Compile Data Set for Download or QSAR

Found 3 hits Enz. Inhib. hit(s) with Target = 'Gag-Pol polyprotein [489-587]' and Ligand = 'BDBM1136'   

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
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM1136 ((4R,5R,6R)-6-benzyl-5-hydroxy-1-(1H-indazol-5-ylme...) Show SMILES O[C@@H]1[C@@H](CCc2ccccc2)NC(=O)N(Cc2ccc3[nH]ncc3c2)[C@@H]1Cc1ccccc1 |r| Show InChI InChI=1S/C27H28N4O2/c32-26-24(14-11-19-7-3-1-4-8-19)29-27(33)31(25(26)16-20-9-5-2-6-10-20)18-21-12-13-23-22(15-21)17-28-30-23/h1-10,12-13,15,17,24-26,32H,11,14,16,18H2,(H,28,30)(H,29,33)/t24-,25-,26-/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	1.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Florida Curated by ChEMBL					Assay Description Inhibitory activity of compound against HIV-1 aspartyl protease.				Bioorg Med Chem Lett 12: 3453-7 (2002) BindingDB Entry DOI: 10.7270/Q2B27WG3
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM1136 ((4R,5R,6R)-6-benzyl-5-hydroxy-1-(1H-indazol-5-ylme...) Show SMILES O[C@@H]1[C@@H](CCc2ccccc2)NC(=O)N(Cc2ccc3[nH]ncc3c2)[C@@H]1Cc1ccccc1 |r| Show InChI InChI=1S/C27H28N4O2/c32-26-24(14-11-19-7-3-1-4-8-19)29-27(33)31(25(26)16-20-9-5-2-6-10-20)18-21-12-13-23-22(15-21)17-28-30-23/h1-10,12-13,15,17,24-26,32H,11,14,16,18H2,(H,28,30)(H,29,33)/t24-,25-,26-/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	1.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
DuPont Pharmaceuticals Company					Assay Description Inhibition constant of HIV protease inhibitors				J Med Chem 42: 135-52 (1999) Article DOI: 10.1021/jm9803626 BindingDB Entry DOI: 10.7270/Q28050S9
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM1136 ((4R,5R,6R)-6-benzyl-5-hydroxy-1-(1H-indazol-5-ylme...) Show SMILES O[C@@H]1[C@@H](CCc2ccccc2)NC(=O)N(Cc2ccc3[nH]ncc3c2)[C@@H]1Cc1ccccc1 |r| Show InChI InChI=1S/C27H28N4O2/c32-26-24(14-11-19-7-3-1-4-8-19)29-27(33)31(25(26)16-20-9-5-2-6-10-20)18-21-12-13-23-22(15-21)17-28-30-23/h1-10,12-13,15,17,24-26,32H,11,14,16,18H2,(H,28,30)(H,29,33)/t24-,25-,26-/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	1.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Missouri-St. Louis Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 protease				J Med Chem 45: 973-83 (2002) Article DOI: 10.1021/jm010417v BindingDB Entry DOI: 10.7270/Q2JH3PX8
					More data for this Ligand-Target Pair