null

SMILES Oc1cc2oc(c(O)cc2c(=[OH+])c1)-c1cc(O)c(O)c(O)c1

InChI Key InChIKey=ZSNRRIMMZSGWJW-UHFFFAOYSA-O

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 7 hits for monomerid = 50326997   

TargetLactoylglutathione lyase(Homo sapiens (Human))
Tokyo University of Science

Curated by ChEMBL
LigandPNGBDBM50326997(CHEMBL590878 | Delphinidin)copy SMILEScopy InChI
Affinity DataIC50: 1.90E+3nMAssay Description:Inhibition of human recombinant glyoxalase 1 assessed as S-D-lactoylglutathione after 15 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC32K6PubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
UMR 7200 CNRS-Universit£ de Strasbourg

Curated by ChEMBL
LigandPNGBDBM50326997(CHEMBL590878 | Delphinidin)copy SMILEScopy InChI
Affinity DataIC50: 1.46E+4nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2WJXPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Cairo University

Curated by ChEMBL
LigandPNGBDBM50326997(CHEMBL590878 | Delphinidin)copy SMILEScopy InChI
Affinity DataIC50: 6.30nMAssay Description:Inhibition of EGFR (unknown origin) using poly (Glu, Tyr) 4:1 as substrate after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N25CVPubMed
TargetNAD-dependent protein deacylase sirtuin-6(Homo sapiens (Human))TBA
LigandPNGBDBM50326997(CHEMBL590878 | Delphinidin)copy SMILEScopy InChI
Affinity DataEC50:  7.60E+5nMAssay Description:Antagonist activity at histamine H3 receptor in electrically-stimulated guinea pig ileumMore data for this Ligand-Target Pair
In DepthDetails
TargetCREB-binding protein/Histone acetyltransferase p300(Homo sapiens (Human))
Sichuan University

Curated by ChEMBL
LigandPNGBDBM50326997(CHEMBL590878 | Delphinidin)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of p300 (unknown origin)/CBP (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1QC8PubMed
TargetAlpha-synuclein(Homo sapiens (Human))TBA
LigandPNGBDBM50326997(CHEMBL590878 | Delphinidin)copy SMILEScopy InChI
Affinity DataIC50: 6.50E+3nMAssay Description:Inhibition of human alpha-synuclein filament formation expressed in Escherichia coli BL21(DE3) cells incubated for 72 hrs by thioflavin S based fluor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H998V9PubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Cairo University

Curated by ChEMBL
LigandPNGBDBM50326997(CHEMBL590878 | Delphinidin)copy SMILEScopy InChI
Affinity DataIC50: 5.10nMAssay Description:Inhibition of VEGFR-2 (unknown origin) using poly (Glu, Tyr) 4:1 as substrate after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N25CVPubMed