null

SMILES: CC(=O)c1cc2cc(oc2cc1O)-c1coc2cc(O)c(cc12)C(C)=O

InChI Key: InChIKey=XEPLVRZUMGHVMU-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50198350   

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 non-receptor type 1 (Homo sapiens (Human))	BDBM50198350 (1-(5-acetyl-4,4'-dihydroxy-2',3'-dihydro-[2,3']bib...) Show SMILES CC(=O)c1cc2cc(oc2cc1O)-c1coc2cc(O)c(cc12)C(C)=O Show InChI InChI=1S/C20H14O6/c1-9(21)12-3-11-4-20(26-18(11)6-16(12)23)15-8-25-19-7-17(24)13(10(2)22)5-14(15)19/h3-8,23-24H,1-2H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.70E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Central Drug Research Institute Curated by ChEMBL					Assay Description Inhibition of PTP1B				Bioorg Med Chem 15: 727-34 (2006) Article DOI: 10.1016/j.bmc.2006.10.053 BindingDB Entry DOI: 10.7270/Q2CR5T1W
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50198350 (1-(5-acetyl-4,4'-dihydroxy-2',3'-dihydro-[2,3']bib...) Show SMILES CC(=O)c1cc2cc(oc2cc1O)-c1coc2cc(O)c(cc12)C(C)=O Show InChI InChI=1S/C20H14O6/c1-9(21)12-3-11-4-20(26-18(11)6-16(12)23)15-8-25-19-7-17(24)13(10(2)22)5-14(15)19/h3-8,23-24H,1-2H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.10E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Central Drug Research Institute Curated by ChEMBL					Assay Description Inhibition of PTP1B in presence of 0.01% Triton X-100				Bioorg Med Chem 15: 727-34 (2006) Article DOI: 10.1016/j.bmc.2006.10.053 BindingDB Entry DOI: 10.7270/Q2CR5T1W
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50198350 (1-(5-acetyl-4,4'-dihydroxy-2',3'-dihydro-[2,3']bib...) Show SMILES CC(=O)c1cc2cc(oc2cc1O)-c1coc2cc(O)c(cc12)C(C)=O Show InChI InChI=1S/C20H14O6/c1-9(21)12-3-11-4-20(26-18(11)6-16(12)23)15-8-25-19-7-17(24)13(10(2)22)5-14(15)19/h3-8,23-24H,1-2H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Central Drug Research Institute Curated by ChEMBL					Assay Description Inhibition of PTP1B				Bioorg Med Chem 15: 727-34 (2006) Article DOI: 10.1016/j.bmc.2006.10.053 BindingDB Entry DOI: 10.7270/Q2CR5T1W
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50198350 (1-(5-acetyl-4,4'-dihydroxy-2',3'-dihydro-[2,3']bib...) Show SMILES CC(=O)c1cc2cc(oc2cc1O)-c1coc2cc(O)c(cc12)C(C)=O Show InChI InChI=1S/C20H14O6/c1-9(21)12-3-11-4-20(26-18(11)6-16(12)23)15-8-25-19-7-17(24)13(10(2)22)5-14(15)19/h3-8,23-24H,1-2H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.13E+4	n/a	n/a	n/a	n/a	n/a	n/a
Central Drug Research Institute Curated by ChEMBL					Assay Description Inhibition of PTP1B in presence of 0.01% Triton X-100				Bioorg Med Chem 15: 727-34 (2006) Article DOI: 10.1016/j.bmc.2006.10.053 BindingDB Entry DOI: 10.7270/Q2CR5T1W
					More data for this Ligand-Target Pair