null

SMILES: OC(=O)c1ccccc1NC(=O)CCCCC(=O)Nc1ccccc1C(O)=O

InChI Key: InChIKey=WFLXRCUOXLSGPW-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50071763   

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)	BDBM50071763 (2-({6-[(2-carboxyphenyl)amino]-6-oxohexanoyl}amino...) Show SMILES OC(=O)c1ccccc1NC(=O)CCCCC(=O)Nc1ccccc1C(O)=O Show InChI InChI=1S/C20H20N2O6/c23-17(21-15-9-3-1-7-13(15)19(25)26)11-5-6-12-18(24)22-16-10-4-2-8-14(16)20(27)28/h1-4,7-10H,5-6,11-12H2,(H,21,23)(H,22,24)(H,25,26)(H,27,28)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	9.00E+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)	BDBM50071763 (2-({6-[(2-carboxyphenyl)amino]-6-oxohexanoyl}amino...) Show SMILES OC(=O)c1ccccc1NC(=O)CCCCC(=O)Nc1ccccc1C(O)=O Show InChI InChI=1S/C20H20N2O6/c23-17(21-15-9-3-1-7-13(15)19(25)26)11-5-6-12-18(24)22-16-10-4-2-8-14(16)20(27)28/h1-4,7-10H,5-6,11-12H2,(H,21,23)(H,22,24)(H,25,26)(H,27,28)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	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-2 reverse transcriptase				Bioorg Med Chem Lett 8: 2623-8 (1999) BindingDB Entry DOI: 10.7270/Q2RF5T6F
					More data for this Ligand-Target Pair