In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
August 11th, 2009 | 28 | Yes |
Popular Name: (2R)-2-methoxy-N-[(3R,4S)-3-methyl-1-phenethyl-4-piperidyl]-N-phenyl-propanamide (2R)-2-methoxy-N-[(3R,4S)-3-meth…
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) | 4.41 | 12.8 | -43.66 | 1 | 4 | 1 | 34 | 381.54 | 7 | ↓ |
Hi High (pH 8-9.5) | 4.41 | 10.56 | -8.08 | 0 | 4 | 0 | 33 | 380.532 | 7 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
OPRM-1-E | Mu-type Opioid Receptor (cluster #1 Of 4), Eukaryotic | Eukaryotes | 4 | 0.42 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
OPRM_RAT | P33535 | Mu Opioid Receptor, Rat | 32.2 | 0.37 | Binding ≤ 1μM |
OPRM_RAT | P33535 | Mu Opioid Receptor, Rat | 32.2 | 0.37 | Binding ≤ 10μM |
Description | Species |
---|---|
G alpha (i) signalling events | |
G-protein activation | |
Opioid Signalling | |
Peptide ligand-binding receptors |