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Chemical substance record

Glutaurine

56488-60-9C7H14N2O6S254.264 g/mol
Protein/Peptide SequenceChEBI source record

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. — ChEBI

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Identity & molecular properties

Source-linked values
CAS number56488-60-9ChEBI ↗
Molecular formulaC7H14N2O6SChEBI ↗
Molar mass254.264 g/molChEBI ↗
Monoisotopic mass254.05726 DaChEBI ↗
Formal charge0ChEBI ↗
ChEBI identifierCHEBI:27694ChEBI ↗

Cross-source molecular data

PubChem
Molar mass254.26 g/molPubChem ↗
Exact mass254.05725734 DaPubChem ↗
Computed XLogP-4.9PubChem ↗
Topological polar surface area (Ų)155PubChem ↗
H-bond donors4PubChem ↗
H-bond acceptors7PubChem ↗
Rotatable bonds7PubChem ↗

PubChem computed values are shown separately from the ChEBI record. An exact InChIKey match was used to connect the records. Molecular descriptors do not describe a supplied product’s purity, particle size or performance.

Names & structural identifiers

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glutaurine
N-(2-sulfoethyl)-L-glutamine
WGXUDTHMEITUBO-YFKPBYRVSA-N
N[C@@H](CCC(=O)NCCS(=O)(=O)O)C(=O)O
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

Names & synonyms

glutaurinaglutaurinumLitoralonN-(2-sulfoethyl)-L-glutamine

Names are supplied by ChEBI. Trade names and related synonyms may describe a broader product context.

Classification & relationships

ChEBI ontology

Roles recorded in ChEBI

hormoneanxiolytic druganticonvulsantmammalian metabolitemouse metabolitehuman metabolite

Database role annotations describe reported biological or chemical roles; they are not product approvals or recommendations for use.

Mass ↔ amount of substance

Calculated from sourced mass
Equivalent amount
0.00393292 mol

Uses 254.264 g/mol from ChEBI. Assumes the substance described by this record; no purity or concentration correction is applied.

Elemental composition

Theoretical mass fractions
O
Oxygen · 6 atoms
37.75%
C
Carbon · 7 atoms
33.07%
S
Sulfur · 1 atom
12.61%
N
Nitrogen · 2 atoms
11.02%
H
Hydrogen · 14 atoms
5.55%

Calculated theoretical mass fractions from the reported formula and PubChem periodic-table atomic masses. These are not assay or purity results.

Research & patent references

Selected source associations

Sources & record history

Checked 27 Sep 2026
EMBL-EBI ChEBI · CHEBI:27694

Release 255, 9 September 2026. ChEBI three-star (manually annotated) source entry. View original record ↗ · CC BY 4.0

NCBI PubChem · CID 68759 · retrieved 2026-09-27

PubCAS formats source data, connects references and computes explicitly labelled conversions. CAS cross-references are supplied by ChEBI; they do not constitute CAS verification or endorsement.