| In ZINC since | Heavy atoms | Benign functionality |
|---|---|---|
| April 12th, 2010 | 22 | Yes |
Popular Name: (2S)-4-methyl-2-[[4-(morpholinomethyl)phenoxy]methyl]morpholine (2S)-4-methyl-2-[[4-(morpholinom…
| Type pH range | xlogP | Des A‑Pol Apolar desolvation (kcal/mol) | Des Pol Polar desolvation (kcal/mol) | H Don H-bond donors | H Acc H-bond acceptors | Chg Net charge | tPSA (Ų) | MWT Molecular weight (g/mol) | RB Rotatable bonds | DL |
|---|---|---|---|---|---|---|---|---|---|---|
| Ref Reference (pH 7) | 1.51 | 2.51 | -6.6 | 0 | 5 | 0 | 34 | 306.406 | 5 | ↓ |
| Mid Mid (pH 6-8) | 1.51 | 4.94 | -41.5 | 1 | 5 | 1 | 35 | 307.414 | 5 | ↓ |
| Lo Low (pH 4.5-6) | 1.51 | 7.2 | -84.35 | 2 | 5 | 2 | 37 | 308.422 | 5 | ↓ |
| Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
|---|---|---|---|---|---|
| HRH3-2-E | Histamine H3 Receptor (cluster #2 Of 3), Eukaryotic | Eukaryotes | 2100 | 0.36 | Binding ≤ 10μM |
| Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
|---|---|---|---|---|---|
| HRH3_HUMAN | Q9Y5N1 | Histamine H3 Receptor, Human | 2100 | 0.36 | Binding ≤ 10μM |
| Description | Species |
|---|---|
| G alpha (i) signalling events | |
| Histamine receptors |
