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Substance
ID:1845456
Structure
Similarity
Functional Group
Text
ID:63381
pazopanib
Chemical Entities of Biological Interest
ID: CHEBI:71219
Names and Identifiers
IUPAC name
5-({4-[(2,3-dimethyl-2H-indazol-6-yl)(methyl)amino]pyrimidin-2-yl}amino)-2-methylbenzene-1-sulfonamide
IUPAC Traditional name
pazopanib
Synonyms
pazopanib
GW 78603
GW786034
International Nonproprietary Name (INN)
pazopanib
pazopanibum
Registration numbers
CAS Number
444731-52-6
PubChem CID
10113978
LINCS Database
LSM-1114
PubMed Citation Links
22917595
22341567
22830347
22112314
22359392
22733795
22688250
22233389
22190407
23064954
23072642
22861374
21766486
22733110
22679111
23054212
23135778
21394443
22766517
21811833
22984765
22595799
23088634
22759480
22716487
Reaxys Registry
11646488
ACToR Database
444731-52-6
790713-33-6
BKMS React Database
155472
BRENDA Database
2.4.1.17
2.7.10.1
BRENDA Ligand Database
155472
CHEMBL
CHEMBL477772
CompTox Database
DTXSID8048733
MetaboLights Database
MTBLS3950
SureChEMBL Database
SCHEMBL588608
Wikipedia Title
Pazopanib
Patent number
WO2007064753
US2008293691
WO2006020564
WO2007143483
WO2011058179
WO2011069053
WO2012106302
WO2011150044
Drug Central Database
4,118
BindingDB Database
26474
Reactom Database
R-HSA-2029992
R-HSA-2077424
R-HSA-389083
R-HSA-5213464
R-HSA-5213466
R-HSA-9674093
R-HSA-9674427
R-HSA-9693978
CHEBI ID
CHEBI:71219
PubChem SID
160646127
Properties
No Data Available
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Molecule Details
A pyrimidine that is 5-(pyrimidin-2-yl}amino-2-methylbenzenesulfonamide substituted at position 4 by a (2,3-dimethylindazol-6-yl)(methyl)amino group. Used as its hydrochloride salt for treatment of kidney cancer.
Molecular Spectra
No Data Available
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References
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Molecular Spectra
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