Compile Data Set for Download or QSAR

Found 2 hits of ic50 for monomerid = 50126991   

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
17-beta-hydroxysteroid dehydrogenase type 1 (Homo sapiens (Human))	BDBM50126991 (CHEMBL3629446) Show SMILES Oc1cccc(c1)C(=O)c1ccc(s1)-c1cccc(NS(=O)(=O)c2ccccc2[N+]([O-])=O)c1 Show InChI InChI=1S/C23H16N2O6S2/c26-18-8-4-6-16(14-18)23(27)21-12-11-20(32-21)15-5-3-7-17(13-15)24-33(30,31)22-10-2-1-9-19(22)25(28)29/h1-14,24,26H	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	32	n/a	n/a	n/a	n/a	n/a	n/a
Saarland University Curated by ChEMBL					Assay Description Inhibition of human placental cytosolic 17beta HSD1 using unlabeled- and labelled [2,4,6,7-3H]-E1 as substrate incubated for 10 mins by HPLC analysis				Eur J Med Chem 103: 56-68 (2015) Article DOI: 10.1016/j.ejmech.2015.08.030 BindingDB Entry DOI: 10.7270/Q22V2HXX
					More data for this Ligand-Target Pair
17-beta-hydroxysteroid dehydrogenase type 2 (Homo sapiens (Human))	BDBM50126991 (CHEMBL3629446) Show SMILES Oc1cccc(c1)C(=O)c1ccc(s1)-c1cccc(NS(=O)(=O)c2ccccc2[N+]([O-])=O)c1 Show InChI InChI=1S/C23H16N2O6S2/c26-18-8-4-6-16(14-18)23(27)21-12-11-20(32-21)15-5-3-7-17(13-15)24-33(30,31)22-10-2-1-9-19(22)25(28)29/h1-14,24,26H	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	148	n/a	n/a	n/a	n/a	n/a	n/a
Saarland University Curated by ChEMBL					Assay Description Inhibition of human placental microsomal 17beta HSD2 using unlabeled- and labelled [2,4,6,7-3H]-E2 as substrate incubated for 20 mins by HPLC analysi...				Eur J Med Chem 103: 56-68 (2015) Article DOI: 10.1016/j.ejmech.2015.08.030 BindingDB Entry DOI: 10.7270/Q22V2HXX
					More data for this Ligand-Target Pair