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Substance
ID:1825995
Structure
Similarity
Functional Group
Text
ID:827
isoniazide
Chemical Entities of Biological Interest
ID: CHEBI:6030
Names and Identifiers
IUPAC Traditional name
isoniazid
IUPAC name
pyridine-4-carbohydrazide
Synonyms
isoniazide
4-pyridinecarbohydrazide
Isoniazid
Isonicotinsaeurehydrazid
isoniazid
isonicotinic acid hydrazide
isonicotinic hydrazide
isonicotinohydrazide
isonicotinoylhydrazide
pyridine-4-carboxylic acid hydrazide
Registration numbers
CAS Number
54-85-3
Beilstein Number
119374
PubChem CID
3767
DrugBank ID
DB00951
Wikipedia Title
Isoniazid
KEGG ID
C07054
LINCS Database
LSM-6682
MetaCyc Database
ISONIAZIDE
PubMed Citation Links
15013786
445303
18220565
19183459
Reaxys Registry
119374
ACToR Database
37271-10-6
54-85-3
BKMS React Database
51707
208021
BRENDA Database
5.1.1.11
2.3.2.7
6.3.2.1
1.14.13.8
2.4.2.30
1.11.2.2
4.1.1.15
4.1.1.17
4.1.1.50
4.1.1.57
4.1.1.65
5.1.1.7
5.4.3.3
5.4.99.5
4.4.1.1
3.2.2.5
4.3.1.19
3.5.1.19
1.1.1.14
1.17.1.9
3.2.2.6
1.3.1.44
1.3.1.9
1.4.3.13
1.4.3.8
1.5.1.3
2.2.1.6
1.4.9.1
1.4.9.2
1.13.12.3
2.3.1.35
2.3.1.37
2.3.1.39
2.3.1.47
5.1.1.17
2.6.1.7
2.6.1.57
2.6.1.45
2.6.1.2
2.4.1.18
2.6.1.58
2.6.1.63
2.6.1.60
2.6.1.62
2.6.1.13
2.4.2.8
2.6.1.1
2.6.1.15
2.6.1.4
2.6.1.43
2.6.1.44
2.6.1.51
2.6.1.64
2.7.1.35
2.3.1.180
1.4.3.21
1.4.3.22
1.5.3.17
1.5.3.16
1.11.1.21
1.1.98.3
1.3.1.118
2.3.1.5
2.3.1.118
3.4.22.6
1.11.1.5
1.11.1.6
BRENDA Ligand Database
208021
51707
CHEMBL
CHEMBL64
CompTox Database
DTXSID8020755
MetaboLights Database
MTBLS606
MTBLS601
MTBLS615
MTBLS926
MTBLS867
MTBLS2878
MTBLS2945
MTBLS379
Protein Data Bank
5ksn
3wxo
4pae
5ksg
5kt8
5sxq
5sxs
5sxt
5syi
5syj
6cdq
6cfq
SABIO-RK Database
14461
15154
12151
6691
SureChEMBL Database
SCHEMBL228
UniProt Database
P9WF09
P9WJ98
P9WJ99
P9WJ96
P9WJ97
P9WJ94
P9WJ95
P0A5Y7
P42829
P9WGR1
Q9XBQ8
P9WQB7
P84887
P84888
P9WJI5
P05181
P50294
Q939D2
A0QXX7
A0R609
A5U3S7
P9WIE4
P9WIE5
P73911
A0R1V9
P9WQB6
Q7D5T7
P9WNX1
P0A5L9
O86309
P9WJI4
NMRShiftDB Database
20097187
Patent number
WO2006023231
WO2006082010
WO2008121670
WO2008151303
EP1690549
EP1752143
EP1754712
EP1803463
EP1839648
EP1884520
US2002048798
US2003096870
US2003105066
US2003114531
US2003207815
US2004198669
US2005009870
US2005014786
US2005080087
US2007184076
US2007190067
US2007202051
US2007219221
US2007248569
US2007259053
US2007269501
US2007269539
WO2005007628
WO2005016286
WO2005037199
WO2005063761
WO2005063762
WO2006005137
WO2007086039
WO2007092416
WO2007100206
WO2007106450
WO2007117509
WO2007117550
WO2007118329
WO2007133803
WO2008117079
EP1031570
US2003028026
WO2008127640
EP1832575
WO2007121963
EP0933375
EP1085021
EP1356813
EP1757314
EP1760078
GB2258233
GB2368843
US2002110535
US2002127577
US2004022856
US2004037802
US2004091426
US2005181393
US2005209176
US2005233389
US2005250214
US2006079542
US2006121530
US2006252107
US2006286647
US2007166276
WO2005012579
WO2005016874
WO2005054234
WO2006005112
WO2006007532
EnzymePortal Database
P84887
P84888
Drug Central Database
1,497
BindingDB Database
50336507
KEGG DRUG Database
D00346
Reactom Database
R-HSA-174967
Gmelin ID
82804
CHEBI ID
CHEBI:6030
PubChem SID
8145964
Properties
No Data Available
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Molecule Details
A carbohydrazide obtained by formal condensation between pyridine-4-carboxylic acid and hydrazine.
Molecular Spectra
No Data Available
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References
No Data Available
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