In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
January 27th, 2010 | 29 | Yes |
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) | 1.60 | 9.88 | -50.64 | 0 | 6 | -1 | 92 | 494.412 | 5 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
PD2R-1-E | Prostanoid DP Receptor (cluster #1 Of 2), Eukaryotic | Eukaryotes | 3 | 0.41 | Binding ≤ 10μM |
TA2R-1-E | Thromboxane A2 Receptor (cluster #1 Of 2), Eukaryotic | Eukaryotes | 36 | 0.36 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
PD2R_HUMAN | Q13258 | Prostanoid DP Receptor, Human | 3.3 | 0.41 | Binding ≤ 1μM |
TA2R_HUMAN | P21731 | Thromboxane A2 Receptor, Human | 35.7 | 0.36 | Binding ≤ 1μM |
PD2R_HUMAN | Q13258 | Prostanoid DP Receptor, Human | 3.3 | 0.41 | Binding ≤ 10μM |
TA2R_HUMAN | P21731 | Thromboxane A2 Receptor, Human | 35.7 | 0.36 | Binding ≤ 10μM |
Description | Species |
---|---|
G alpha (12/13) signalling events | |
G alpha (q) signalling events | |
G alpha (s) signalling events | |
Prostanoid ligand receptors | |
Thromboxane signalling through TP receptor |