BDBM50311741 1,6-dihydroxy-7-methoxy-8-(3-methylbut-2-enyl)-6',6'-dimethylpyrano(2',3':3,2)xanthone::9-hydroxycalabaxanthone::CHEMBL561643::mangostanin

SMILES [#6]-[#8]-c1c(-[#8])cc2oc3cc4-[#8]C([#6])([#6])[#6]=[#6]-c4c(-[#8])c3c(=O)c2c1-[#6]\[#6]=[#6](\[#6])-[#6]

InChI Key InChIKey=HQWHKELJHUFLGD-UHFFFAOYSA-N

Data  1 KI  7 IC50

  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 8 hits for monomerid = 50311741   

TargetSialidase(Clostridium perfringens)
Graduate School Of Gyeongsang National University

Curated by ChEMBL
LigandPNGBDBM50311741(1,6-dihydroxy-7-methoxy-8-(3-methylbut-2-enyl)-6',...)
Affinity DataKi:  5.90E+3nMAssay Description:Competitive inhibition of Clostridium perfringens neuraminidase by fluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNuclear factor NF-kappa-B p105 subunit(Homo sapiens (Human))
The Ohio State University

Curated by ChEMBL
LigandPNGBDBM50311741(1,6-dihydroxy-7-methoxy-8-(3-methylbut-2-enyl)-6',...)
Affinity DataIC50: >2.00E+4nMAssay Description:Inhibition of p50 after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTranscription factor p65(Homo sapiens (Human))
The Ohio State University

Curated by ChEMBL
LigandPNGBDBM50311741(1,6-dihydroxy-7-methoxy-8-(3-methylbut-2-enyl)-6',...)
Affinity DataIC50: >2.00E+4nMAssay Description:Inhibition of nuclear factor NF-kappa-B p65 subunit after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4D(Homo sapiens (Human))
Hainan University

Curated by ChEMBL
LigandPNGBDBM50311741(1,6-dihydroxy-7-methoxy-8-(3-methylbut-2-enyl)-6',...)
Affinity DataIC50:  420nMAssay Description:Inhibition of PDE4D2 (86-413) (unknown origin) expressed in Escherichia coli BL21 assessed as using [3H]-cAMP as substrate measured for 15 mins by li...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProbable maltase-glucoamylase 2(Homo sapiens)
University Of Wollongong

Curated by ChEMBL
LigandPNGBDBM50311741(1,6-dihydroxy-7-methoxy-8-(3-methylbut-2-enyl)-6',...)
Affinity DataIC50:  1.14E+4nMAssay Description:Inhibition of alpha-glucosidase (unknown origin) using p-nitrophenyl alpha-D-glucoside as substrate preincubated for 0.5 hrs followed substrate addit...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4D(Homo sapiens (Human))
Hainan University

Curated by ChEMBL
LigandPNGBDBM50311741(1,6-dihydroxy-7-methoxy-8-(3-methylbut-2-enyl)-6',...)
Affinity DataIC50:  420nMAssay Description:Inhibition of human PDE4D2 (86 to 413 residues) expressed in Escherichia coli BL21 codon-plus cells using [3H]cAMP as substrate incubated for 15 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty acid synthase(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50311741(1,6-dihydroxy-7-methoxy-8-(3-methylbut-2-enyl)-6',...)
Affinity DataIC50:  4.06E+4nMAssay Description:Inhibition of FASMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSialidase(Clostridium perfringens)
Graduate School Of Gyeongsang National University

Curated by ChEMBL
LigandPNGBDBM50311741(1,6-dihydroxy-7-methoxy-8-(3-methylbut-2-enyl)-6',...)
Affinity DataIC50:  2.01E+4nMAssay Description:Inhibition of Clostridium perfringens neuraminidase by fluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed