| In ZINC since | Heavy atoms | Benign functionality |
|---|---|---|
| June 23rd, 2008 | 35 | No |
Popular Name: 2-[3-[2-(1,1-diphenylethylsulfanyl)ethyl]-2-(3-hydroxypropyl)benzofuran-7-yl]oxyacetic 2-[3-[2-(1,1-diphenylethylsulfan…
| 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) | 5.83 | 13.92 | -57.28 | 1 | 5 | -1 | 83 | 489.613 | 12 | ↓ |
| Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
|---|---|---|---|---|---|
| PI2R-1-E | Prostanoid IP Receptor (cluster #1 Of 2), Eukaryotic | Eukaryotes | 5800 | 0.21 | Binding ≤ 10μM |
| TA2R-1-E | Thromboxane A2 Receptor (cluster #1 Of 2), Eukaryotic | Eukaryotes | 72 | 0.29 | Binding ≤ 10μM |
| Z50587-1-O | Homo Sapiens (cluster #1 Of 9), Other | Other | 9000 | 0.20 | Functional ≤ 10μM |
| Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
|---|---|---|---|---|---|
| TA2R_HUMAN | P21731 | Thromboxane A2 Receptor, Human | 72 | 0.29 | Binding ≤ 1μM |
| PI2R_HUMAN | P43119 | Prostanoid IP Receptor, Human | 5800 | 0.21 | Binding ≤ 10μM |
| TA2R_HUMAN | P21731 | Thromboxane A2 Receptor, Human | 72 | 0.29 | Binding ≤ 10μM |
| Z50587 | Z50587 | Homo Sapiens | 2900 | 0.22 | Functional ≤ 10μM |
| Description | Species |
|---|---|
| G alpha (12/13) signalling events | |
| G alpha (q) signalling events | |
| G alpha (s) signalling events | |
| Prostacyclin signalling through prostacyclin receptor | |
| Prostanoid ligand receptors | |
| Thromboxane signalling through TP receptor |