propantheline


SMILES O=C(C1c2ccccc2Oc2c1cccc2)OCC[N+](C(C)C)(C(C)C)C
InChIKey VVWYOYDLCMFIEM-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 3
Hydrogen bond donors 0
Rotatable bonds 6
Molecular weight (Da) 368.2

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
M1 ACM1 Human Acetylcholine (muscarinic) A pKi 8.01 8.01 8.01 Drug Central
M1 ACM1 Human Acetylcholine (muscarinic) A pKi 9.7 9.7 9.7 Guide to Pharmacology
M2 ACM2 Human Acetylcholine (muscarinic) A pKi 8.02 8.02 8.02 Drug Central
M2 ACM2 Human Acetylcholine (muscarinic) A pKi 9.5 9.5 9.5 Guide to Pharmacology
M3 ACM3 Human Acetylcholine (muscarinic) A pKi 8.0 8.0 8.0 Drug Central
M3 ACM3 Human Acetylcholine (muscarinic) A pKi 10.0 10.0 10.0 Guide to Pharmacology
M4 ACM4 Human Acetylcholine (muscarinic) A pKi 7.99 7.99 7.99 Drug Central
M4 ACM4 Human Acetylcholine (muscarinic) A pKi 10.2 10.2 10.2 Guide to Pharmacology
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
TSH TSHR Human Glycoprotein hormone A Potency 5.1 5.1 5.1 ChEMBL
M1 ACM1 Rat Acetylcholine (muscarinic) A Potency 7.95 8.47 9.0 ChEMBL