null

SMILES Oc1ccc(cc1O)C(=O)Cn1ccnc1

InChI Key InChIKey=JHQYDDFNYJJOIA-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 41887   

TargetAlkaline phosphatase, germ cell type(Homo sapiens (Human))
Sanford-Burnham Center for Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM41887(1-(3,4-dihydroxyphenyl)-2-(1-imidazolyl)ethanone;h...)copy SMILEScopy InChI
Affinity DataIC50: 3.02E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JQ0ZDSPCBioAssay
TargetAlkaline phosphatase, germ cell type(Homo sapiens (Human))
Sanford-Burnham Center for Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM41887(1-(3,4-dihydroxyphenyl)-2-(1-imidazolyl)ethanone;h...)copy SMILEScopy InChI
Affinity DataIC50: 1.85E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JQ0ZDSPCBioAssay
TargetAlkaline phosphatase, tissue-nonspecific isozyme(Homo sapiens (Human))
Burnham Center for Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM41887(1-(3,4-dihydroxyphenyl)-2-(1-imidazolyl)ethanone;h...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Sanford-Burnham Center for Chemical Genomics (SBCCG) Sanford-Burnham Medical Research Institute (SBMRI, San Diego, CA) NIH Molecular Libraries Screen...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2CR5RRGPCBioAssay
TargetAlkaline phosphatase, tissue-nonspecific isozyme(Homo sapiens (Human))
Burnham Center for Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM41887(1-(3,4-dihydroxyphenyl)-2-(1-imidazolyl)ethanone;h...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Sanford-Burnham Center for Chemical Genomics (SBCCG) Sanford-Burnham Medical Research Institute (SBMRI, San Diego, CA) NIH Molecular Libraries Screen...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2CR5RRGPCBioAssay
TargetAlkaline phosphatase, germ cell type(Homo sapiens (Human))
Sanford-Burnham Center for Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM41887(1-(3,4-dihydroxyphenyl)-2-(1-imidazolyl)ethanone;h...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of GCAP by analogous luminescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6JHRPubMed
TargetAlkaline phosphatase, germ cell type(Homo sapiens (Human))
Sanford-Burnham Center for Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM41887(1-(3,4-dihydroxyphenyl)-2-(1-imidazolyl)ethanone;h...)copy SMILEScopy InChI
Affinity DataIC50: 2.11E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29S1PG8PCBioAssay
TargetPhospholipase A-2-activating protein(Homo sapiens (Human))
Human BioMolecular Research Institute

Curated by ChEMBL
LigandPNGBDBM41887(1-(3,4-dihydroxyphenyl)-2-(1-imidazolyl)ethanone;h...)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of PLAP by analogous luminescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6JHRPubMed
TargetAlkaline phosphatase, tissue-nonspecific isozyme(Homo sapiens (Human))
Burnham Center for Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM41887(1-(3,4-dihydroxyphenyl)-2-(1-imidazolyl)ethanone;h...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of TNAP by analogous luminescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6JHRPubMed
TargetIntestinal-type alkaline phosphatase(Homo sapiens (Human))
Human BioMolecular Research Institute

Curated by ChEMBL
LigandPNGBDBM41887(1-(3,4-dihydroxyphenyl)-2-(1-imidazolyl)ethanone;h...)copy SMILEScopy InChI
Affinity DataIC50: 3.02E+4nMAssay Description:Inhibition of IAP by analogous luminescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6JHRPubMed
TargetAlkaline phosphatase, germ cell type(Homo sapiens (Human))
Sanford-Burnham Center for Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM41887(1-(3,4-dihydroxyphenyl)-2-(1-imidazolyl)ethanone;h...)copy SMILEScopy InChI
Affinity DataIC50: 5.37E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29S1PG8PCBioAssay