Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Lysophosphatidic acid receptor 2' and Ligand = 'BDBM50148351'   

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
Lysophosphatidic acid receptor 2 (Homo sapiens (Human))	BDBM50148351 (CHEMBL117529 | [3-((Z)-Octadec-9-enoylamino)-propi...) Show SMILES CCCCCCCC\C=C/CCCCCCCC(=O)NCCC(=O)P(O)(O)=O Show InChI InChI=1S/C21H40NO5P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20(23)22-19-18-21(24)28(25,26)27/h9-10H,2-8,11-19H2,1H3,(H,22,23)(H2,25,26,27)/b10-9-	NCI pathway Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	1.09E+3	n/a	n/a	n/a	n/a
Universidad Complutense de Madrid Curated by ChEMBL					Assay Description Agonist activity at LPA2 (unknown origin) by [35S]GTPgammaS binding assay				J Med Chem 63: 2372-2390 (2020) Article DOI: 10.1021/acs.jmedchem.9b01287 BindingDB Entry DOI: 10.7270/Q2DF6VSR
					More data for this Ligand-Target Pair
Lysophosphatidic acid receptor 2 (Homo sapiens (Human))	BDBM50148351 (CHEMBL117529 | [3-((Z)-Octadec-9-enoylamino)-propi...) Show SMILES CCCCCCCC\C=C/CCCCCCCC(=O)NCCC(=O)P(O)(O)=O Show InChI InChI=1S/C21H40NO5P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20(23)22-19-18-21(24)28(25,26)27/h9-10H,2-8,11-19H2,1H3,(H,22,23)(H2,25,26,27)/b10-9-	NCI pathway Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	1.09E+3	n/a	n/a	n/a	n/a
Oxford University Curated by ChEMBL					Assay Description Agonistic activity against lysophosphatidic acid receptor 2 using [35S]-GTP-gammaS as radioligand tested in vitro				Bioorg Med Chem Lett 14: 3473-6 (2004) Article DOI: 10.1016/j.bmcl.2004.04.061 BindingDB Entry DOI: 10.7270/Q2D50MDW
					More data for this Ligand-Target Pair