null

SMILES: OC(=O)c1cc(Br)ccc1NC(=O)Cc1cccc(c1)C(=O)Nc1ccc(Br)cc1C(O)=O

InChI Key: InChIKey=RLLUGLRPWGPLPZ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50071760   

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)	BDBM50071760 (5-bromo-2-{[(3-{[(4-bromo-2-carboxyphenyl)amino]ca...) Show SMILES OC(=O)c1cc(Br)ccc1NC(=O)Cc1cccc(c1)C(=O)Nc1ccc(Br)cc1C(O)=O Show InChI InChI=1S/C23H16Br2N2O6/c24-14-4-6-18(16(10-14)22(30)31)26-20(28)9-12-2-1-3-13(8-12)21(29)27-19-7-5-15(25)11-17(19)23(32)33/h1-8,10-11H,9H2,(H,26,28)(H,27,29)(H,30,31)(H,32,33)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	2.10E+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
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50071760 (5-bromo-2-{[(3-{[(4-bromo-2-carboxyphenyl)amino]ca...) Show SMILES OC(=O)c1cc(Br)ccc1NC(=O)Cc1cccc(c1)C(=O)Nc1ccc(Br)cc1C(O)=O Show InChI InChI=1S/C23H16Br2N2O6/c24-14-4-6-18(16(10-14)22(30)31)26-20(28)9-12-2-1-3-13(8-12)21(29)27-19-7-5-15(25)11-17(19)23(32)33/h1-8,10-11H,9H2,(H,26,28)(H,27,29)(H,30,31)(H,32,33)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	1.50E+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-1 reverse transcriptase				Bioorg Med Chem Lett 8: 2623-8 (1999) BindingDB Entry DOI: 10.7270/Q2RF5T6F
					More data for this Ligand-Target Pair