Compile Data Set for Download or QSAR

Found 3 hits of ic50 for monomerid = 50075161   

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
Capsid scaffolding protein (Human herpesvirus 6A (strain Uganda-1102) (HHV-6 v...)	BDBM50075161 ((E)-3-(4-Dimethylamino-phenyl)-N-[(S)-1-(5-methyl-...) Show SMILES C[C@H](NC(=O)\C=C\c1ccc(cc1)N(C)C)c1nc2scc(C)c2c(=O)o1 Show InChI InChI=1S/C20H21N3O3S/c1-12-11-27-19-17(12)20(25)26-18(22-19)13(2)21-16(24)10-7-14-5-8-15(9-6-14)23(3)4/h5-11,13H,1-4H3,(H,21,24)/b10-7+/t13-/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	38	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals Curated by ChEMBL					Assay Description Inhibitory activity against Varicella Zoster Virus (VZV) protease was determined using quenched fluorescence assay				Bioorg Med Chem Lett 9: 443-8 (1999) BindingDB Entry DOI: 10.7270/Q2ZC822V
					More data for this Ligand-Target Pair
Capsid scaffolding protein (Human herpesvirus 2 (strain HG52) (HHV-2) (Human h...)	BDBM50075161 ((E)-3-(4-Dimethylamino-phenyl)-N-[(S)-1-(5-methyl-...) Show SMILES C[C@H](NC(=O)\C=C\c1ccc(cc1)N(C)C)c1nc2scc(C)c2c(=O)o1 Show InChI InChI=1S/C20H21N3O3S/c1-12-11-27-19-17(12)20(25)26-18(22-19)13(2)21-16(24)10-7-14-5-8-15(9-6-14)23(3)4/h5-11,13H,1-4H3,(H,21,24)/b10-7+/t13-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	570	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals Curated by ChEMBL					Assay Description Inhibitory activity against herpes simplex virus type 2 (HSV-2) protease was determined using quenched fluorescence assay				Bioorg Med Chem Lett 9: 443-8 (1999) BindingDB Entry DOI: 10.7270/Q2ZC822V
					More data for this Ligand-Target Pair
Capsid scaffolding protein (Epstein-Barr virus (strain B95-8) (HHV-4) (Human h...)	BDBM50075161 ((E)-3-(4-Dimethylamino-phenyl)-N-[(S)-1-(5-methyl-...) Show SMILES C[C@H](NC(=O)\C=C\c1ccc(cc1)N(C)C)c1nc2scc(C)c2c(=O)o1 Show InChI InChI=1S/C20H21N3O3S/c1-12-11-27-19-17(12)20(25)26-18(22-19)13(2)21-16(24)10-7-14-5-8-15(9-6-14)23(3)4/h5-11,13H,1-4H3,(H,21,24)/b10-7+/t13-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals Curated by ChEMBL					Assay Description Inhibitory activity against cytomegalovirus (CMV) protease was determined using quenched fluorescence assay				Bioorg Med Chem Lett 9: 443-8 (1999) BindingDB Entry DOI: 10.7270/Q2ZC822V
					More data for this Ligand-Target Pair