General Information
Drug ID
DR00183
Drug Name
Tacrine
Synonyms
1,2,3,4-TETRAHYDRO-9-ACRIDINAMINE; 1,2,3,4-TETRAHYDRO-9-ACRIDINAMINE (SEE ALSO 1684-40-8); 1,2,3,4-Tetrahydro-9-acridineamine; 1,2,3,4-Tetrahydro-acridin-9-ylamine; 1,2,3,4-Tetrahydroaminoacridine; 1,2,3,4-tetrahydroacridin-9-amine; 5-Amino-6,7,8,9-tetrahydroacridine (European); 9-AMINOTETRAHYDROACRIDINE; 9-Acridinamine, 1,2,3,4-tetrahydro-(9CI); 9-Amino-1,2,3,4-Tetrahydroacridine Hydrate Hydrochloride Hydrate; 9-amino-1,2,3,4-tetrahydroacridine; BBL001044; CS 12602; Cognex; Cognex (TN); Romotal; Tacrina; Tacrina [INN-Spanish]; Tacrinal; Tacrinal (TN); Tacrine (INN); Tacrine [INN:BAN]; Tacrine hydrochloride; Tacrinum; Tacrinum [INN-Latin]; Tenakrin; Tetrahydroaminacrine; Tetrahydroaminoacridine; Tetrahydroaminocrin; Tetrahydroaminocrine; Tha
Drug Type
Small molecular drug
Indication Alzheimer disease [ICD11:8A20] Approved [1]
Therapeutic Class
Parasympathomimetics
Structure
3D MOL 2D MOL
Formula
C13H14N2
Canonical SMILES
C1CCC2=NC3=CC=CC=C3C(=C2C1)N
InChI
InChI=1S/C13H14N2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1,3,5,7H,2,4,6,8H2,(H2,14,15)
InChIKey
YLJREFDVOIBQDA-UHFFFAOYSA-N
CAS Number
CAS 321-64-2
Pharmaceutical Properties Molecular Weight 198.26 Topological Polar Surface Area 38.9
Heavy Atom Count 15 Rotatable Bond Count 0
Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 2
XLogP
2.7
PubChem CID
1935
PubChem SID
10518487 ,10589113 ,11110734 ,11113824 ,11336111 ,11361350 ,11363310 ,11365872 ,11368434 ,11372617 ,11374476 ,11376596 ,11451154 ,11462322 ,11466357 ,11467477 ,11485559 ,11485994 ,11489628 ,11491524 ,11492634 ,11494230 ,15120928 ,24339135 ,26697094 ,26746578 ,26751997 ,26751998 ,29221124 ,3249865 ,4630 ,46392558 ,46393827 ,46393828 ,46505487 ,46509736 ,47291206 ,47365271 ,47440346 ,47440347 ,47515380 ,47515381 ,47589065 ,47736566 ,47736567 ,597209 ,7423820 ,7890757 ,7980766 ,8151345
ChEBI ID
ChEBI:45980
TTD Drug ID
D0E6YQ
DT(s) Transporting This Drug P-GP Transporter Info P-glycoprotein 1 Substrate [2]
References
1 Tacrine was approved by FDA. The official website of the U.S. Food and Drug Administration. (2019)
2 Tacrine sinusoidal uptake and biliary excretion in sandwich-cultured primary rat hepatocytes. J Pharm Pharm Sci. 2014;17(3):427-38.

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