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Found 38 with Last Name = 'mahidol' and Initial = 'c'
TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM13061(4,4 -(1H-1,2,4-triazol-1-ylmethanediyl)dibenzonitr...)
Affinity DataIC50:  1nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM50398447(Aromasin | EXEMESTANE)
Affinity DataIC50:  23nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM31768(CHEMBL295698 | Ketoconazole | Nizoral | Panfungol)
Affinity DataIC50:  2.40E+3nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM8610(1-[4-(4-{[(2R,4S)-2-(2,4-dichlorophenyl)-2-(1H-imi...)
Affinity DataIC50:  2.40E+3nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Chulabhorn Research Institute

Curated by ChEMBL
LigandPNGBDBM35440(ALLOPURINOL | MLS000069453 | SMR000059083 | cid_20...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibition of xanthine oxidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM50576415(CHEMBL4852023)
Affinity DataIC50:  3.70E+3nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Chiang Mai University

Curated by ChEMBL
LigandPNGBDBM50211965(5,6-dihydro-3,7-dihydroxy-1,4-methoxy-2-methyldibe...)
Affinity DataIC50:  6.90E+3nMAssay Description:Inhibition of COX2 by radioimmunoassay methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM50576410(CHEMBL4875917)
Affinity DataIC50:  7.20E+3nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM50576414(CHEMBL4874928)
Affinity DataIC50:  7.90E+3nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Chiang Mai University

Curated by ChEMBL
LigandPNGBDBM50211952(5,6-dihydro-8-hydroxy-3-methoxy-1,4-dione-2-methyl...)
Affinity DataIC50:  1.01E+4nMAssay Description:Inhibition of COX2 by radioimmunoassay methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM50576413(CHEMBL4863718)
Affinity DataIC50:  1.04E+4nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM50576412(CHEMBL4859743)
Affinity DataIC50:  1.07E+4nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Chiang Mai University

Curated by ChEMBL
LigandPNGBDBM22360(2-(acetyloxy)benzoate | 2-(acetyloxy)benzoic acid ...)
Affinity DataIC50:  1.14E+4nMAssay Description:Inhibition of COX1 by radioimmunoassay methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM50576411(CHEMBL4866633)
Affinity DataIC50:  1.18E+4nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM50335903((3R,4R)-4,8-dihydroxy-3-((R)-2-hydroxypentyl)-6,7-...)
Affinity DataIC50: >1.53E+4nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM50335901(CHEMBL1668327 | fusarentin 6,7-dimethylether)
Affinity DataIC50: >1.61E+4nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM50335904(CHEMBL1668329 | Colletotrialide)
Affinity DataIC50: >1.62E+4nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM50335899(CHEMBL488513 | monocerin)
Affinity DataIC50: >1.62E+4nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM50335902(CHEMBL1668328 | fusarentin 6-methyl ether)
Affinity DataIC50: >1.68E+4nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM50335900((2S,3aR,9bR)-6,7-dihydroxy-8-methoxy-2-propyl-3,3a...)
Affinity DataIC50: >1.69E+4nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Chiang Mai University

Curated by ChEMBL
LigandPNGBDBM22360(2-(acetyloxy)benzoate | 2-(acetyloxy)benzoic acid ...)
Affinity DataIC50:  1.98E+4nMAssay Description:Inhibition of COX2 by radioimmunoassay methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Chiang Mai University

Curated by ChEMBL
LigandPNGBDBM50211951(5,6-dihydro-4,7-dihydroxy-1,3-methoxy-2-methyldibe...)
Affinity DataIC50: >3.31E+4nMAssay Description:Inhibition of COX2 by radioimmunoassay methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Chiang Mai University

Curated by ChEMBL
LigandPNGBDBM50211951(5,6-dihydro-4,7-dihydroxy-1,3-methoxy-2-methyldibe...)
Affinity DataIC50: >3.31E+4nMAssay Description:Inhibition of COX1 by radioimmunoassay methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Chiang Mai University

Curated by ChEMBL
LigandPNGBDBM50211965(5,6-dihydro-3,7-dihydroxy-1,4-methoxy-2-methyldibe...)
Affinity DataIC50: >3.31E+4nMAssay Description:Inhibition of COX1 by radioimmunoassay methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Chiang Mai University

Curated by ChEMBL
LigandPNGBDBM50211958(5,6-dihydro-7-hydroxy-3-methoxy-1,4-dione-2-methyl...)
Affinity DataIC50: >3.49E+4nMAssay Description:Inhibition of COX1 by radioimmunoassay methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Chiang Mai University

Curated by ChEMBL
LigandPNGBDBM50211952(5,6-dihydro-8-hydroxy-3-methoxy-1,4-dione-2-methyl...)
Affinity DataIC50: >3.49E+4nMAssay Description:Inhibition of COX1 by radioimmunoassay methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Chiang Mai University

Curated by ChEMBL
LigandPNGBDBM50211958(5,6-dihydro-7-hydroxy-3-methoxy-1,4-dione-2-methyl...)
Affinity DataIC50: >3.49E+4nMAssay Description:Inhibition of COX2 by radioimmunoassay methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Chiang Mai University

Curated by ChEMBL
LigandPNGBDBM50211956(2-(3-hydroxy-5-methoxyphenethyl)phenol | Batatasin...)
Affinity DataIC50: >4.09E+4nMAssay Description:Inhibition of COX2 by radioimmunoassay methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Chiang Mai University

Curated by ChEMBL
LigandPNGBDBM50211956(2-(3-hydroxy-5-methoxyphenethyl)phenol | Batatasin...)
Affinity DataIC50: >4.09E+4nMAssay Description:Inhibition of COX1 by radioimmunoassay methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Chiang Mai University

Curated by ChEMBL
LigandPNGBDBM50211960(3,5-Dihydroxybibenzyl | 5-phenethylbenzene-1,3-dio...)
Affinity DataIC50: >4.67E+4nMAssay Description:Inhibition of COX1 by radioimmunoassay methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Chiang Mai University

Curated by ChEMBL
LigandPNGBDBM50211960(3,5-Dihydroxybibenzyl | 5-phenethylbenzene-1,3-dio...)
Affinity DataIC50: >4.67E+4nMAssay Description:Inhibition of COX2 by radioimmunoassay methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Chulabhorn Royal Academy

Curated by ChEMBL
LigandPNGBDBM50311536(Aspergillusol A | CHEMBL1088570)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Chulabhorn Research Institute

Curated by ChEMBL
LigandPNGBDBM50335903((3R,4R)-4,8-dihydroxy-3-((R)-2-hydroxypentyl)-6,7-...)
Affinity DataIC50: >6.12E+5nMAssay Description:Inhibition of Xanthine oxidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Chulabhorn Research Institute

Curated by ChEMBL
LigandPNGBDBM50335901(CHEMBL1668327 | fusarentin 6,7-dimethylether)
Affinity DataIC50: >6.44E+5nMAssay Description:Inhibition of Xanthine oxidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Chulabhorn Research Institute

Curated by ChEMBL
LigandPNGBDBM50335899(CHEMBL488513 | monocerin)
Affinity DataIC50: >6.48E+5nMAssay Description:Inhibition of Xanthine oxidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Chulabhorn Research Institute

Curated by ChEMBL
LigandPNGBDBM50335904(CHEMBL1668329 | Colletotrialide)
Affinity DataIC50: >6.48E+5nMAssay Description:Inhibition of Xanthine oxidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Chulabhorn Research Institute

Curated by ChEMBL
LigandPNGBDBM50335902(CHEMBL1668328 | fusarentin 6-methyl ether)
Affinity DataIC50: >6.75E+5nMAssay Description:Inhibition of Xanthine oxidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Chulabhorn Research Institute

Curated by ChEMBL
LigandPNGBDBM50335900((2S,3aR,9bR)-6,7-dihydroxy-8-methoxy-2-propyl-3,3a...)
Affinity DataIC50: >6.79E+5nMAssay Description:Inhibition of Xanthine oxidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed