In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
October 24th, 2009 | 30 | No |
Popular Name: 1-[2-(cyclohexylamino)-5-nitro-phenyl]sulfonyl-3-heptyl-urea 1-[2-(cyclohexylamino)-5-nitro-p…
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) | 5.55 | 6.02 | -53.74 | 2 | 9 | -1 | 139 | 439.558 | 12 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
TA2R-1-E | Thromboxane A2 Receptor (cluster #1 Of 2), Eukaryotic | Eukaryotes | 3 | 0.40 | Binding ≤ 10μM |
TA2R-1-E | Thromboxane A2 Receptor (cluster #1 Of 1), Eukaryotic | Eukaryotes | 93 | 0.33 | Functional ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
TA2R_HUMAN | P21731 | Thromboxane A2 Receptor, Human | 2.5 | 0.40 | Binding ≤ 1μM |
TA2R_HUMAN | P21731 | Thromboxane A2 Receptor, Human | 2.5 | 0.40 | Binding ≤ 10μM |
TA2R_HUMAN | P21731 | Thromboxane A2 Receptor, Human | 55.55 | 0.34 | Functional ≤ 10μM |
Description | Species |
---|---|
G alpha (12/13) signalling events | |
G alpha (q) signalling events | |
Prostanoid ligand receptors | |
Thromboxane signalling through TP receptor |