N-methylhistamine
| SMILES | Cn1cc(nc1)CCN |
| InChIKey | FHQDWPCFSJMNCT-UHFFFAOYSA-N |
Chemical properties
| Hydrogen bond acceptors | 3 |
| Hydrogen bond donors | 1 |
| Rotatable bonds | 2 |
| Molecular weight (Da) | 125.1 |
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 |
| H3 | HRH3 | Human | Histamine | A | pKi | 8.6 | 8.95 | 9.3 | Guide to Pharmacology |
| H4 | HRH4 | Human | Histamine | A | pKi | 7.3 | 7.45 | 7.6 | Guide to Pharmacology |
| H4 | HRH4 | Mouse | Histamine | A | pKi | 6.5 | 6.5 | 6.5 | Guide to Pharmacology |
| H4 | HRH4 | Rat | Histamine | A | pKi | 6.3 | 6.3 | 6.3 | Guide to Pharmacology |
| H3 | HRH3 | Rat | Histamine | A | pKi | 8.8 | 8.8 | 8.8 | Guide to Pharmacology |
| Receptor | Activity | Source | |||||||
|---|---|---|---|---|---|---|---|---|---|
| GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |