null

SMILES: OC(=O)c1cc(O)ccc1NC(=O)CCCCC(=O)Nc1ccc(O)cc1C(O)=O

InChI Key: InChIKey=AYJXEWMGOQLVRU-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50071767   

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)	BDBM50071767 (2-({6-[(2-carboxy-4-hydroxyphenyl)amino]-6-oxohexa...) Show SMILES OC(=O)c1cc(O)ccc1NC(=O)CCCCC(=O)Nc1ccc(O)cc1C(O)=O Show InChI InChI=1S/C20H20N2O8/c23-11-5-7-15(13(9-11)19(27)28)21-17(25)3-1-2-4-18(26)22-16-8-6-12(24)10-14(16)20(29)30/h5-10,23-24H,1-4H2,(H,21,25)(H,22,26)(H,27,28)(H,29,30)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	6.70E+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-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)	BDBM50071767 (2-({6-[(2-carboxy-4-hydroxyphenyl)amino]-6-oxohexa...) Show SMILES OC(=O)c1cc(O)ccc1NC(=O)CCCCC(=O)Nc1ccc(O)cc1C(O)=O Show InChI InChI=1S/C20H20N2O8/c23-11-5-7-15(13(9-11)19(27)28)21-17(25)3-1-2-4-18(26)22-16-8-6-12(24)10-14(16)20(29)30/h5-10,23-24H,1-4H2,(H,21,25)(H,22,26)(H,27,28)(H,29,30)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.20E+5	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