tacrine


SMILES Nc1c2CCCCc2nc2c1cccc2
InChIKey YLJREFDVOIBQDA-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 2
Hydrogen bond donors 1
Rotatable bonds 0
Molecular weight (Da) 198.1

Drug properties

Molecular type Small molecule
Endogenous/Surrogate Surrogate
Approved drug Yes

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
M2 ACM2 Mouse Acetylcholine (muscarinic) A pKi 6.66 6.66 6.66 ChEMBL
M2 ACM2 Human Acetylcholine (muscarinic) A pKi 5.24 5.24 5.24 ChEMBL
CB1 CNR1 Human Cannabinoid A pKi 6.0 6.0 6.0 PDSP Ki database
α1D ADA1D Human Adrenoceptors A pKi 8.23 8.23 8.23 Drug Central
CB2 CNR2 Human Cannabinoid A pKi 6.0 6.0 6.0 PDSP Ki database
M2 ACM2 Mouse Acetylcholine (muscarinic) A pKi 8.18 8.18 8.18 Drug Central
α1A ADA1A Rat Adrenoceptors A pKi 5.95 5.95 5.95 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
M2 ACM2 Mouse Acetylcholine (muscarinic) A pIC50 5.68 5.68 5.68 ChEMBL
M2 ACM2 Pig Acetylcholine (muscarinic) A pEC50 5.2 5.2 5.2 ChEMBL
M2 ACM2 Rat Acetylcholine (muscarinic) A pIC50 5.68 5.68 5.68 ChEMBL
TSH TSHR Human Glycoprotein hormone A Potency 4.4 4.63 4.9 ChEMBL
M1 ACM1 Human Acetylcholine (muscarinic) A pIC50 4.89 4.89 4.89 ChEMBL
M1 ACM1 Mouse Acetylcholine (muscarinic) A pIC50 8.24 8.24 8.24 Drug Central
M1 ACM1 Mouse Acetylcholine (muscarinic) A pIC50 5.7 5.7 5.7 ChEMBL
M1 ACM1 Mouse Acetylcholine (muscarinic) A pIC50 5.7 5.7 5.7 Guide to Pharmacology
M2 ACM2 Mouse Acetylcholine (muscarinic) A pIC50 5.68 5.68 5.68 Guide to Pharmacology
M2 ACM2 Rat Acetylcholine (muscarinic) A pIC50 8.25 8.25 8.25 Drug Central
α1A ADA1A Rat Adrenoceptors A pIC50 8.25 8.25 8.25 Drug Central
α1A ADA1A Rat Adrenoceptors A pIC50 5.56 5.56 5.56 ChEMBL
M2 ACM2 Pig Acetylcholine (muscarinic) A pEC50 8.28 8.28 8.28 Drug Central
M1 ACM1 Rat Acetylcholine (muscarinic) A Potency 4.75 4.88 5.0 ChEMBL