Classification
Biological Role(s): 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.
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.
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ChEBI Ontology
Outgoing glutaurine zwitterion (CHEBI:140298) has role anticonvulsant (CHEBI:35623)
glutaurine zwitterion (CHEBI:140298) has role anxiolytic drug (CHEBI:35474)
glutaurine zwitterion (CHEBI:140298) has role hormone (CHEBI:24621)
glutaurine zwitterion (CHEBI:140298) is a dipeptide zwitterion (CHEBI:90799)
glutaurine zwitterion (CHEBI:140298) is conjugate acid of glutaurine(1−) (CHEBI:140299)
glutaurine zwitterion (CHEBI:140298) is tautomer of glutaurine (CHEBI:27694)
Incoming glutaurine(1−) (CHEBI:140299) is conjugate base of glutaurine zwitterion (CHEBI:140298)
glutaurine (CHEBI:27694) is tautomer of glutaurine zwitterion (CHEBI:140298)
IUPAC Name
(2S)-2-azaniumyl-5-oxo-5-[(2-sulfoethyl)amino]pentanoate
Last Modified
01 March 2018