In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
July 29th, 2010 | 26 | Yes |
Popular Name: N-(9,10-dihydroanthracen-9-ylmethyl)-4-phenyl-butan-1-amine N-(9,10-dihydroanthracen-9-ylmet…
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) | 5.63 | 14.9 | -41.62 | 2 | 1 | 1 | 17 | 342.506 | 7 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
5HT2A-1-E | Serotonin 2a (5-HT2a) Receptor (cluster #1 Of 3), Eukaryotic | Eukaryotes | 365 | 0.35 | Binding ≤ 10μM |
HRH1-2-E | Histamine H1 Receptor (cluster #2 Of 2), Eukaryotic | Eukaryotes | 964 | 0.32 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
HRH1_HUMAN | P35367 | Histamine H1 Receptor, Human | 964 | 0.32 | Binding ≤ 1μM |
5HT2A_HUMAN | P28223 | Serotonin 2a (5-HT2a) Receptor, Human | 365 | 0.35 | Binding ≤ 1μM |
HRH1_HUMAN | P35367 | Histamine H1 Receptor, Human | 964 | 0.32 | Binding ≤ 10μM |
5HT2A_HUMAN | P28223 | Serotonin 2a (5-HT2a) Receptor, Human | 365 | 0.35 | Binding ≤ 10μM |
Description | Species |
---|---|
G alpha (q) signalling events | |
Histamine receptors | |
Serotonin receptors |