aclidinium


SMILES O=C(C(c1cccs1)(c1cccs1)O)O[C@H]1C[N+]2(CCCOc3ccccc3)CCC1CC2
InChIKey ASMXXROZKSBQIH-VITNCHFBSA-N

Chemical properties

Hydrogen bond acceptors 6
Hydrogen bond donors 1
Rotatable bonds 9
Molecular weight (Da) 484.2

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug Yes

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
M3 ACM3 Human Acetylcholine (muscarinic) A pKi 10.1 10.15 10.2 Guide to Pharmacology
M4 ACM4 Human Acetylcholine (muscarinic) A pKi 10.0 10.0 10.0 Guide to Pharmacology
M5 ACM5 Human Acetylcholine (muscarinic) A pKi 9.9 9.9 9.9 Guide to Pharmacology
M3 ACM3 Human Acetylcholine (muscarinic) A pKi 9.25 9.7 10.15 ChEMBL
M2 ACM2 Human Acetylcholine (muscarinic) A pKi 9.37 9.73 10.1 ChEMBL
M2 ACM2 Human Acetylcholine (muscarinic) A pKi 8.0 8.0 8.0 Drug Central
M3 ACM3 Human Acetylcholine (muscarinic) A pKi 7.99 7.99 7.99 Drug Central
M1 ACM1 Human Acetylcholine (muscarinic) A pKi 8.0 8.0 8.0 Drug Central
M1 ACM1 Human Acetylcholine (muscarinic) A pKi 10.1 10.1 10.1 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
M1 ACM1 Human Acetylcholine (muscarinic) A pIC50 10.1 10.15 10.2 Guide to Pharmacology
M2 ACM2 Human Acetylcholine (muscarinic) A pIC50 10.1 10.1 10.1 Guide to Pharmacology
M5 ACM5 Human Acetylcholine (muscarinic) A pIC50 9.8 9.8 9.8 ChEMBL
M4 ACM4 Human Acetylcholine (muscarinic) A pIC50 9.7 9.7 9.7 ChEMBL
M3 ACM3 Human Acetylcholine (muscarinic) A pIC50 8.36 9.34 9.9 ChEMBL
M2 ACM2 Human Acetylcholine (muscarinic) A pIC50 9.77 9.84 9.9 ChEMBL
M5 ACM5 Human Acetylcholine (muscarinic) A pIC50 8.01 8.01 8.01 Drug Central
M1 ACM1 Human Acetylcholine (muscarinic) A pIC50 9.85 9.93 10.0 ChEMBL
M4 ACM4 Human Acetylcholine (muscarinic) A pIC50 8.01 8.01 8.01 Drug Central