BDBM50140707 5-(3-chloro-4-methylphenyl)-3-phenyl-(3R,3aS,6aR)-spiro[perhydrofuro[3,4-c]pyrrole-1,2''-(2'',3''-dihydro-1''H-indene)]-1'',3'',4,6-tetraone::CHEMBL26946::CHEMBL281883

SMILES: Cc1ccc(cc1Cl)-n1c(O)c2C(OC3(C(=O)c4ccccc4C3=O)c2c1O)c1ccccc1

InChI Key: InChIKey=WZLJTSSHRBYEDZ-UHFFFAOYSA-N

Data: 6 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 50140707   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Phenylalanyl-tRNA synthetase alpha chain (Streptococcus pyogenes serotype M18)	BDBM50140707 (5-(3-chloro-4-methylphenyl)-3-phenyl-(3R,3aS,6aR)-...) Show SMILES Cc1ccc(cc1Cl)-n1c(O)c2C(OC3(C(=O)c4ccccc4C3=O)c2c1O)c1ccccc1 Show InChI InChI=1S/C27H18ClNO5/c1-14-11-12-16(13-19(14)28)29-25(32)20-21(26(29)33)27(34-22(20)15-7-3-2-4-8-15)23(30)17-9-5-6-10-18(17)24(27)31/h2-13,22,32-33H,1H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	220	n/a	n/a	n/a	n/a	n/a	n/a
Cubist Pharmaceuticals Inc. Curated by ChEMBL					Assay Description Inhibitory activity against phenylalanyl-tRNA synthetase from Enterococcus faecalis				Bioorg Med Chem Lett 14: 1339-42 (2004) Article DOI: 10.1016/j.bmcl.2003.11.081 BindingDB Entry DOI: 10.7270/Q2PR7VDS
					More data for this Ligand-Target Pair
Phenylalanyl-tRNA synthetase mitochondrial (Homo sapiens (Human))	BDBM50140707 (5-(3-chloro-4-methylphenyl)-3-phenyl-(3R,3aS,6aR)-...) Show SMILES Cc1ccc(cc1Cl)-n1c(O)c2C(OC3(C(=O)c4ccccc4C3=O)c2c1O)c1ccccc1 Show InChI InChI=1S/C27H18ClNO5/c1-14-11-12-16(13-19(14)28)29-25(32)20-21(26(29)33)27(34-22(20)15-7-3-2-4-8-15)23(30)17-9-5-6-10-18(17)24(27)31/h2-13,22,32-33H,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Cubist Pharmaceuticals Inc. Curated by ChEMBL					Assay Description Inhibitory activity against human phenylalanyl-tRNA synthetase was determined				Bioorg Med Chem Lett 14: 1339-42 (2004) Article DOI: 10.1016/j.bmcl.2003.11.081 BindingDB Entry DOI: 10.7270/Q2PR7VDS
					More data for this Ligand-Target Pair
Phenylalanyl-tRNA synthetase alpha chain (Streptococcus pyogenes serotype M18)	BDBM50140707 (5-(3-chloro-4-methylphenyl)-3-phenyl-(3R,3aS,6aR)-...) Show SMILES Cc1ccc(cc1Cl)-n1c(O)c2C(OC3(C(=O)c4ccccc4C3=O)c2c1O)c1ccccc1 Show InChI InChI=1S/C27H18ClNO5/c1-14-11-12-16(13-19(14)28)29-25(32)20-21(26(29)33)27(34-22(20)15-7-3-2-4-8-15)23(30)17-9-5-6-10-18(17)24(27)31/h2-13,22,32-33H,1H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	70	n/a	n/a	n/a	n/a	n/a	n/a
Cubist Pharmaceuticals Inc. Curated by ChEMBL					Assay Description Inhibitory activity against phenylalanyl-tRNA synthetase from Staphylococcus aureus				Bioorg Med Chem Lett 14: 1339-42 (2004) Article DOI: 10.1016/j.bmcl.2003.11.081 BindingDB Entry DOI: 10.7270/Q2PR7VDS
					More data for this Ligand-Target Pair
Phenylalanyl-tRNA synthetase alpha chain (Streptococcus pyogenes serotype M18)	BDBM50140707 (5-(3-chloro-4-methylphenyl)-3-phenyl-(3R,3aS,6aR)-...) Show SMILES Cc1ccc(cc1Cl)-n1c(O)c2C(OC3(C(=O)c4ccccc4C3=O)c2c1O)c1ccccc1 Show InChI InChI=1S/C27H18ClNO5/c1-14-11-12-16(13-19(14)28)29-25(32)20-21(26(29)33)27(34-22(20)15-7-3-2-4-8-15)23(30)17-9-5-6-10-18(17)24(27)31/h2-13,22,32-33H,1H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.37E+4	n/a	n/a	n/a	n/a	n/a	n/a
Cubist Pharmaceuticals Inc. Curated by ChEMBL					Assay Description Inhibitory activity against phenylalanyl-tRNA synthetase from Enterococcus faecalis				Bioorg Med Chem Lett 14: 1339-42 (2004) Article DOI: 10.1016/j.bmcl.2003.11.081 BindingDB Entry DOI: 10.7270/Q2PR7VDS
					More data for this Ligand-Target Pair
Phenylalanyl-tRNA synthetase alpha chain (Streptococcus pyogenes serotype M18)	BDBM50140707 (5-(3-chloro-4-methylphenyl)-3-phenyl-(3R,3aS,6aR)-...) Show SMILES Cc1ccc(cc1Cl)-n1c(O)c2C(OC3(C(=O)c4ccccc4C3=O)c2c1O)c1ccccc1 Show InChI InChI=1S/C27H18ClNO5/c1-14-11-12-16(13-19(14)28)29-25(32)20-21(26(29)33)27(34-22(20)15-7-3-2-4-8-15)23(30)17-9-5-6-10-18(17)24(27)31/h2-13,22,32-33H,1H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Cubist Pharmaceuticals Inc. Curated by ChEMBL					Assay Description Inhibitory activity against phenylalanyl-tRNA synthetase from Staphylococcus aureus				Bioorg Med Chem Lett 14: 1339-42 (2004) Article DOI: 10.1016/j.bmcl.2003.11.081 BindingDB Entry DOI: 10.7270/Q2PR7VDS
					More data for this Ligand-Target Pair
Phenylalanyl-tRNA synthetase mitochondrial (Homo sapiens (Human))	BDBM50140707 (5-(3-chloro-4-methylphenyl)-3-phenyl-(3R,3aS,6aR)-...) Show SMILES Cc1ccc(cc1Cl)-n1c(O)c2C(OC3(C(=O)c4ccccc4C3=O)c2c1O)c1ccccc1 Show InChI InChI=1S/C27H18ClNO5/c1-14-11-12-16(13-19(14)28)29-25(32)20-21(26(29)33)27(34-22(20)15-7-3-2-4-8-15)23(30)17-9-5-6-10-18(17)24(27)31/h2-13,22,32-33H,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Cubist Pharmaceuticals Inc. Curated by ChEMBL					Assay Description Inhibitory activity against phenylalanyl-tRNA synthetase from Enterococcus faecalis				Bioorg Med Chem Lett 14: 1339-42 (2004) Article DOI: 10.1016/j.bmcl.2003.11.081 BindingDB Entry DOI: 10.7270/Q2PR7VDS
					More data for this Ligand-Target Pair