null

SMILES: CC(=O)Nc1cc(cc2cc(cc(OC(C)=O)c12)S([O-])(=O)=O)S([O-])(=O)=O

InChI Key: InChIKey=FBZQMQAHEDKOQX-UHFFFAOYSA-L

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50368495   

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)	BDBM50368495 (CHEMBL1744149) Show SMILES CC(=O)Nc1cc(cc2cc(cc(OC(C)=O)c12)S([O-])(=O)=O)S([O-])(=O)=O Show InChI InChI=1S/C14H13NO9S2/c1-7(16)15-12-5-10(25(18,19)20)3-9-4-11(26(21,22)23)6-13(14(9)12)24-8(2)17/h3-6H,1-2H3,(H,15,16)(H,18,19,20)(H,21,22,23)/p-2	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Universityof Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of purified HIV-1 reverse transcriptase				J Med Chem 35: 4846-53 (1992) BindingDB Entry DOI: 10.7270/Q2M0461N
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50368495 (CHEMBL1744149) Show SMILES CC(=O)Nc1cc(cc2cc(cc(OC(C)=O)c12)S([O-])(=O)=O)S([O-])(=O)=O Show InChI InChI=1S/C14H13NO9S2/c1-7(16)15-12-5-10(25(18,19)20)3-9-4-11(26(21,22)23)6-13(14(9)12)24-8(2)17/h3-6H,1-2H3,(H,15,16)(H,18,19,20)(H,21,22,23)/p-2	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Universityof Illinois at Chicago Curated by ChEMBL					Assay Description Inhibition of purified HIV-2 reverse transcriptase				J Med Chem 35: 4846-53 (1992) BindingDB Entry DOI: 10.7270/Q2M0461N
					More data for this Ligand-Target Pair