Compile Data Set for Download or QSAR

Found 7 hits with Last Name = 'barrio' and Initial = 'jr'   

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 G/H synthase 2 (Mus musculus (Mouse))	BDBM50173287 (4-[3-(4-Fluoro-phenyl)-5-methyl-isoxazol-4-yl]-ben...) Show SMILES Cc1onc(c1-c1ccc(cc1)S(N)(=O)=O)-c1ccc(F)cc1 Show InChI InChI=1S/C16H13FN2O3S/c1-10-15(11-4-8-14(9-5-11)23(18,20)21)16(19-22-10)12-2-6-13(17)7-3-12/h2-9H,1H3,(H2,18,20,21)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
David Geffen School of Medicine at University of California Curated by ChEMBL					Assay Description Tested for prostaglandin E2 production as a function of COX-2 inhibition using endotoxin-treated murine RAW 264.7 macrophages				Bioorg Med Chem Lett 15: 4699-702 (2005) Article DOI: 10.1016/j.bmcl.2005.07.065 BindingDB Entry DOI: 10.7270/Q2H131KS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50173288 (4-(5-Fluoromethyl-3-phenyl-isoxazol-4-yl)-benzenes...) Show SMILES NS(=O)(=O)c1ccc(cc1)-c1c(CF)onc1-c1ccccc1 Show InChI InChI=1S/C16H13FN2O3S/c17-10-14-15(11-6-8-13(9-7-11)23(18,20)21)16(19-22-14)12-4-2-1-3-5-12/h1-9H,10H2,(H2,18,20,21)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
David Geffen School of Medicine at University of California Curated by ChEMBL					Assay Description Inhibitory activity against human recombinant cyclooxygenase 2				Bioorg Med Chem Lett 15: 4699-702 (2005) Article DOI: 10.1016/j.bmcl.2005.07.065 BindingDB Entry DOI: 10.7270/Q2H131KS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Mus musculus (Mouse))	BDBM50173288 (4-(5-Fluoromethyl-3-phenyl-isoxazol-4-yl)-benzenes...) Show SMILES NS(=O)(=O)c1ccc(cc1)-c1c(CF)onc1-c1ccccc1 Show InChI InChI=1S/C16H13FN2O3S/c17-10-14-15(11-6-8-13(9-7-11)23(18,20)21)16(19-22-14)12-4-2-1-3-5-12/h1-9H,10H2,(H2,18,20,21)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
David Geffen School of Medicine at University of California Curated by ChEMBL					Assay Description Tested for prostaglandin E2 production as a function of COX-2 inhibition using endotoxin-treated murine RAW 264.7 macrophages				Bioorg Med Chem Lett 15: 4699-702 (2005) Article DOI: 10.1016/j.bmcl.2005.07.065 BindingDB Entry DOI: 10.7270/Q2H131KS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Mus musculus (Mouse))	BDBM50173290 (4-[5-(2-Fluoro-ethyl)-3-phenyl-isoxazol-4-yl]-benz...) Show SMILES NS(=O)(=O)c1ccc(cc1)-c1c(CCF)onc1-c1ccccc1 Show InChI InChI=1S/C17H15FN2O3S/c18-11-10-15-16(12-6-8-14(9-7-12)24(19,21)22)17(20-23-15)13-4-2-1-3-5-13/h1-9H,10-11H2,(H2,19,21,22)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
David Geffen School of Medicine at University of California Curated by ChEMBL					Assay Description Tested for prostaglandin E2 production as a function of COX-2 inhibition using endotoxin-treated murine RAW 264.7 macrophages				Bioorg Med Chem Lett 15: 4699-702 (2005) Article DOI: 10.1016/j.bmcl.2005.07.065 BindingDB Entry DOI: 10.7270/Q2H131KS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Mus musculus (Mouse))	BDBM50173289 (2-Fluoro-4-(5-methyl-3-phenyl-isoxazol-4-yl)-benze...) Show SMILES Cc1onc(c1-c1ccc(c(F)c1)S(N)(=O)=O)-c1ccccc1 Show InChI InChI=1S/C16H13FN2O3S/c1-10-15(16(19-22-10)11-5-3-2-4-6-11)12-7-8-14(13(17)9-12)23(18,20)21/h2-9H,1H3,(H2,18,20,21)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
David Geffen School of Medicine at University of California Curated by ChEMBL					Assay Description Tested for prostaglandin E2 production as a function of COX-2 inhibition using endotoxin-treated murine RAW 264.7 macrophages				Bioorg Med Chem Lett 15: 4699-702 (2005) Article DOI: 10.1016/j.bmcl.2005.07.065 BindingDB Entry DOI: 10.7270/Q2H131KS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM13063 (4-(5-methyl-3-phenyl-1,2-oxazol-4-yl)benzene-1-sul...) Show SMILES Cc1onc(c1-c1ccc(cc1)S(N)(=O)=O)-c1ccccc1 Show InChI InChI=1S/C16H14N2O3S/c1-11-15(12-7-9-14(10-8-12)22(17,19)20)16(18-21-11)13-5-3-2-4-6-13/h2-10H,1H3,(H2,17,19,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
David Geffen School of Medicine at University of California Curated by ChEMBL					Assay Description Inhibitory activity against human recombinant cyclooxygenase 2				Bioorg Med Chem Lett 15: 4699-702 (2005) Article DOI: 10.1016/j.bmcl.2005.07.065 BindingDB Entry DOI: 10.7270/Q2H131KS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50173290 (4-[5-(2-Fluoro-ethyl)-3-phenyl-isoxazol-4-yl]-benz...) Show SMILES NS(=O)(=O)c1ccc(cc1)-c1c(CCF)onc1-c1ccccc1 Show InChI InChI=1S/C17H15FN2O3S/c18-11-10-15-16(12-6-8-14(9-7-12)24(19,21)22)17(20-23-15)13-4-2-1-3-5-13/h1-9H,10-11H2,(H2,19,21,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8	n/a	n/a	n/a	n/a	n/a	n/a
David Geffen School of Medicine at University of California Curated by ChEMBL					Assay Description Inhibitory activity against human recombinant cyclooxygenase 2				Bioorg Med Chem Lett 15: 4699-702 (2005) Article DOI: 10.1016/j.bmcl.2005.07.065 BindingDB Entry DOI: 10.7270/Q2H131KS
					More data for this Ligand-Target Pair