null

SMILES: OC(=O)c1cc(Br)ccc1NC(=O)c1ccc(nc1)C(=O)Nc1ccc(Br)cc1C(O)=O

InChI Key: InChIKey=NAOHAROVWHZEOI-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50071771   

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)	BDBM50071771 (5-bromo-2-{[(5-{[(4-bromo-2-carboxyphenyl)amino]ca...) Show SMILES OC(=O)c1cc(Br)ccc1NC(=O)c1ccc(nc1)C(=O)Nc1ccc(Br)cc1C(O)=O Show InChI InChI=1S/C21H13Br2N3O6/c22-11-2-5-15(13(7-11)20(29)30)25-18(27)10-1-4-17(24-9-10)19(28)26-16-6-3-12(23)8-14(16)21(31)32/h1-9H,(H,25,27)(H,26,28)(H,29,30)(H,31,32)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	3.50E+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)	BDBM50071771 (5-bromo-2-{[(5-{[(4-bromo-2-carboxyphenyl)amino]ca...) Show SMILES OC(=O)c1cc(Br)ccc1NC(=O)c1ccc(nc1)C(=O)Nc1ccc(Br)cc1C(O)=O Show InChI InChI=1S/C21H13Br2N3O6/c22-11-2-5-15(13(7-11)20(29)30)25-18(27)10-1-4-17(24-9-10)19(28)26-16-6-3-12(23)8-14(16)21(31)32/h1-9H,(H,25,27)(H,26,28)(H,29,30)(H,31,32)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	5.50E+3	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