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Substance
ID:1823625
Structure
Similarity
Functional Group
Text
ID:266
tacrine
Chemical Entities of Biological Interest
ID: CHEBI:45980
Names and Identifiers
IUPAC name
1,2,3,4-tetrahydroacridin-9-amine
IUPAC Traditional name
tacrine
Synonyms
tacrine
1,2,3,4-tetrahydro-9-acridinamine
1,2,3,4-tetrahydro-9-aminoacridine
5-amino-6,7,8,9-tetrahydroacridine
9-amino-1,2,3,4-tetrahydroacridine
TACRINE
Tacrine
tetrahydroaminacrine
Registration numbers
PubChem CID
1935
CAS Number
321-64-2
KEGG ID
C01453
LINCS Database
LSM-5871
PubMed Citation Links
10817586
7866482
24560791
Reaxys Registry
147610
ACToR Database
321-64-2
BKMS React Database
199427
220586
1456
BRENDA Database
1.6.2.2
3.1.1.7
3.1.1.8
2.1.1.103
3.4.21.98
3.5.1.13
1.2.3.1
1.4.3.4
1.8.1.12
1.13.12.5
2.1.1.8
BRENDA Ligand Database
1456
199427
220586
CHEMBL
CHEMBL95
CompTox Database
DTXSID1037272
MetaboLights Database
MTBLS804
MTBLS2878
Protein Data Bank
1acj
1mx1
2aow
2aox
4bds
7e3i
SABIO-RK Database
7923
SureChEMBL Database
SCHEMBL2828
Beilstein Number
147610
PDBeChem Database
THA
Wikipedia Title
Tacrine
Patent number
EP1867642
EP1918286
EP1938811
US2003026850
US2003166721
US2004142904
US2004254182
US2005009870
US2005014786
US2005026946
US2005080087
US2005187267
US2005250843
US2006025345
US2006040948
US2006040994
US2007010507
US2007185145
US2007203080
US2007225379
US2007238762
US2007249612
US2007254889
US2008293680
WO2005000303
WO2005000304
WO2005007628
WO2005016286
WO2005035532
WO2005037199
WO2005063761
WO2005063762
WO2005077925
WO2005092392
WO2006014762
WO2006019673
WO2006060203
WO2006099379
WO2006135839
WO2007100902
WO2007109851
WO2007127273
WO2007127474
WO2008137139
WO2008139293
WO2008153792
WO2008153793
EP1088550
WO2007087637
EP1118322
EP1457490
EP1514542
EP1576985
EP1779867
EP1844769
EP1857817
DrugBank ID
DB00382
Drug Central Database
2,551
BindingDB Database
8961
KEGG DRUG Database
D08555
Reactom Database
R-HSA-372519
R-HSA-9634834
CHEBI ID
CHEBI:45980
CHEBI:45978
CHEBI:9389
PubChem SID
26697094
Properties
No Data Available
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Molecule Details
A member of the class of acridines that is 1,2,3,4-tetrahydroacridine substituted by an amino group at position 9. It is used in the treatment of Alzheimer's disease.
Molecular Spectra
No Data Available
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References
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