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Substance
ID:1826724
Structure
Similarity
Functional Group
Text
ID:62
valsartan
Chemical Entities of Biological Interest
ID: CHEBI:9927
Names and Identifiers
IUPAC Traditional name
diovan
IUPAC name
(2S)-3-methyl-2-(N-{[2'-(1H-1,2,3,4-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl]methyl}pentanamido)butanoic acid
Synonyms
valsartan
(S)-N-valeryl-N-{[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]-methyl}-valine
Diovan
N-(p-(o-1H-tetrazol-5-ylphenyl)benzyl)-N-valeryl-L-valine
N-pentanoyl-N-{[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl}-L-valine
International Nonproprietary Name (INN)
valsartan
Registration numbers
CAS Number
137862-53-4
PubChem CID
60846
DrugBank ID
DB00177
LINCS Database
LSM-2993
Reaxys Registry
7754038
CHEMBL
CHEMBL1069
MetaboLights Database
MTBLS1455
MTBLS136
MTBLS204
MTBLS407
MTBLS220
MTBLS2633
Protein Data Bank
7bm1
SureChEMBL Database
SCHEMBL2542
Beilstein Number
7754038
HMDB Database
HMDB0014323
Wikipedia Title
Valsartan
MassBank Database
EA258301
EA258302
EA258303
EA258304
EA258305
EA258306
EA258307
EA258308
EA258309
EA258310
EA258311
EA258312
EA258313
EA258314
EA258351
EA258352
EA258353
EA258354
EA258355
EA258356
EA258358
EA258359
EA258360
EA258361
EA258362
EA258364
Patent number
EP1930000
EP1939188
EP1950204
EP1980249
EP1982711
EP1990049
EP1994926
US2004147575
US2005009870
US2005014786
US2005043325
US2005059655
US2005059827
US2005065209
US2005080087
US2005085497
US2005101652
US2005119312
US2005124624
US2005124661
US2005131038
US2005137216
US2005154038
US2005165075
US2005176749
US2005182110
US2005187267
US2005222233
US2006100443
US2006135511
US2006148790
US2006154962
US2006154975
US2006173059
US2006189598
US2006189603
US2006194868
US2006270701
US2006281801
US2007037821
US2007185056
US2007191371
US2007191438
US2007191446
US2007203155
US2007203157
US2007203211
US2007213390
US2007225323
US2007231386
US2007232648
US2007238674
US2007238740
US2007244130
US2007249583
US2007259890
US2007264334
US2007270412
US2007270453
US2008161372
US2008194565
US2008255036
US2008261959
US2008262059
US2008262086
US2008275093
US2008275096
US2008279932
US2008287407
US2008292608
US2008293678
US2008293701
US2008293702
US2008293791
WO2005000807
WO2005007628
WO2005013894
WO2005014602
WO2005016286
WO2005018561
WO2005021535
WO2005023183
WO2005030135
WO2005030758
WO2005037199
WO2005049586
WO2005049587
WO2005049588
WO2005049616
WO2005051386
WO2005051928
WO2005051929
WO2005060603
WO2005063761
WO2005063762
WO2005070207
WO2005072132
WO2005072729
WO2005072732
WO2005073203
WO2005073221
WO2005077925
WO2005102987
WO2005105096
WO2005113506
WO2005113519
WO2005116000
WO2005116016
WO2006031610
EP1106210
EP1197226
EP1329218
EP1356815
EP1514543
EP1533305
EP1553091
EP1559424
EP1579862
EP1579872
EP1588706
EP1611886
EP1627638
EP1629835
EP1661891
EP1671632
EP1674080
EP1714651
EP1714963
EP1723962
EP1746099
EP1774967
EP1776953
EP1776954
EP1787647
EP1790353
EP1849777
EP1862181
EP1867342
EP1870098
EP1872797
EP1884513
EP1889847
EP1894567
EP1897537
EP1908469
EP1925303
WO2006031676
WO2006055542
WO2006058701
WO2006067216
WO2006076509
WO2006076561
WO2006078593
WO2006078995
WO2006083779
WO2006083924
WO2006084176
WO2006090235
WO2006091716
WO2006093864
WO2006098705
WO2006099058
WO2006102071
WO2006103068
WO2006112772
WO2006116157
WO2006136402
WO2007085399
WO2007086078
WO2007087448
WO2007089557
WO2007089667
WO2007089745
WO2007092270
WO2007092469
WO2007093021
WO2007098387
WO2007098390
WO2007111958
WO2007112288
WO2007113226
WO2007115821
WO2007115822
WO2007117559
WO2007117560
WO2007117621
WO2007120523
WO2007123718
WO2007128349
WO2008122020
WO2008122787
WO2008128647
WO2008135762
WO2008138871
WO2008138912
WO2008148599
WO2008156816
Drug Central Database
2,806
BindingDB Database
50049186
KEGG DRUG Database
D00400
Reactom Database
R-HSA-374173
R-HSA-9615249
CHEBI ID
CHEBI:9927
PubChem SID
46530915
Properties
No Data Available
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Molecule Details
A monocarboxylic acid amide consisting of L-valine in which the amino hydrogens have been replaced by a pentanoyl and a [2'-(1H-tetrazol-5-yl)biphenyl]-4-yl]methyl group. It exhibits antihypertensive activity.
Molecular Spectra
No Data Available
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References
No Data Available
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