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Substance
ID:1826061
Structure
Similarity
Functional Group
Text
ID:166
lidocaine
Chemical Entities of Biological Interest
ID: CHEBI:6456
Names and Identifiers
IUPAC name
2-(diethylamino)-N-(2,6-dimethylphenyl)acetamide
Brand Name
Lidoderm
IUPAC Traditional name
lidocaine
Synonyms
lidocaine
2-(Diethylamino)-2',6'-acetoxylidide
2-(Diethylamino)-N-(2,6-dimethylphenyl)acetamide
Lidocaine
alpha-diethylamino-2,6-dimethylacetanilide
Registration numbers
CAS Number
137-58-6
PubChem CID
3676
DrugBank ID
DB00281
Wikipedia Title
Lidocaine
KEGG ID
C07073
LINCS Database
LSM-3165
PubMed Citation Links
11120381
11106996
18940244
11692349
15056998
16668583
17214917
11431418
Reaxys Registry
2215784
ACToR Database
137-58-6
BKMS React Database
100862
229618
9617
229619
146897
BRENDA Database
1.1.1.49
1.3.1.2
3.1.1.7
7.2.2.10
2.3.1.26
2.7.11.24
1.14.13.8
7.6.2.2
2.8.2.1
1.11.2.1
3.1.1.1
BRENDA Ligand Database
229618
229619
146897
9617
100862
CHEMBL
CHEMBL79
CompTox Database
DTXSID1045166
MetaboLights Database
MTBLS4967
MTBLS591
MTBLS4366
MTBLS615
MTBLS690
MTBLS2406
MTBLS2394
MTBLS1051
MTBLS136
MTBLS1411
MTBLS1267
MTBLS1326
MTBLS1757
MTBLS205
MTBLS204
MTBLS407
MTBLS2295
MTBLS179
Protein Data Bank
3jqz
3ttr
SureChEMBL Database
SCHEMBL17967359
SCHEMBL15689
UniProt Database
O08966
Q863T6
O77504
Q63089
A7MBE0
O15245
Q7NDN8
Beilstein Number
2215784
HMDB Database
HMDB0014426
MassBank Database
EA257201
EA257202
EA257203
EA257204
EA257205
EA257206
EA257207
EA257208
EA257209
EA257210
EA257211
EA257212
EA257213
EA257214
Patent number
EP1488789
EP1514539
EP1559418
EP1576953
EP1586347
EP1586349
EP1629852
EP1637132
EP1639994
EP1685843
EP1700616
EP1702597
EP1710256
EP1716868
EP1731142
EP1743635
EP1762226
EP1764111
EP1772767
EP1779898
EP1782831
EP1782860
EP1785145
EP1813285
EP1813295
EP1815845
EP1815846
EP1829527
EP1829528
EP1834627
EP1839648
EP1842858
EP1849463
EP1891945
EP1902705
US2002115655
EP1925316
EP1949895
EP1955707
EP1972684
EP1990639
US2004068007
US2004151763
US2004254182
US2005233398
US2006079558
US2006079559
US2007184020
US2007189977
US2007189978
US2007191365
US2007196323
US2007196452
EP0826685
EP1405646
EP1438962
US2007196453
US2007196914
US2007197456
US2007202051
US2007203079
US2007207193
US2007207222
US2007219170
US2007219185
US2007231274
US2007238674
US2007248654
US2007248658
US2007248677
US2007258894
US2007258939
US2008221161
US2008221206
US2008234257
US2008268071
US7261903
US7273887
WO2005020894
WO2005120148
WO2006036936
WO2006037047
WO2007087624
WO2007089902
WO2007098408
WO2007100902
WO2007103555
WO2007103687
WO2007104011
WO2007106457
WO2007110871
WO2007111720
WO2007112581
WO2007117352
WO2007117621
WO2007125545
WO2007128349
WO2007136707
WO2008140859
EP1762236
Drug Central Database
1,579
BindingDB Database
50017662
KEGG DRUG Database
D00358
VSDB Database
1,903
IEDB Database
116205
CHEBI ID
CHEBI:6456
PubChem SID
26744219
Properties
No Data Available
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Molecule Details
The monocarboxylic acid amide resulting from the formal condensation of N,N-diethylglycine with 2,6-dimethylaniline.
Molecular Spectra
No Data Available
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References
No Data Available
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Names and Identifiers
Registration numbers
Properties
Molecule Details
Molecular Spectra
References