null

SMILES: O=c1cc(oc2cc3occc3cc12)-c1ccccc1

InChI Key: InChIKey=RIFWZGCPXPFPAY-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50198348   

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))	BDBM50198348 (7-phenyl-furo[3,2-g]chromen-5-one | CHEMBL388814) Show SMILES O=c1cc(oc2cc3occc3cc12)-c1ccccc1 Show InChI InChI=1S/C17H10O3/c18-14-9-16(11-4-2-1-3-5-11)20-17-10-15-12(6-7-19-15)8-13(14)17/h1-10H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.50E+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))	BDBM50198348 (7-phenyl-furo[3,2-g]chromen-5-one | CHEMBL388814) Show SMILES O=c1cc(oc2cc3occc3cc12)-c1ccccc1 Show InChI InChI=1S/C17H10O3/c18-14-9-16(11-4-2-1-3-5-11)20-17-10-15-12(6-7-19-15)8-13(14)17/h1-10H	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.70E+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))	BDBM50198348 (7-phenyl-furo[3,2-g]chromen-5-one | CHEMBL388814) Show SMILES O=c1cc(oc2cc3occc3cc12)-c1ccccc1 Show InChI InChI=1S/C17H10O3/c18-14-9-16(11-4-2-1-3-5-11)20-17-10-15-12(6-7-19-15)8-13(14)17/h1-10H	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	6.13E+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
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50198348 (7-phenyl-furo[3,2-g]chromen-5-one | CHEMBL388814) Show SMILES O=c1cc(oc2cc3occc3cc12)-c1ccccc1 Show InChI InChI=1S/C17H10O3/c18-14-9-16(11-4-2-1-3-5-11)20-17-10-15-12(6-7-19-15)8-13(14)17/h1-10H	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	9.40E+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