ACECLIDINE


SMILES CC(=O)OC1CN2CCC1CC2
InChIKey WRJPSSPFHGNBMG-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 3
Hydrogen bond donors 0
Rotatable bonds 1
Molecular weight (Da) 169.1

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug No

Database connections


Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
M2 ACM2 Human Acetylcholine (muscarinic) A pKi 5.65 5.93 6.21 PDSP Ki database
M4 ACM4 Human Acetylcholine (muscarinic) A pKi 5.0 5.19 5.38 PDSP Ki database
M2 ACM2 Rat Acetylcholine (muscarinic) A pKi 5.0 5.18 5.36 PDSP Ki database
M3 ACM3 Rat Acetylcholine (muscarinic) A pKi 5.0 6.33 7.65 PDSP Ki database
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
M3 ACM3 Mouse Acetylcholine (muscarinic) A pEC50 5.0 5.0 5.0 ChEMBL
M1 ACM1 Rat Acetylcholine (muscarinic) A pIC50 5.62 6.27 6.92 ChEMBL
M1 ACM1 Human Acetylcholine (muscarinic) A pEC50 5.35 5.35 5.35 ChEMBL
M2 ACM2 Human Acetylcholine (muscarinic) A pEC50 8.24 8.24 8.24 Drug Central
M1 ACM1 Human Acetylcholine (muscarinic) A pEC50 8.3 8.3 8.3 Drug Central
M3 ACM3 Human Acetylcholine (muscarinic) A pEC50 8.29 8.29 8.29 Drug Central
M4 ACM4 Human Acetylcholine (muscarinic) A pEC50 8.32 8.32 8.32 Drug Central
M5 ACM5 Human Acetylcholine (muscarinic) A pEC50 8.29 8.29 8.29 Drug Central
M1 ACM1 Rat Acetylcholine (muscarinic) A pIC50 8.16 8.16 8.16 Drug Central