DIHYDREXIDINE
SMILES | Oc1cc2c(cc1O)[C@H]1c3ccccc3CN[C@@H]1CC2 |
InChIKey | BGOQGUHWXBGXJW-RHSMWYFYSA-N |
Chemical properties
Hydrogen bond acceptors | 3 |
Hydrogen bond donors | 3 |
Rotatable bonds | 0 |
Molecular weight (Da) | 267.1 |
Drug properties
Molecular type | Small molecule |
Physiological/Surrogate | Surrogate |
Approved drug | No |
Database connections
Ligand site mutations | D2 |
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
D5 | DRD5 | Rat | Dopamine | A | pKi | 7.8 | 7.8 | 7.8 | ChEMBL |
D4 | DRD4 | Rat | Dopamine | A | pKi | 7.89 | 7.89 | 7.89 | ChEMBL |
D1 | DRD1 | Pig | Dopamine | A | pKi | 7.68 | 7.68 | 7.68 | ChEMBL |
D3 | DRD3 | Rat | Dopamine | A | pKi | 6.77 | 6.77 | 6.77 | ChEMBL |
5-HT2C | 5HT2C | Rat | 5-Hydroxytryptamine | A | pKi | 5.62 | 5.62 | 5.62 | ChEMBL |
D1 | DRD1 | Rat | Dopamine | A | pKi | 7.0 | 7.0 | 7.0 | ChEMBL |
β1 | ADRB1 | Human | Adrenoceptors | A | pKi | 5.82 | 5.82 | 5.82 | ChEMBL |
D1 | DRD1 | Human | Dopamine | A | pKi | 5.92 | 7.31 | 8.21 | ChEMBL |
D2 | DRD2 | Rat | Dopamine | A | pKd | 4.89 | 5.4 | 5.64 | ChEMBL |
D2 | DRD2 | Rat | Dopamine | A | pKi | 5.85 | 5.85 | 5.85 | ChEMBL |
β2 | ADRB2 | Human | Adrenoceptors | A | pKi | 5.92 | 5.92 | 5.92 | ChEMBL |
D2 | DRD2 | Human | Dopamine | A | pKi | 5.58 | 6.14 | 7.24 | ChEMBL |
β2 | ADRB2 | Rat | Adrenoceptors | A | pKi | 5.0 | 5.0 | 5.0 | PDSP Ki database |
D1 | DRD1 | Human | Dopamine | A | pKi | 7.45 | 7.54 | 7.68 | PDSP Ki database |
D2 | DRD2 | Human | Dopamine | A | pKi | 5.58 | 6.01 | 6.62 | PDSP Ki database |
D1 | DRD1 | Rat | Dopamine | A | pKi | 8.0 | 8.2 | 8.64 | PDSP Ki database |
D1 | DRD1 | Rhesus macaque | Dopamine | A | pKi | 7.69 | 7.69 | 7.69 | PDSP Ki database |
D2 | DRD2 | Rat | Dopamine | A | pKi | 5.83 | 7.01 | 7.85 | PDSP Ki database |
D3 | DRD3 | Rat | Dopamine | A | pKi | 6.77 | 7.25 | 7.74 | PDSP Ki database |
D5 | DRD5 | Rat | Dopamine | A | pKi | 7.8 | 7.8 | 7.8 | PDSP Ki database |
D4 | DRD4 | Rat | Dopamine | A | pKi | 7.89 | 7.89 | 7.89 | PDSP Ki database |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
D1 | DRD1 | Goldfish | Dopamine | A | pEC50 | 7.06 | 7.06 | 7.06 | ChEMBL |
D1 | DRD1 | Rat | Dopamine | A | pIC50 | 6.83 | 7.82 | 8.25 | ChEMBL |
D1 | DRD1 | Rat | Dopamine | A | pEC50 | 7.52 | 7.52 | 7.52 | ChEMBL |
D1 | DRD1 | Human | Dopamine | A | pEC50 | 7.72 | 7.89 | 8.14 | ChEMBL |
D2 | DRD2 | Rat | Dopamine | A | pIC50 | 5.9 | 6.75 | 7.06 | ChEMBL |
D2 | DRD2 | Rat | Dopamine | A | pEC50 | 7.16 | 7.16 | 7.16 | ChEMBL |
D4 | DRD4 | Human | Dopamine | A | pEC50 | 7.77 | 7.77 | 7.77 | ChEMBL |
D2 | DRD2 | Human | Dopamine | A | pEC50 | 5.79 | 5.79 | 5.79 | ChEMBL |
TSH | TSHR | Human | Glycoprotein hormone | A | Potency | 5.3 | 5.3 | 5.3 | ChEMBL |