BDBM50177408 4-(hydroxymethyl)phenol::4-Hydroxybenzyl alcohol::4HBA::CHEMBL202132::parahydroxybenzyl alcohol

SMILES: OCc1ccc(O)cc1

InChI Key: InChIKey=BVJSUAQZOZWCKN-UHFFFAOYSA-N

Data: 5 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 5 hits for monomerid = 50177408   

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 (Mus musculus (Mouse))	BDBM50177408 (4-(hydroxymethyl)phenol | 4-Hydroxybenzyl alcohol ...) Show SMILES OCc1ccc(O)cc1 Show InChI InChI=1S/C7H8O2/c8-5-6-1-3-7(9)4-2-6/h1-4,8-9H,5H2	UniProtKB/SwissProt UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	6.50E+5	n/a	n/a	n/a	n/a	6.8	25
National Tsing Hua University					Assay Description The enzyme activity was monitored by dopachrome formation at 475nm for an appropriate period.				J Enzyme Inhib Med Chem 23: 526-34 (2008) Article DOI: 10.1080/14756360701654894 BindingDB Entry DOI: 10.7270/Q29885MB
					More data for this Ligand-Target Pair
Tyrosinase (Agaricus bisporus (Common mushroom))	BDBM50177408 (4-(hydroxymethyl)phenol | 4-Hydroxybenzyl alcohol ...) Show SMILES OCc1ccc(O)cc1 Show InChI InChI=1S/C7H8O2/c8-5-6-1-3-7(9)4-2-6/h1-4,8-9H,5H2	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	3.50E+5	n/a	n/a	n/a	n/a	6.8	25
National Tsing Hua University					Assay Description The enzyme activity was monitored by dopachrome formation at 475nm for an appropriate period.				J Enzyme Inhib Med Chem 23: 526-34 (2008) Article DOI: 10.1080/14756360701654894 BindingDB Entry DOI: 10.7270/Q29885MB
					More data for this Ligand-Target Pair
Tyrosinase (Agaricus bisporus (Common mushroom))	BDBM50177408 (4-(hydroxymethyl)phenol | 4-Hydroxybenzyl alcohol ...) Show SMILES OCc1ccc(O)cc1 Show InChI InChI=1S/C7H8O2/c8-5-6-1-3-7(9)4-2-6/h1-4,8-9H,5H2	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Medicinal Plant Development Curated by ChEMBL					Assay Description Inhibition of mushroom tyrosinase using L-DOPA after 10 mins by ELISA reader				J Nat Prod 74: 1009-14 (2011) Article DOI: 10.1021/np100900k BindingDB Entry DOI: 10.7270/Q2TQ61WN
					More data for this Ligand-Target Pair
Gamma-amino-N-butyrate transaminase (Homo sapiens (Human))	BDBM50177408 (4-(hydroxymethyl)phenol | 4-Hydroxybenzyl alcohol ...) Show SMILES OCc1ccc(O)cc1 Show InChI InChI=1S/C7H8O2/c8-5-6-1-3-7(9)4-2-6/h1-4,8-9H,5H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against GABAT				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair
Succinate semialdehyde dehydrogenase (Homo sapiens (Human))	BDBM50177408 (4-(hydroxymethyl)phenol | 4-Hydroxybenzyl alcohol ...) Show SMILES OCc1ccc(O)cc1 Show InChI InChI=1S/C7H8O2/c8-5-6-1-3-7(9)4-2-6/h1-4,8-9H,5H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against SSADH				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair