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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:27891 -
S
-sulfo-
L
-cysteine
Main
ChEBI Ontology
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ChEBI Name
S
-sulfo-
L
-cysteine
ChEBI ID
CHEBI:27891
ChEBI ASCII Name
S-sulfo-L-cysteine
Definition
An
S
-substituted
L
-cysteine where the
S
-substituent is specified as a sulfo group.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:22075, CHEBI:8974
Supplier Information
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Molfile
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Formula
C3H7NO5S2
Net Charge
0
Average Mass
201.22100
Monoisotopic Mass
200.97656
InChI
InChI=1S/C3H7NO5S2/c4-2(3(5)6)1-10-11(7,8)9/h2H,1,4H2,(H,5,6)(H,7,8,9)/t2-/m0/s1
InChIKey
NOKPBJYHPHHWAN-REOHCLBHSA-N
SMILES
N[C@@H](CSS(O)(=O)=O)C(O)=O
Roles Classification
Chemical Role
(s):
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Br
o
nsted acid).
(via
organic amino compound
)
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
Biological Role
(s):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
S
-sulfo-
L
-cysteine (
CHEBI:27891
)
has role
human metabolite (
CHEBI:77746
)
S
-sulfo-
L
-cysteine (
CHEBI:27891
)
has role
plant metabolite (
CHEBI:76924
)
S
-sulfo-
L
-cysteine (
CHEBI:27891
)
is a
S
-substituted
L
-cysteine (
CHEBI:47910
)
S
-sulfo-
L
-cysteine (
CHEBI:27891
)
is a
organic thiosulfate (
CHEBI:37996
)
S
-sulfo-
L
-cysteine (
CHEBI:27891
)
is conjugate acid of
S
-sulfo-
L
-cysteinate(1−) (
CHEBI:62225
)
Incoming
S
-sulfo-
L
-cysteinate(1−) (
CHEBI:62225
)
is conjugate base of
S
-sulfo-
L
-cysteine (
CHEBI:27891
)
IUPAC Name
3-(sulfosulfanyl)-
L
-alanine
Synonyms
Sources
Cysteine-S-sulfate
ChemIDplus
Cysteine-S-sulfonate
ChemIDplus
Cysteinyl-S-sulfonate
ChemIDplus
Cysteinyl-S-sulfonic acid
ChemIDplus
L-Cysteine hydrogen sulfate
ChemIDplus
L
-cysteine
S
-sulfate
ChEBI
S-Sulfo-L-cysteine
KEGG COMPOUND
S
-sulfocysteine
ChEBI
S-Sulfocysteine
ChemIDplus
S
-sulpho-
L
-cysteine
ChEBI
S-Sulphocysteine
ChemIDplus
Manual Xrefs
Databases
C05824
KEGG COMPOUND
CSU
PDBeChem
View more database links
Registry Numbers
Types
Sources
1637-71-4
CAS Registry Number
KEGG COMPOUND
1637-71-4
CAS Registry Number
ChemIDplus
1726832
Reaxys Registry Number
Reaxys
Citations
Types
Sources
20179139
PubMed citation
Europe PMC
23392866
PubMed citation
Europe PMC
23430915
PubMed citation
Europe PMC
24285094
PubMed citation
Europe PMC
962465
PubMed citation
Europe PMC
Last Modified
23 October 2015