null

SMILES: OC(=O)c1cc(Br)ccc1NC(=O)CCCC(=O)Nc1ccc(Br)cc1C(O)=O

InChI Key: InChIKey=JVSZLRWEDCMENT-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50071762   

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)	BDBM50071762 (5-bromo-2-({5-[(4-bromo-2-carboxyphenyl)amino]-5-o...) Show SMILES OC(=O)c1cc(Br)ccc1NC(=O)CCCC(=O)Nc1ccc(Br)cc1C(O)=O Show InChI InChI=1S/C19H16Br2N2O6/c20-10-4-6-14(12(8-10)18(26)27)22-16(24)2-1-3-17(25)23-15-7-5-11(21)9-13(15)19(28)29/h4-9H,1-3H2,(H,22,24)(H,23,25)(H,26,27)(H,28,29)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7.30E+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
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50071762 (5-bromo-2-({5-[(4-bromo-2-carboxyphenyl)amino]-5-o...) Show SMILES OC(=O)c1cc(Br)ccc1NC(=O)CCCC(=O)Nc1ccc(Br)cc1C(O)=O Show InChI InChI=1S/C19H16Br2N2O6/c20-10-4-6-14(12(8-10)18(26)27)22-16(24)2-1-3-17(25)23-15-7-5-11(21)9-13(15)19(28)29/h4-9H,1-3H2,(H,22,24)(H,23,25)(H,26,27)(H,28,29)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.00E+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