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Substance
ID:1820738
Structure
Similarity
Functional Group
Text
ID:58694
cystathionine
Chemical Entities of Biological Interest
ID: CHEBI:17755
Names and Identifiers
IUPAC name
2-amino-4-[(2-amino-2-carboxyethyl)sulfanyl]butanoic acid
IUPAC Traditional name
cystathionine
Synonyms
cystathionine
Cystathionine
DL-Cystathionine
cystathione
Registration numbers
PubChem CID
834
CAS Number
535-34-2
KEGG ID
C00542
PubMed Citation Links
22264337
15033753
12907234
22212096
Reaxys Registry
2416815
ACToR Database
14545-37-0
30651-43-5
535-35-3
535-34-2
BKMS React Database
95435
22107
91102
91642
97906
90821
94499
96521
BRENDA Database
2.5.1.49
7.4.2.12
4.4.1.1
4.3.1.19
BRENDA Ligand Database
90821
96521
97906
91102
91642
95435
94499
22107
CHEMBL
CHEMBL209241
CompTox Database
DTXSID50861587
MetaboLights Database
MTBLS444
MTBLS5345
MTBLS606
MTBLS442
MTBLS601
MTBLS533
MTBLS615
MTBLS612
MTBLS745
MTBLS697
MTBLS899
MTBLS8
MTBLS789
MTBLS2394
MTBLS1033
MTBLS259
MTBLS121
MTBLS1221
MTBLS138
MTBLS1282
MTBLS135
MTBLS158
MTBLS159
MTBLS181
MTBLS180
MTBLS186
MTBLS1757
MTBLS205
MTBLS201
MTBLS204
MTBLS292
MTBLS3
MTBLS309
MTBLS301
MTBLS406
MTBLS3786
MTBLS38
MTBLS407
MTBLS3852
MTBLS1903
MTBLS220
MTBLS2205
MTBLS2159
MTBLS2215
MTBLS2771
SABIO-RK Database
1504
1500
SureChEMBL Database
SCHEMBL81860
UniProt Database
P53101
F4K5T2
Q58DW2
Q55DV9
P32929
Q60HG7
Q8VCN5
Q19QT7
P18757
P55216
P46794
P35520
Q58H57
Q91WT9
Q9N0V7
P32232
P32582
Q14894
P38675
O74314
P47164
P00935
P44502
Q9ZMW7
Q1M0P5
P56069
P24601
P66876
P46807
P9WGB6
P9WGB7
P53780
O31632
Q07703
Q83A83
P85217
P06721
P44527
P0A4K2
P0C2T9
A2RM21
P55217
Q52811
P18949
P43623
O31631
P22188
Q59829
P31373
P23256
Q12198
Q9YBL2
Q04533
O34406
O34852
O34315
O34931
O34900
O05394
O05393
Q08432
Q93QC6
P63503
Q9CBM9
P9WP50
P9WQ82
P9WQ83
P9WP51
Q1K8G0
O94350
Q2KHX6
Q28488
O54983
Q9QYU4
O84395
Patent number
EP1630164
US2007207956
US2008207751
WO2006024453
WO2006111791
WO2006134489
GeneOntology Database
GO:0019283
GO:0019343
GO:0019346
GO:0019279
CHEBI ID
CHEBI:17755
CHEBI:4048
CHEBI:14059
PubChem SID
8144576
Properties
No Data Available
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Molecule Details
A modified amino acid generated by enzymic means from homocysteine and serine.
Molecular Spectra
No Data Available
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References
No Data Available
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Molecular Spectra
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