In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
September 26th, 2005 | 33 | Yes |
None
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) | 3.45 | 8.84 | -19.74 | 2 | 6 | 0 | 78 | 438.462 | 3 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
CCKAR-1-E | Cholecystokinin A Receptor (cluster #1 Of 1), Eukaryotic | Eukaryotes | 1 | 0.38 | Binding ≤ 10μM |
GASR-1-E | Cholecystokinin B Receptor (cluster #1 Of 1), Eukaryotic | Eukaryotes | 310 | 0.28 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
CCKAR_RAT | P30551 | Cholecystokinin A Receptor, Rat | 0.67 | 0.39 | Binding ≤ 1μM |
GASR_HUMAN | P32239 | Cholecystokinin B Receptor, Human | 310 | 0.28 | Binding ≤ 1μM |
CCKAR_RAT | P30551 | Cholecystokinin A Receptor, Rat | 0.67 | 0.39 | Binding ≤ 10μM |
GASR_HUMAN | P32239 | Cholecystokinin B Receptor, Human | 310 | 0.28 | Binding ≤ 10μM |
Description | Species |
---|---|
G alpha (q) signalling events | |
Gastrin-CREB signalling pathway via PKC and MAPK | |
Peptide ligand-binding receptors |