IFENPRODIL
SMILES | CC(C(O)c1ccc(O)cc1)N1CCC(Cc2ccccc2)CC1 |
InChIKey | UYNVMODNBIQBMV-UHFFFAOYSA-N |
Chemical properties
Hydrogen bond acceptors | 3 |
Hydrogen bond donors | 2 |
Rotatable bonds | 5 |
Molecular weight (Da) | 325.2 |
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 |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
5-HT2A | 5HT2A | Bovine | 5-Hydroxytryptamine | A | pIC50 | 6.21 | 6.21 | 6.21 | ChEMBL |
5-HT1A | 5HT1A | Mouse | 5-Hydroxytryptamine | A | pIC50 | 6.62 | 6.62 | 6.62 | ChEMBL |
H1 | HRH1 | Human | Histamine | A | pIC50 | 6.0 | 6.0 | 6.0 | ChEMBL |
NPS | NPSR1 | Human | Neuropeptide S | A | Potency | 5.4 | 5.4 | 5.4 | ChEMBL |
H1 | HRH1 | Human | Histamine | A | pIC50 | 8.22 | 8.22 | 8.22 | Drug Central |
5-HT2A | 5HT2A | Bovine | 5-Hydroxytryptamine | A | pIC50 | 8.21 | 8.21 | 8.21 | Drug Central |
5-HT1A | 5HT1A | Mouse | 5-Hydroxytryptamine | A | pIC50 | 8.18 | 8.18 | 8.18 | Drug Central |
α2A | ADA2A | Rat | Adrenoceptors | A | pIC50 | 8.16 | 8.16 | 8.16 | Drug Central |