BDBM50241453 1,3,6,7-tetrahydroxy-2,8-bis(3-methylbut-2-enyl)-9H-xanthen-9-one::CHEMBL260553::gamma-mangostin

SMILES [#6]\[#6](-[#6])=[#6]\[#6]-c1c(-[#8])cc2oc3cc(-[#8])c(-[#8])c(-[#6]\[#6]=[#6](\[#6])-[#6])c3c(=O)c2c1-[#8]

InChI Key InChIKey=QAMMQIIXTAQRHX-UHFFFAOYSA-N

Data  4 KI  12 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 16 hits for monomerid = 50241453   

TargetFatty acid synthase(Human)
Chinese Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50241453(gamma-mangostin | 1,3,6,7-tetrahydroxy-2,8-bis(3-m...)
Affinity DataIC50: 1.24E+3nMAssay Description:Inhibition of FASMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAromatase(Human)
University of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50241453(gamma-mangostin | 1,3,6,7-tetrahydroxy-2,8-bis(3-m...)
Affinity DataIC50: 4.97E+3nMAssay Description:Inhibition of aromatase over-expressed in human SKBR3 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAromatase(Human)
University of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50241453(gamma-mangostin | 1,3,6,7-tetrahydroxy-2,8-bis(3-m...)
Affinity DataIC50: 6.90E+3nMAssay Description:Inhibition of aromatase in human placental microsomesMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSialidase(Clostridium perfringens)
Graduate School of Gyeongsang National University

Curated by ChEMBL
LigandPNGBDBM50241453(gamma-mangostin | 1,3,6,7-tetrahydroxy-2,8-bis(3-m...)
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of Clostridium perfringens neuraminidase by fluorimetryMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProstaglandin G/H synthase 1(Human)
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50241453(gamma-mangostin | 1,3,6,7-tetrahydroxy-2,8-bis(3-m...)
Affinity DataIC50: 800nMAssay Description:Inhibition of COX1More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProstaglandin G/H synthase 2(Human)
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50241453(gamma-mangostin | 1,3,6,7-tetrahydroxy-2,8-bis(3-m...)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of COX2More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProbable maltase-glucoamylase 2(Human)
Gyeongsang National University

Curated by ChEMBL
LigandPNGBDBM50241453(gamma-mangostin | 1,3,6,7-tetrahydroxy-2,8-bis(3-m...)
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of alpha-glucosidase (unknown origin) using PNP-G as substrate measured for 15 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Gyeongsang National University

Curated by ChEMBL
LigandPNGBDBM50241453(gamma-mangostin | 1,3,6,7-tetrahydroxy-2,8-bis(3-m...)
Affinity DataIC50: 2.80E+3nMAssay Description:Inhibition of recombinant human PTP1B (1 to 322 residues) expressed in Escherichia coli using P-NPP as substrate after 10 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetOxidized purine nucleoside triphosphate hydrolase(Human)
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50241453(gamma-mangostin | 1,3,6,7-tetrahydroxy-2,8-bis(3-m...)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of recombinant C-terminal 6xHis-tagged MTH1 (3 to 156 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) cells using dGTP ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPhosphoglycerate mutase 1(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50241453(gamma-mangostin | 1,3,6,7-tetrahydroxy-2,8-bis(3-m...)
Affinity DataIC50: 1.90E+3nMAssay Description:Inhibition of PGAM1 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetTransthyretin(Human)
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50241453(gamma-mangostin | 1,3,6,7-tetrahydroxy-2,8-bis(3-m...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of acid-mediated aggregation of TTR V30M mutant (unknown origin) expressed in Escherichia coli pretreated for 30 mins at pH 7 followed by ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetNAD-dependent protein deacetylase sirtuin-2(Human)
Minia University

Curated by ChEMBL
LigandPNGBDBM50241453(gamma-mangostin | 1,3,6,7-tetrahydroxy-2,8-bis(3-m...)
Affinity DataIC50: 3.80E+3nMAssay Description:Inhibition of human SIRT2 using sirtuin substrate incubated for 30 mins by enzymatic fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetSialidase(Clostridium perfringens)
Graduate School of Gyeongsang National University

Curated by ChEMBL
LigandPNGBDBM50241453(gamma-mangostin | 1,3,6,7-tetrahydroxy-2,8-bis(3-m...)
Affinity DataKi:  800nMAssay Description:Competitive inhibition of Clostridium perfringens neuraminidase by fluorimetryMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProbable maltase-glucoamylase 2(Human)
Gyeongsang National University

Curated by ChEMBL
LigandPNGBDBM50241453(gamma-mangostin | 1,3,6,7-tetrahydroxy-2,8-bis(3-m...)
Affinity DataKi:  1.40E+3nMAssay Description:Inhibition of alpha-glucosidase (unknown origin) using PNP-G as substrate by Dixon plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Gyeongsang National University

Curated by ChEMBL
LigandPNGBDBM50241453(gamma-mangostin | 1,3,6,7-tetrahydroxy-2,8-bis(3-m...)
Affinity DataKi:  2.70E+3nMAssay Description:Inhibition of recombinant human PTP1B (1 to 322 residues) expressed in Escherichia coli using P-NPP as substrate after 10 mins by Dixon plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetIsocitrate dehydrogenase [NADP] cytoplasmic(Human)
Dongguk University

Curated by ChEMBL
LigandPNGBDBM50241453(gamma-mangostin | 1,3,6,7-tetrahydroxy-2,8-bis(3-m...)
Affinity DataKi:  3.17E+3nMAssay Description:Competitive inhibition of IDH1-R132H mutant (unknown origin) using a-ketoglutarate and NADPH as substrate by steady state kinetic analysisMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed