Compile Data Set for Download or QSAR

Found 2 hits of ki for monomerid = 50331731   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Prostaglandin D2 receptor (Homo sapiens (Human))	BDBM50331731 (2-((R)-9-((S)-1-(4-chlorophenyl)ethyl)-6-fluoro-8-...) Show SMILES C[C@@H](c1ccc(Cl)cc1)n1c2[C@@H](CC(O)=O)CCCc2c2cc(F)cc(c12)S(C)(=O)=O |r| Show InChI InChI=1S/C23H23ClFNO4S/c1-13(14-6-8-16(24)9-7-14)26-22-15(10-21(27)28)4-3-5-18(22)19-11-17(25)12-20(23(19)26)31(2,29)30/h6-9,11-13,15H,3-5,10H2,1-2H3,(H,27,28)/t13-,15+/m0/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	0.75	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Merck Frosst Centre for Therapeutic Research Curated by ChEMBL					Assay Description Antagonist activity at prostanoid DP1 receptor				Bioorg Med Chem Lett 20: 7462-5 (2010) Article DOI: 10.1016/j.bmcl.2010.10.018 BindingDB Entry DOI: 10.7270/Q2PZ5920
					More data for this Ligand-Target Pair
Thromboxane A2 receptor (Homo sapiens (Human))	BDBM50331731 (2-((R)-9-((S)-1-(4-chlorophenyl)ethyl)-6-fluoro-8-...) Show SMILES C[C@@H](c1ccc(Cl)cc1)n1c2[C@@H](CC(O)=O)CCCc2c2cc(F)cc(c12)S(C)(=O)=O |r| Show InChI InChI=1S/C23H23ClFNO4S/c1-13(14-6-8-16(24)9-7-14)26-22-15(10-21(27)28)4-3-5-18(22)19-11-17(25)12-20(23(19)26)31(2,29)30/h6-9,11-13,15H,3-5,10H2,1-2H3,(H,27,28)/t13-,15+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	184	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Merck Frosst Centre for Therapeutic Research Curated by ChEMBL					Assay Description Antagonist activity at prostanoid TP receptor				Bioorg Med Chem Lett 20: 7462-5 (2010) Article DOI: 10.1016/j.bmcl.2010.10.018 BindingDB Entry DOI: 10.7270/Q2PZ5920
					More data for this Ligand-Target Pair