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ID:1825778
Structure
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Functional Group
Text
ID:491
ethionamide
Chemical Entities of Biological Interest
ID: CHEBI:4885
Names and Identifiers
IUPAC Traditional name
ethionamide
IUPAC name
2-ethylpyridine-4-carbothioamide
Brand Name
Trecator
Synonyms
ethionamide
2-ethyl-4-thiopyridylamide
ETH
ETP
Ethinamide
Ethionamide
Ethioniamide
Ethylisothiamide
Ethyonomide
Etionamid
Etionamide
Etioniamid
ethionamide
International Nonproprietary Name (INN)
ethionamidum
etionamida
Registration numbers
PubChem CID
2761171
CAS Number
536-33-4
Wikipedia Title
Ethionamide
DrugBank ID
DB00609
KEGG ID
C07665
LINCS Database
LSM-5620
PubMed Citation Links
14651620
15673755
15850780
Reaxys Registry
116474
ACToR Database
5261-38-1
536-33-4
BKMS React Database
156877
BRENDA Database
1.14.13.148
3.1.1.7
1.3.1.9
2.3.1.180
1.3.1.118
1.14.13.92
1.14.13.8
BRENDA Ligand Database
156877
CHEMBL
CHEMBL1441
CompTox Database
DTXSID0020577
MetaboLights Database
MTBLS867
MTBLS2406
MTBLS379
SABIO-RK Database
8081
SureChEMBL Database
SCHEMBL27007
UniProt Database
P9WJ99
P0A5Y7
P42829
P9WGR1
P46979
Q7TVI1
A0R666
P9WMC0
P9WMC1
P0ACZ3
P0ACZ2
P9WNF9
P9WJ97
P9WJ95
O82882
A0R665
P9WNF8
P58764
Q8XC28
P38134
Q7TVI2
Rhea Database
RHEA:47616
Beilstein Number
116474
HMDB Database
HMDB0014747
NMRShiftDB Database
20208897
Patent number
WO2007127908
US2007219221
EP1884520
US2003105066
US2007196504
US2007231390
US2007265319
US2007269539
WO2007117509
WO2007117550
WO2007133803
EP0839810
EP0942051
EP1911350
US2003207895
US2004072310
US2004235023
US2005038011
US2005096484
US2006004084
US2006058317
US2006116386
US2006160865
US2006194785
US2006286647
US2008279917
US2008287474
WO2005039587
WO2005095403
WO2006014087
WO2006043090
WO2006118955
WO2006135993
WO2008112280
WO2005079866
Drug Central Database
1,083
BindingDB Database
50239976
KEGG DRUG Database
D00591
CHEBI ID
CHEBI:4885
PubChem SID
50139237
Properties
No Data Available
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Molecule Details
A thiocarboxamide that is pyridine-4-carbothioamide substituted by an ethyl group at position 2. A prodrug that undergoes metabolic activation by conversion to the corresponding S-oxide.
Molecular Spectra
No Data Available
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References
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