null

SMILES: Oc1cc(cc2cc(cc(O)c12)S([O-])(=O)=O)S([O-])(=O)=O

InChI Key: InChIKey=HLVXFWDLRHCZEI-UHFFFAOYSA-L

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50143421   

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
Tyrosine-protein phosphatase 1 (Saccharomyces cerevisiae)	BDBM50143421 (CHEMBL425511 | Di sodium; 4,5-Dihydroxy-7-sulfo-na...) Show SMILES Oc1cc(cc2cc(cc(O)c12)S([O-])(=O)=O)S([O-])(=O)=O Show InChI InChI=1S/C10H8O8S2/c11-8-3-6(19(13,14)15)1-5-2-7(20(16,17)18)4-9(12)10(5)8/h1-4,11-12H,(H,13,14,15)(H,16,17,18)/p-2	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Inha University Curated by ChEMBL					Assay Description Inhibitory activity against Saccharomyces cerevisiae Tyrosine phosphatase 1				Bioorg Med Chem Lett 14: 1923-6 (2004) Article DOI: 10.1016/j.bmcl.2004.01.079 BindingDB Entry DOI: 10.7270/Q2JS9R01
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50143421 (CHEMBL425511 | Di sodium; 4,5-Dihydroxy-7-sulfo-na...) Show SMILES Oc1cc(cc2cc(cc(O)c12)S([O-])(=O)=O)S([O-])(=O)=O Show InChI InChI=1S/C10H8O8S2/c11-8-3-6(19(13,14)15)1-5-2-7(20(16,17)18)4-9(12)10(5)8/h1-4,11-12H,(H,13,14,15)(H,16,17,18)/p-2	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.01E+5	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
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50143421 (CHEMBL425511 | Di sodium; 4,5-Dihydroxy-7-sulfo-na...) Show SMILES Oc1cc(cc2cc(cc(O)c12)S([O-])(=O)=O)S([O-])(=O)=O Show InChI InChI=1S/C10H8O8S2/c11-8-3-6(19(13,14)15)1-5-2-7(20(16,17)18)4-9(12)10(5)8/h1-4,11-12H,(H,13,14,15)(H,16,17,18)/p-2	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.25E+5	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
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50143421 (CHEMBL425511 | Di sodium; 4,5-Dihydroxy-7-sulfo-na...) Show SMILES Oc1cc(cc2cc(cc(O)c12)S([O-])(=O)=O)S([O-])(=O)=O Show InChI InChI=1S/C10H8O8S2/c11-8-3-6(19(13,14)15)1-5-2-7(20(16,17)18)4-9(12)10(5)8/h1-4,11-12H,(H,13,14,15)(H,16,17,18)/p-2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Inha University Curated by ChEMBL					Assay Description Inhibition of human PTPase 1B				Bioorg Med Chem Lett 14: 1923-6 (2004) Article DOI: 10.1016/j.bmcl.2004.01.079 BindingDB Entry DOI: 10.7270/Q2JS9R01
					More data for this Ligand-Target Pair