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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:35494 -
D
-cystine
Main
ChEBI Ontology
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ChEBI Name
D
-cystine
ChEBI ID
CHEBI:35494
ChEBI ASCII Name
D-cystine
Definition
The
D
-enantiomer of cystine.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C6H12N2O4S2
Net Charge
0
Average Mass
240.30256
Monoisotopic Mass
240.02385
InChI
InChI=1S/C6H12N2O4S2/c7-
3(5(9)
10)
1-
13-
14-
2-
4(8)
6(11)
12/h3-
4H,1-
2,7-
8H2,(H,9,10)
(H,11,12)
/t3-
,4-
/m1/s1
InChIKey
LEVWYRKDKASIDU-QWWZWVQMSA-N
SMILES
N[C@H](CSSC[C@@H](N)C(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):
EC 1.2.1.11 (aspartate-semialdehyde dehydrogenase) inhibitor
Any EC 1.2.1.* (oxidoreductase acting on donor aldehyde/oxo group with NAD
+
or NADP
+
as acceptor) inhibitor that inhibits the action of aspartate-semialdehyde dehydrogenase (EC 1.2.1.11).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
(via
cystine
)
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
(via
cystine
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
D
-cystine (
CHEBI:35494
)
has role
EC 1.2.1.11 (aspartate-semialdehyde dehydrogenase) inhibitor (
CHEBI:145814
)
D
-cystine (
CHEBI:35494
)
is a
cystine (
CHEBI:17376
)
D
-cystine (
CHEBI:35494
)
is enantiomer of
L
-cystine (
CHEBI:16283
)
D
-cystine (
CHEBI:35494
)
is tautomer of
D
-cystine zwitterion (
CHEBI:145813
)
Incoming
L
-cystine (
CHEBI:16283
)
is enantiomer of
D
-cystine (
CHEBI:35494
)
D
-cystine residue (
CHEBI:50065
)
is substituent group from
D
-cystine (
CHEBI:35494
)
D
-cystyl group (
CHEBI:50049
)
is substituent group from
D
-cystine (
CHEBI:35494
)
D
-cystine zwitterion (
CHEBI:145813
)
is tautomer of
D
-cystine (
CHEBI:35494
)
IUPAC Names
(2
S
,2'
S
)-3,3'-disulfanediylbis(2-aminopropanoic acid)
D
-cystine
Synonyms
Sources
(2
S
,2'
S
)-3,3'-dithiobis(2-aminopropanoic acid)
ChEBI
cystine
D
-form
ChemIDplus
Registry Numbers
Types
Sources
1728093
Reaxys Registry Number
Reaxys
1728093
Beilstein Registry Number
Beilstein
349-46-2
CAS Registry Number
ChemIDplus
Citations
Types
Sources
14726201
PubMed citation
Europe PMC
16782275
PubMed citation
Europe PMC
20800236
PubMed citation
Europe PMC
674038
PubMed citation
Europe PMC
Last Modified
16 January 2020