[3H]prazosin
| SMILES | COc1cc2nc(nc(c2cc1OC)N)N1CCN(CC1)C(=O)c1ccco1 |
| InChIKey | IENZQIKPVFGBNW-UHFFFAOYSA-N |
Chemical properties
| Hydrogen bond acceptors | 8 |
| Hydrogen bond donors | 1 |
| Rotatable bonds | 4 |
| Molecular weight (Da) | 383.2 |
Drug properties
| Molecular type | Small molecule |
| Physiological/Surrogate | Surrogate |
| Approved drug | Yes |
Database connections
Bioactivities
| Receptor | Activity | Source | |||||||
|---|---|---|---|---|---|---|---|---|---|
| GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
| α1A | ADA1A | Human | Adrenoceptors | A | pKd | 9.1 | 9.1 | 9.1 | Guide to Pharmacology |
| α1B | ADA1B | Human | Adrenoceptors | A | pKd | 9.1 | 9.1 | 9.1 | Guide to Pharmacology |
| α1D | ADA1D | Human | Adrenoceptors | A | pKi | 8.7 | 8.7 | 8.7 | Guide to Pharmacology |
| α2A | ADA2A | Pig | Adrenoceptors | A | pKi | 5.39 | 5.39 | 5.39 | ChEMBL |
| α2A | ADA2A | Bovine | Adrenoceptors | A | pKi | 6.97 | 6.97 | 6.97 | ChEMBL |
| α1B | ADA1B | Golden hamster | Adrenoceptors | A | pKi | 9.08 | 9.08 | 9.08 | ChEMBL |
| α2A | ADA2A | Rat | Adrenoceptors | A | pKi | 5.78 | 5.78 | 5.78 | ChEMBL |
| α1A | ADA1A | Rabbit | Adrenoceptors | A | pKd | 8.3 | 8.3 | 8.3 | ChEMBL |
| α1A | ADA1A | Bovine | Adrenoceptors | A | pKi | 9.03 | 9.46 | 9.9 | ChEMBL |
| α1D | ADA1D | Rat | Adrenoceptors | A | pKi | 8.86 | 9.29 | 9.7 | ChEMBL |
| α1D | ADA1D | Rat | Adrenoceptors | A | pKd | 8.7 | 9.06 | 9.77 | ChEMBL |
| α1B | ADA1B | Rat | Adrenoceptors | A | pKd | 8.99 | 9.0 | 9.01 | ChEMBL |
| α1B | ADA1B | Rat | Adrenoceptors | A | pKi | 8.53 | 9.59 | 10.0 | ChEMBL |
| 5-HT1D | 5HT1D | Human | 5-Hydroxytryptamine | A | pKi | 9.48 | 9.48 | 9.48 | ChEMBL |
| α1B | ADA1B | Human | Adrenoceptors | A | pKi | 8.1 | 9.36 | 10.57 | ChEMBL |
| α1A | ADA1A | Rat | Adrenoceptors | A | pKd | 8.6 | 9.0 | 9.81 | ChEMBL |
| α1A | ADA1A | Rat | Adrenoceptors | A | pKi | 8.98 | 9.56 | 10.15 | ChEMBL |
| α1D | ADA1D | Human | Adrenoceptors | A | pKi | 9.34 | 9.55 | 9.77 | ChEMBL |
| α2B | ADA2B | Human | Adrenoceptors | A | pKi | 6.4 | 6.9 | 7.89 | ChEMBL |
| α2C | ADA2C | Human | Adrenoceptors | A | pKi | 6.21 | 6.97 | 7.62 | ChEMBL |
| 5-HT1A | 5HT1A | Rat | 5-Hydroxytryptamine | A | pKi | 5.63 | 5.63 | 5.63 | ChEMBL |
| D4 | DRD4 | Human | Dopamine | A | pKi | 5.08 | 5.08 | 5.08 | ChEMBL |
| α1A | ADA1A | Human | Adrenoceptors | A | pKi | 8.73 | 9.4 | 10.4 | ChEMBL |
| α2A | ADA2A | Human | Adrenoceptors | A | pKi | 5.67 | 6.12 | 6.68 | ChEMBL |
| 5-HT2B | 5HT2B | Human | 5-Hydroxytryptamine | A | pKi | 5.58 | 5.58 | 5.58 | ChEMBL |
| μ | OPRM | Human | Opioid | A | pKi | 5.75 | 5.75 | 5.75 | ChEMBL |
| 5-HT5A | 5HT5A | Human | 5-Hydroxytryptamine | A | pKi | 6.1 | 6.1 | 6.1 | ChEMBL |
| Receptor | Activity | Source | |||||||
|---|---|---|---|---|---|---|---|---|---|
| GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
| α1B | ADA1B | Rat | Adrenoceptors | A | pIC50 | 9.07 | 9.53 | 9.75 | ChEMBL |
| α1B | ADA1B | Human | Adrenoceptors | A | pIC50 | 8.06 | 8.06 | 8.06 | ChEMBL |
| α1A | ADA1A | Rat | Adrenoceptors | A | pIC50 | 9.16 | 9.47 | 9.66 | ChEMBL |
| M1 | ACM1 | Rat | Acetylcholine (muscarinic) | A | Potency | 4.55 | 4.7 | 4.85 | ChEMBL |
| α1D | ADA1D | Human | Adrenoceptors | A | pIC50 | 9.06 | 9.12 | 9.18 | ChEMBL |
| α2B | ADA2B | Human | Adrenoceptors | A | pIC50 | 6.54 | 6.54 | 6.54 | ChEMBL |
| α2C | ADA2C | Human | Adrenoceptors | A | pIC50 | 6.19 | 6.19 | 6.19 | ChEMBL |
| D2 | DRD2 | Rat | Dopamine | A | pIC50 | 4.96 | 4.96 | 4.96 | ChEMBL |
| α1A | ADA1A | Human | Adrenoceptors | A | pIC50 | 8.4 | 8.4 | 8.4 | ChEMBL |
| α2A | ADA2A | Human | Adrenoceptors | A | pIC50 | 5.58 | 5.58 | 5.58 | ChEMBL |
| 5-HT2B | 5HT2B | Human | 5-Hydroxytryptamine | A | pIC50 | 5.38 | 5.38 | 5.38 | ChEMBL |