Compile Data Set for Download or QSAR

Found 2 hits of ec50 for monomerid = 50171975   

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
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50171975 (3-{4-[2-(5-Ethyl-10-methyl-11-oxo-10,11-dihydro-5H...) Show SMILES CCN1c2ncccc2N(C)C(=O)c2cc(CCOc3ccc(CCC(O)=O)cc3C)cnc12 Show InChI InChI=1S/C26H28N4O4/c1-4-30-24-20(26(33)29(3)21-6-5-12-27-25(21)30)15-19(16-28-24)11-13-34-22-9-7-18(14-17(22)2)8-10-23(31)32/h5-7,9,12,14-16H,4,8,10-11,13H2,1-3H3,(H,31,32)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	5.5	n/a	n/a	n/a	n/a
Boehringer Ingelheim (Canada) Ltd. Curated by ChEMBL					Assay Description Effective concentration towards HIV-1 wild type reverse transcriptase activity by 50% measured in cellular assay				J Med Chem 48: 5580-8 (2005) Article DOI: 10.1021/jm050255t BindingDB Entry DOI: 10.7270/Q29K49RC
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50171975 (3-{4-[2-(5-Ethyl-10-methyl-11-oxo-10,11-dihydro-5H...) Show SMILES CCN1c2ncccc2N(C)C(=O)c2cc(CCOc3ccc(CCC(O)=O)cc3C)cnc12 Show InChI InChI=1S/C26H28N4O4/c1-4-30-24-20(26(33)29(3)21-6-5-12-27-25(21)30)15-19(16-28-24)11-13-34-22-9-7-18(14-17(22)2)8-10-23(31)32/h5-7,9,12,14-16H,4,8,10-11,13H2,1-3H3,(H,31,32)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	101	n/a	n/a	n/a	n/a
Boehringer Ingelheim (Canada) Ltd. Curated by ChEMBL					Assay Description Effective concentration of the compound towards HIV-1 K103N/Y181C mutant reverse transcriptase activity by 50% measured in cellular assay				J Med Chem 48: 5580-8 (2005) Article DOI: 10.1021/jm050255t BindingDB Entry DOI: 10.7270/Q29K49RC
					More data for this Ligand-Target Pair