In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
June 23rd, 2008 | 34 | No |
Popular Name: 2-[3-[2-(1,1-diphenylpropylsulfanyl)ethyl]-2-(hydroxymethyl)benzofuran-7-yl]oxyacetic 2-[3-[2-(1,1-diphenylpropylsulfa…
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) | 5.85 | 12.81 | -57.96 | 1 | 5 | -1 | 83 | 475.586 | 11 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
PI2R-1-E | Prostanoid IP Receptor (cluster #1 Of 2), Eukaryotic | Eukaryotes | 3400 | 0.23 | Binding ≤ 10μM |
TA2R-1-E | Thromboxane A2 Receptor (cluster #1 Of 2), Eukaryotic | Eukaryotes | 180 | 0.28 | Binding ≤ 10μM |
Z50587-1-O | Homo Sapiens (cluster #1 Of 9), Other | Other | 3800 | 0.22 | Functional ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
TA2R_HUMAN | P21731 | Thromboxane A2 Receptor, Human | 180 | 0.28 | Binding ≤ 1μM |
PI2R_HUMAN | P43119 | Prostanoid IP Receptor, Human | 3400 | 0.23 | Binding ≤ 10μM |
TA2R_HUMAN | P21731 | Thromboxane A2 Receptor, Human | 180 | 0.28 | Binding ≤ 10μM |
Z50587 | Z50587 | Homo Sapiens | 3800 | 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 |