BDBM50067033 (2E,6E)-2,6-bis(4-hydroxy-3-methoxybenzylidene)cyclohexanone::2,6-Bis((3-methoxy-4-hydroxyphenyl)methylene)-cyclohexanone::2,6-Bis-(4-hydroxy-3-methoxy-benzylidene)-cyclohexanone::2,6-Bis-[1-(4-hydroxy-3-methoxy-phenyl)-meth-(E)-ylidene]-cyclohexanone::2,6-bis(4-hydroxy-3-methoxybenzylidene)cyclohexanone::CHEMBL17205::Cyclovalone::US9187397, 38a::cid_1550234

SMILES COc1cc(\C=C2/CCC\C(=C/c3ccc(O)c(OC)c3)C2=O)ccc1O

InChI Key InChIKey=DHKKONBXGAAFTB-OTYYAQKOSA-N

Data  9 IC50  1 EC50

  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 = 50067033   

TargetNucleotide-binding oligomerization domain-containing protein 2(Homo sapiens (Human))
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM50067033((2E,6E)-2,6-bis(4-hydroxy-3-methoxybenzylidene)cyc...)
Affinity DataIC50:  3.75E+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 PCBioAssay
TargetNucleotide-binding oligomerization domain-containing protein 1(Homo sapiens (Human))
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM50067033((2E,6E)-2,6-bis(4-hydroxy-3-methoxybenzylidene)cyc...)
Affinity DataEC50:  4.94E+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 PCBioAssay
TargetTumor necrosis factor(Homo sapiens (Human))
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM50067033((2E,6E)-2,6-bis(4-hydroxy-3-methoxybenzylidene)cyc...)
Affinity DataIC50:  3.60E+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 PCBioAssay
TargetNuclear factor NF-kappa-B p105 subunit(Homo sapiens (Human))
Stc.Unm

US Patent
LigandPNGBDBM50067033((2E,6E)-2,6-bis(4-hydroxy-3-methoxybenzylidene)cyc...)
Affinity DataIC50:  4.20E+3nMAssay Description:TRAP Assay: The first procedure called for antioxidant activity to be measured as the ability of the analogs to react with the pre-formed radical mon...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetTissue factor(Homo sapiens (Human))TBA
LigandPNGBDBM50067033((2E,6E)-2,6-bis(4-hydroxy-3-methoxybenzylidene)cyc...)
Affinity DataIC50: >200nMAssay Description:Inhibition of tissue factor in Homo sapiens (human) THP1-cells using factor 10a chromogenic substrate assessed as inhibition of LPS-iduced procoagula...More data for this Ligand-Target Pair
In DepthDetails Article
TargetNuclear factor NF-kappa-B p105 subunit(Homo sapiens (Human))
Stc.Unm

US Patent
LigandPNGBDBM50067033((2E,6E)-2,6-bis(4-hydroxy-3-methoxybenzylidene)cyc...)
Affinity DataIC50:  4.40E+3nMAssay Description:The 293T/NF-κB-luc cells were re-plated 24 hr prior to treatment, into 24-well cell culture plates in media without hygromycin, to prevent it from...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetHistone acetyltransferase p300(Homo sapiens (Human))
Sapienza University Of Rome

Curated by ChEMBL
LigandPNGBDBM50067033((2E,6E)-2,6-bis(4-hydroxy-3-methoxybenzylidene)cyc...)
Affinity DataIC50:  1.11E+5nMAssay Description:Inhibition of GST-p300 HAT assessed as histone acetylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrase(Human immunodeficiency virus 1)
Sapienza University Of Rome

Curated by ChEMBL
LigandPNGBDBM50067033((2E,6E)-2,6-bis(4-hydroxy-3-methoxybenzylidene)cyc...)
Affinity DataIC50: >1.00E+5nMAssay Description:Compound concentration required to reduce HIV-1 Integrase 3'-processing activity by 50%More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrase(Human immunodeficiency virus 1)
Sapienza University Of Rome

Curated by ChEMBL
LigandPNGBDBM50067033((2E,6E)-2,6-bis(4-hydroxy-3-methoxybenzylidene)cyc...)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibitory activity against HIV-1 Integrase (HIV-1-IN)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTranscription factor Jun(Homo sapiens (Human))
Stc.Unm

US Patent
LigandPNGBDBM50067033((2E,6E)-2,6-bis(4-hydroxy-3-methoxybenzylidene)cyc...)
Affinity DataIC50:  7.30E+3nMAssay Description:TRAP Assay: The first procedure called for antioxidant activity to be measured as the ability of the analogs to react with the pre-formed radical mon...More data for this Ligand-Target Pair
In DepthDetails US Patent