CHEMBL4469848
SMILES | FC(F)(F)c1cc(Oc2nccc3occc23)ccc1-c1cccc2nccn12 |
InChIKey | ZKXUDWLJTFYOAN-UHFFFAOYSA-N |
Chemical properties
Hydrogen bond acceptors | 5 |
Hydrogen bond donors | 0 |
Rotatable bonds | 3 |
Molecular weight (Da) | 395.1 |
Drug properties
Molecular type | Small molecule |
Endogenous/Surrogate | Surrogate |
Approved drug | No |
Database connections
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
5-HT1E | 5HT1E | Human | 5-Hydroxytryptamine | A | pKi | 5.0 | 5.0 | 5.0 | ChEMBL |
5-HT5A | 5HT5A | Human | 5-Hydroxytryptamine | A | pKi | 5.13 | 5.13 | 5.13 | ChEMBL |
D5 | DRD5 | Human | Dopamine | A | pKi | 7.33 | 7.33 | 7.33 | ChEMBL |
5-HT1B | 5HT1B | Human | 5-Hydroxytryptamine | A | pKi | 5.03 | 5.03 | 5.03 | ChEMBL |
5-HT1D | 5HT1D | Human | 5-Hydroxytryptamine | A | pKi | 5.05 | 5.05 | 5.05 | ChEMBL |
α1B | ADA1B | Human | Adrenoceptors | A | pKi | 5.13 | 5.13 | 5.13 | ChEMBL |
H2 | HRH2 | Human | Histamine | A | pKi | 5.17 | 5.17 | 5.17 | ChEMBL |
5-HT7 | 5HT7R | Human | 5-Hydroxytryptamine | A | pKi | 5.39 | 5.39 | 5.39 | ChEMBL |
β1 | ADRB1 | Human | Adrenoceptors | A | pKi | 5.07 | 5.07 | 5.07 | ChEMBL |
H1 | HRH1 | Human | Histamine | A | pKi | 5.01 | 5.01 | 5.01 | ChEMBL |
D4 | DRD4 | Human | Dopamine | A | pKi | 5.16 | 5.16 | 5.16 | ChEMBL |
α1A | ADA1A | Human | Adrenoceptors | A | pKi | 5.16 | 5.16 | 5.16 | ChEMBL |
α2A | ADA2A | Human | Adrenoceptors | A | pKi | 5.29 | 5.29 | 5.29 | ChEMBL |
D1 | DRD1 | Human | Dopamine | A | pKi | 6.82 | 6.82 | 6.82 | ChEMBL |
5-HT6 | 5HT6R | Human | 5-Hydroxytryptamine | A | pKi | 5.16 | 5.16 | 5.16 | ChEMBL |
5-HT2B | 5HT2B | Human | 5-Hydroxytryptamine | A | pKi | 6.08 | 6.08 | 6.08 | ChEMBL |
M2 | ACM2 | Human | Acetylcholine (muscarinic) | A | pKi | 5.09 | 5.09 | 5.09 | ChEMBL |
β2 | ADRB2 | Human | Adrenoceptors | A | pKi | 5.07 | 5.07 | 5.07 | ChEMBL |
M1 | ACM1 | Human | Acetylcholine (muscarinic) | A | pKi | 5.05 | 5.05 | 5.05 | ChEMBL |
5-HT2A | 5HT2A | Human | 5-Hydroxytryptamine | A | pKi | 5.37 | 5.37 | 5.37 | ChEMBL |
5-HT1A | 5HT1A | Human | 5-Hydroxytryptamine | A | pKi | 5.6 | 5.6 | 5.6 | ChEMBL |
κ | OPRK | Human | Opioid | A | pKi | 5.82 | 5.82 | 5.82 | ChEMBL |
μ | OPRM | Human | Opioid | A | pKi | 5.36 | 5.36 | 5.36 | ChEMBL |
D2 | DRD2 | Human | Dopamine | A | pKi | 5.12 | 5.12 | 5.12 | ChEMBL |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
D1 | DRD1 | Human | Dopamine | A | pEC50 | 6.57 | 7.61 | 8.64 | ChEMBL |