| In ZINC since | Heavy atoms | Benign functionality |
|---|---|---|
| February 21st, 2009 | 49 | No |
| 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) | 4.70 | 16.67 | -61.46 | 0 | 10 | -1 | 121 | 693.253 | 11 | ↓ |
| Mid Mid (pH 6-8) | 4.70 | 17.54 | -70.59 | 1 | 10 | 0 | 123 | 694.261 | 11 | ↓ |
| Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
|---|---|---|---|---|---|
| PTAFR-1-E | Platelet Activating Factor Receptor (cluster #1 Of 3), Eukaryotic | Eukaryotes | 980 | 0.17 | Functional ≤ 10μM |
| THAS-1-E | Thromboxane-A Synthase (cluster #1 Of 1), Eukaryotic | Eukaryotes | 24 | 0.22 | Functional ≤ 10μM |
| Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
|---|---|---|---|---|---|
| PTAFR_MOUSE | Q62035 | Platelet Activating Factor Receptor, Mouse | 980 | 0.17 | Functional ≤ 10μM |
| PTAFR_RAT | P46002 | Platelet Activating Factor Receptor, Rat | 980 | 0.17 | Functional ≤ 10μM |
| PTAFR_HUMAN | P25105 | Platelet Activating Factor Receptor, Human | 980 | 0.17 | Functional ≤ 10μM |
| THAS_HUMAN | P24557 | Thromboxane-A Synthase, Human | 24 | 0.22 | Functional ≤ 10μM |
| Description | Species |
|---|---|
| Class A/1 (Rhodopsin-like receptors) | |
| Eicosanoids | |
| G alpha (q) signalling events | |
| Interferon gamma signaling | |
| Synthesis of Prostaglandins (PG) and Thromboxanes (TX) |
