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Found 68 with Last Name = 'maiti' and Initial = 'a'
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM29227(casimiroin analogue, 1p)
Affinity DataIC50:  100nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM9460(3-(4-aminophenyl)-3-ethyl-piperidine-2,6-dione | 3...)
Affinity DataIC50:  270nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM9460(3-(4-aminophenyl)-3-ethyl-piperidine-2,6-dione | 3...)
Affinity DataIC50:  270nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM29229(casimiroin analogue, 1r)
Affinity DataIC50:  760nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM29221(casimiroin analogue, 1j)
Affinity DataIC50:  960nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM23926((E)-resveratrol | 5-[(E)-2-(4-hydroxyphenyl)etheny...)
Affinity DataIC50:  960nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM29223(casimiroin analogue, 1l)
Affinity DataIC50:  960nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM29213(casimiroin analogue, 1b)
Affinity DataIC50:  1.25E+3nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM50213235((+/-)-7-methoxy-2-(4-methoxyphenyl)chroman-4-one |...)
Affinity DataIC50:  1.86E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM29221(casimiroin analogue, 1j)
Affinity DataIC50:  1.90E+3nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM29217(casimiroin analogue, 1f)
Affinity DataIC50:  2.02E+3nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM29225(casimiroin analogue, 1n)
Affinity DataIC50:  2.72E+3nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOrnithine decarboxylase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50202558(5,6,2',6'-tetramethoxyflavone | CHEMBL375582)
Affinity DataIC50:  3.40E+3nMAssay Description:Inhibition of TPA-induced ODC activity in T24 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM50213245(7-methoxy-2-[4-methoxy-3-(3-methylbut-2-enyl)pheny...)
Affinity DataIC50:  3.67E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM29210(casimiroin)
Affinity DataIC50:  3.92E+3nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM50213239(7-Hydroxy-2-[4'-methoxy-3'-(3-methylbut-2-enyl)phe...)
Affinity DataIC50:  4.08E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM29223(casimiroin analogue, 1l)
Affinity DataIC50:  4.10E+3nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM50213241(7-methoxy-2-[3-(3-methylbut-2-enyl)phenyl]chroman-...)
Affinity DataIC50:  4.67E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM50213236(2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-7-metho...)
Affinity DataIC50:  4.75E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM29228(casimiroin analogue, 1q)
Affinity DataIC50:  5.68E+3nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM29219(casimiroin analogue, 1h)
Affinity DataIC50:  5.76E+3nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM29217(casimiroin analogue, 1f)
Affinity DataIC50:  5.80E+3nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM29226(casimiroin analogue, 1o)
Affinity DataIC50:  6.00E+3nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM29213(casimiroin analogue, 1b)
Affinity DataIC50:  6.20E+3nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM29225(casimiroin analogue, 1n)
Affinity DataIC50:  7.00E+3nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM50213252(2-[4-methoxy-3-(3-methylbut-2-enyl)phenyl]-7-(meth...)
Affinity DataIC50:  7.67E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM29220(casimiroin analogue, 1i)
Affinity DataIC50:  8.80E+3nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM29219(casimiroin analogue, 1h)
Affinity DataIC50:  9.30E+3nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM29224(casimiroin analogue, 1m)
Affinity DataIC50:  1.00E+4nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM29227(casimiroin analogue, 1p)
Affinity DataIC50:  1.08E+4nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM29222(casimiroin analogue, 1k)
Affinity DataIC50:  1.08E+4nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM29212(casimiroin analogue, 1a)
Affinity DataIC50:  1.08E+4nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM9019(CHEMBL45 | Melatonin | N-[2-(5-methoxy-1H-indol-3-...)
Affinity DataIC50:  1.13E+4nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM50370985(CHEMBL1162951)
Affinity DataIC50:  1.21E+4nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM50213234(7-(methoxymethoxy)-2-[4-(methoxymethoxy)-3-(3-meth...)
Affinity DataIC50:  1.40E+4nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM29226(casimiroin analogue, 1o)
Affinity DataIC50:  1.48E+4nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM29215(casimiroin analogue, 1d)
Affinity DataIC50:  1.82E+4nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM29224(casimiroin analogue, 1m)
Affinity DataIC50:  1.85E+4nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM29216(casimiroin analogue, 1e)
Affinity DataIC50:  2.41E+4nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM50213243(7-methoxy-2-[4-(methoxymethoxy)-3-(3-methylbut-2-e...)
Affinity DataIC50:  2.51E+4nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM29222(casimiroin analogue, 1k)
Affinity DataIC50:  2.68E+4nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM50213238(7-methoxy-2-[4-(3-methylbut-2-enyloxy)phenyl]chrom...)
Affinity DataIC50:  2.87E+4nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM29218(casimiroin analogue, 1g)
Affinity DataIC50:  2.93E+4nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM29218(casimiroin analogue, 1g)
Affinity DataIC50:  3.15E+4nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM50213251((rac)-7-hydroxy-2-(4-hydroxy-3-(3-methylbut-2-enyl...)
Affinity DataIC50:  4.10E+4nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRibosyldihydronicotinamide dehydrogenase [quinone](Homo sapiens (Human))
Purdue University

LigandPNGBDBM29210(casimiroin)
Affinity DataIC50:  5.41E+4nMpH: 7.5 T: 2°CAssay Description:The activity of QR2 under steady-state conditions was evaluated on SpectraMax Plus 384 UV/vis spectrophotometer by monitoring the increase in absorba...More data for this Ligand-Target Pair
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM50213248(3-hydroxy-1-(2-hydroxy-4-methoxyphenyl)-3-[4-metho...)
Affinity DataIC50:  5.47E+4nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM50213240(1-(2,4-Dihydroxyphenyl)-3-[4-methoxy-3-(3-methylbu...)
Affinity DataIC50:  8.29E+4nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM29220(casimiroin analogue, 1i)
Affinity DataIC50: >9.13E+4nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

LigandPNGBDBM29230(quinone, 12)
Affinity DataIC50: >9.84E+4nMAssay Description:Aromatase inhibition was quantified by measuring the fluorescent intensity of fluorescein, the hydrolysis product of dibenzylfluorescein (DBF), by ar...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
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