null

SMILES: OC(=O)c1cc(Br)ccc1NC(=O)c1cccc(c1)C(=O)Nc1ccc(Br)cc1C(O)=O

InChI Key: InChIKey=IVTXHKFFXZJTSW-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50071780   

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
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50071780 (5-bromo-2-[(3-{[(4-bromo-2-carboxyphenyl)amino]car...) Show SMILES OC(=O)c1cc(Br)ccc1NC(=O)c1cccc(c1)C(=O)Nc1ccc(Br)cc1C(O)=O Show InChI InChI=1S/C22H14Br2N2O6/c23-13-4-6-17(15(9-13)21(29)30)25-19(27)11-2-1-3-12(8-11)20(28)26-18-7-5-14(24)10-16(18)22(31)32/h1-10H,(H,25,27)(H,26,28)(H,29,30)(H,31,32)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoWellcome Medicines Research Center Curated by ChEMBL					Assay Description Evaluated for inhibition of HIV-2 reverse transcriptase				Bioorg Med Chem Lett 8: 2623-8 (1999) BindingDB Entry DOI: 10.7270/Q2RF5T6F
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50071780 (5-bromo-2-[(3-{[(4-bromo-2-carboxyphenyl)amino]car...) Show SMILES OC(=O)c1cc(Br)ccc1NC(=O)c1cccc(c1)C(=O)Nc1ccc(Br)cc1C(O)=O Show InChI InChI=1S/C22H14Br2N2O6/c23-13-4-6-17(15(9-13)21(29)30)25-19(27)11-2-1-3-12(8-11)20(28)26-18-7-5-14(24)10-16(18)22(31)32/h1-10H,(H,25,27)(H,26,28)(H,29,30)(H,31,32)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoWellcome Medicines Research Center Curated by ChEMBL					Assay Description Evaluated for inhibition of HIV-1 reverse transcriptase				Bioorg Med Chem Lett 8: 2623-8 (1999) BindingDB Entry DOI: 10.7270/Q2RF5T6F
					More data for this Ligand-Target Pair