In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
November 16th, 2010 | 38 | Yes |
Popular Name: MORPHICEPTIN MORPHICEPTIN
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) | 0.17 | 4.37 | -22.61 | 6 | 10 | 0 | 159 | 521.618 | 9 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
OPRM-1-E | Mu-type Opioid Receptor (cluster #1 Of 4), Eukaryotic | Eukaryotes | 35 | 0.27 | Binding ≤ 10μM |
OPRM-1-E | Mu-type Opioid Receptor (cluster #1 Of 4), Eukaryotic | Eukaryotes | 320 | 0.24 | Binding ≤ 10μM |
Z50512-1-O | Cavia Porcellus (cluster #1 Of 7), Other | Other | 109 | 0.26 | Functional ≤ 10μM |
Z50594-4-O | Mus Musculus (cluster #4 Of 9), Other | Other | 594 | 0.23 | Functional ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
OPRM_HUMAN | P35372 | Mu Opioid Receptor, Human | 150 | 0.25 | Binding ≤ 1μM |
OPRM_RAT | P33535 | Mu Opioid Receptor, Rat | 35.2 | 0.27 | Binding ≤ 1μM |
OPRM_RAT | P33535 | Mu Opioid Receptor, Rat | 35.2 | 0.27 | Binding ≤ 10μM |
OPRM_HUMAN | P35372 | Mu Opioid Receptor, Human | 150 | 0.25 | Binding ≤ 10μM |
Z50512 | Z50512 | Cavia Porcellus | 109 | 0.26 | Functional ≤ 10μM |
Z50594 | Z50594 | Mus Musculus | 594 | 0.23 | Functional ≤ 10μM |
Description | Species |
---|---|
G alpha (i) signalling events | |
G-protein activation | |
Opioid Signalling | |
Peptide ligand-binding receptors |
No pre-computed analogs available. Try a structural similarity search.