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> Main
CHEBI:16668 - hypotaurine
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ChEBI Name
hypotaurine
ChEBI ID
CHEBI:16668
Definition
An aminosulfinic acid comprising ethylamine having the sulfo group at the 2-position.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:5839, CHEBI:14429, CHEBI:24760
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Formula
C2H7NO2S
Net Charge
0
Average Mass
109.14852
Monoisotopic Mass
109.01975
InChI
InChI=1S/C2H7NO2S/c3-1-2-6(4)5/h1-3H2,(H,4,5)
InChIKey
VVIUBCNYACGLLV-UHFFFAOYSA-N
SMILES
NCCS(O)=O
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
Source: BioModels - MODEL1507180067 See:
PubMed
Homo sapiens
(NCBI:txid9606)
See:
DOI
Roles Classification
Biological Role
(s):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
hypotaurine (
CHEBI:16668
)
has role
human metabolite (
CHEBI:77746
)
hypotaurine (
CHEBI:16668
)
has role
metabolite (
CHEBI:25212
)
hypotaurine (
CHEBI:16668
)
has role
mouse metabolite (
CHEBI:75771
)
hypotaurine (
CHEBI:16668
)
is a
aminosulfinic acid (
CHEBI:37794
)
hypotaurine (
CHEBI:16668
)
is conjugate acid of
hypotaurine(1−) (
CHEBI:140741
)
hypotaurine (
CHEBI:16668
)
is tautomer of
hypotaurine zwitterion (
CHEBI:57853
)
Incoming
hypotaurocyamine (
CHEBI:16209
)
has functional parent
hypotaurine (
CHEBI:16668
)
hypotaurine(1−) (
CHEBI:140741
)
is conjugate base of
hypotaurine (
CHEBI:16668
)
hypotaurine zwitterion (
CHEBI:57853
)
is tautomer of
hypotaurine (
CHEBI:16668
)
IUPAC Name
2-aminoethanesulfinic acid
Synonyms
Sources
2-Aminoethanesulfinic acid
KEGG COMPOUND
Hypotaurine
KEGG COMPOUND
Manual Xrefs
Databases
C00519
KEGG COMPOUND
HMDB0000965
HMDB
Hypotaurine
Wikipedia
HYPOTAURINE
MetaCyc
View more database links
Registry Numbers
Types
Sources
1743127
Reaxys Registry Number
Reaxys
300-84-5
CAS Registry Number
ChemIDplus
Citation
Type
Source
22735334
PubMed citation
Europe PMC
Last Modified
02 April 2019