BDBM50187503 2-Methylresorcinol::CHEMBL2332773

SMILES: Cc1c(O)cccc1O

InChI Key: InChIKey=ZTMADXFOCUXMJE-UHFFFAOYSA-N

Data: 2 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50187503   

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
Tyrosinase (Agaricus bisporus (Common mushroom))	BDBM50187503 (2-Methylresorcinol | CHEMBL2332773) Show SMILES Cc1c(O)cccc1O Show InChI InChI=1S/C7H8O2/c1-5-6(8)3-2-4-7(5)9/h2-4,8-9H,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	7.17E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Murcia Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-dopa as substrate assessed as diphenolase activity by spectrophotometric analysis				Bioorg Med Chem 24: 4434-4443 (2016) BindingDB Entry DOI: 10.7270/Q24F1SP6
					More data for this Ligand-Target Pair
Tyrosinase (Agaricus bisporus (Common mushroom))	BDBM50187503 (2-Methylresorcinol | CHEMBL2332773) Show SMILES Cc1c(O)cccc1O Show InChI InChI=1S/C7H8O2/c1-5-6(8)3-2-4-7(5)9/h2-4,8-9H,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.42E+6	n/a	n/a	n/a	n/a	n/a	n/a
University of Murcia Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-tyrosine as substrate assessed as monophenolase activity by spectrophotometric analysis				Bioorg Med Chem 24: 4434-4443 (2016) BindingDB Entry DOI: 10.7270/Q24F1SP6
					More data for this Ligand-Target Pair