p-F-HHSiD


SMILES Fc1ccc(cc1)[Si](C1CCCCC1)(CCCN1CCCCC1)O
InChIKey ZNSZQJHTFRQUPD-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 2
Hydrogen bond donors 1
Rotatable bonds 6
Molecular weight (Da) 349.2

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug No

Database connections

Ligand site mutations M1

Sankey plot

Compound is not listed as a drug.

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
M1 ACM1 Human Acetylcholine (muscarinic) A pKi 7.1 7.45 7.8 Guide to Pharmacology
M2 ACM2 Human Acetylcholine (muscarinic) A pKi 6.1 6.35 6.6 Guide to Pharmacology
M3 ACM3 Human Acetylcholine (muscarinic) A pKi 7.3 7.6 7.9 Guide to Pharmacology
M4 ACM4 Human Acetylcholine (muscarinic) A pKi 7.1 7.3 7.5 Guide to Pharmacology
M5 ACM5 Human Acetylcholine (muscarinic) A pKi 6.3 6.3 6.3 Guide to Pharmacology
M1 ACM1 Human Acetylcholine (muscarinic) A pKi 7.32 7.32 7.32 PDSP Ki database
M2 ACM2 Rat Acetylcholine (muscarinic) A pKi 6.52 6.64 6.76 PDSP Ki database
M3 ACM3 Rat Acetylcholine (muscarinic) A pKi 7.3 7.3 7.3 PDSP Ki database
M2 ACM2 Human Acetylcholine (muscarinic) A pKi 6.82 6.82 6.82 PDSP Ki database
M4 ACM4 Rat Acetylcholine (muscarinic) A pKi 6.96 7.0 7.03 PDSP Ki database
M4 ACM4 Mouse Acetylcholine (muscarinic) A pKi 7.0 7.0 7.0 PDSP Ki database
M3 ACM3 Rat Acetylcholine (muscarinic) A pKi 8.0 8.0 8.0 Guide to Pharmacology
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
NPS NPSR1 Human Neuropeptide S A Potency 4.9 4.9 4.9 ChEMBL