null

SMILES: CC(C(=O)OCCO[N+]([O-])=O)c1ccc2c(c1)[nH]c1ccc(Cl)cc21

InChI Key: InChIKey=AKOHKZWHPPXXGH-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50272678   

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
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50272678 (2-(6-Chloro-9H-carbazol-2-yl)-propionic acid 2-nit...) Show SMILES CC(C(=O)OCCO[N+]([O-])=O)c1ccc2c(c1)[nH]c1ccc(Cl)cc21 Show InChI InChI=1S/C17H15ClN2O5/c1-10(17(21)24-6-7-25-20(22)23)11-2-4-13-14-9-12(18)3-5-15(14)19-16(13)8-11/h2-5,8-10,19H,6-7H2,1H3	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	6.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Université de Lille 2 Curated by ChEMBL					Assay Description Inhibition of COX2 in human whole blood				Bioorg Med Chem Lett 18: 4655-7 (2008) Article DOI: 10.1016/j.bmcl.2008.07.018 BindingDB Entry DOI: 10.7270/Q2G73DH6
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Homo sapiens (Human))	BDBM50272678 (2-(6-Chloro-9H-carbazol-2-yl)-propionic acid 2-nit...) Show SMILES CC(C(=O)OCCO[N+]([O-])=O)c1ccc2c(c1)[nH]c1ccc(Cl)cc21 Show InChI InChI=1S/C17H15ClN2O5/c1-10(17(21)24-6-7-25-20(22)23)11-2-4-13-14-9-12(18)3-5-15(14)19-16(13)8-11/h2-5,8-10,19H,6-7H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.10E+5	n/a	n/a	n/a	n/a	n/a	n/a
Université de Lille 2 Curated by ChEMBL					Assay Description Inhibition of COX1 in human whole blood				Bioorg Med Chem Lett 18: 4655-7 (2008) Article DOI: 10.1016/j.bmcl.2008.07.018 BindingDB Entry DOI: 10.7270/Q2G73DH6
					More data for this Ligand-Target Pair