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Found 1121 with Last Name = 'park' and Initial = 'ej'
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM13061(4,4 -(1H-1,2,4-triazol-1-ylmethanediyl)dibenzonitr...)
Affinity DataKi:  0.0200nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)
Affinity DataKi:  0.0500nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366125(CHEMBL1957214)
Affinity DataKi:  0.0600nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM10015(2-[3-(1-cyano-1-methylethyl)-5-(1H-1,2,4-triazol-1...)
Affinity DataKi:  0.130nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366128(CHEMBL1957217)
Affinity DataKi:  0.650nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Green Cross

Curated by ChEMBL
LigandPNGBDBM50130293(7-{4-[4-(2,3-dichlorophenyl)piperazin-1-yl]butoxy}...)
Affinity DataKi:  0.800nMAssay Description:Binding affinity to 5-HT2AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Green Cross

Curated by ChEMBL
LigandPNGBDBM50313283(1-{2-[4-(6-Fluoro-1H-indol-3-yl)-3,6-dihydro-2H-py...)
Affinity DataKi:  0.810nMAssay Description:Inhibition of 5-HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Green Cross

Curated by ChEMBL
LigandPNGBDBM50313283(1-{2-[4-(6-Fluoro-1H-indol-3-yl)-3,6-dihydro-2H-py...)
Affinity DataKi:  0.810nMAssay Description:Binding affinity to 5-HT2AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Green Cross

Curated by ChEMBL
LigandPNGBDBM50313283(1-{2-[4-(6-Fluoro-1H-indol-3-yl)-3,6-dihydro-2H-py...)
Affinity DataKi:  2.30nMAssay Description:Binding affinity to SERTMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Green Cross

Curated by ChEMBL
LigandPNGBDBM50313283(1-{2-[4-(6-Fluoro-1H-indol-3-yl)-3,6-dihydro-2H-py...)
Affinity DataKi:  2.30nMAssay Description:Inhibition of SERTMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366129(CHEMBL1957218)
Affinity DataKi:  3.20nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Green Cross

Curated by ChEMBL
LigandPNGBDBM50069447(1-(3-(4-(m-Chlorophenyl)-1-piperazinyl)propyl)-3-e...)
Affinity DataKi:  5.80nMAssay Description:Binding affinity to 5-HT2AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366127(CHEMBL1957216)
Affinity DataKi:  8.20nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Green Cross

Curated by ChEMBL
LigandPNGBDBM50313284((S)-2-((7-fluoro-2,3-dihydro-1H-inden-4-yloxy)meth...)
Affinity DataKi:  21nMAssay Description:Inhibition of SERTMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Green Cross

Curated by ChEMBL
LigandPNGBDBM50313284((S)-2-((7-fluoro-2,3-dihydro-1H-inden-4-yloxy)meth...)
Affinity DataKi:  21nMAssay Description:Binding affinity to SERTMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366134(CHEMBL1957223)
Affinity DataKi:  35nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366120(CHEMBL1601919)
Affinity DataKi:  63nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366132(CHEMBL1957221)
Affinity DataKi:  83nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Green Cross

Curated by ChEMBL
LigandPNGBDBM50313284((S)-2-((7-fluoro-2,3-dihydro-1H-inden-4-yloxy)meth...)
Affinity DataKi:  86nMAssay Description:Inhibition of 5-HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Green Cross

Curated by ChEMBL
LigandPNGBDBM50313284((S)-2-((7-fluoro-2,3-dihydro-1H-inden-4-yloxy)meth...)
Affinity DataKi:  86nMAssay Description:Binding affinity to 5-HT2AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Green Cross

Curated by ChEMBL
LigandPNGBDBM50130293(7-{4-[4-(2,3-dichlorophenyl)piperazin-1-yl]butoxy}...)
Affinity DataKi:  98nMAssay Description:Binding affinity to SERTMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366133(CHEMBL1957222)
Affinity DataKi:  100nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366122(CHEMBL1957211)
Affinity DataKi:  234nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366130(CHEMBL1957219)
Affinity DataKi:  285nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent serotonin transporter(Homo sapiens (Human))
Green Cross

Curated by ChEMBL
LigandPNGBDBM50069447(1-(3-(4-(m-Chlorophenyl)-1-piperazinyl)propyl)-3-e...)
Affinity DataKi:  290nMAssay Description:Binding affinity to SERTMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366118(CHEMBL1957208)
Affinity DataKi:  1.16E+3nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366131(CHEMBL1957220)
Affinity DataKi:  1.48E+3nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAnthranilate phosphoribosyltransferase(Mycobacterium tuberculosis)
University of Auckland

LigandPNGBDBM93073(ACS No 172)
Affinity DataKi:  1.50E+3nMAssay Description:The initial screen was performed in a 96-well plate using the fluoresence-based assay previously described. An enzyme-coupled absorbance-based assay...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366123(CHEMBL1957212)
Affinity DataKi:  1.72E+3nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366126(CHEMBL1957215)
Affinity DataKi:  2.55E+3nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospho-2-dehydro-3-deoxyheptonate aldolase, Phe-sensitive(Escherichia coli (strain K12))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50350727(CHEMBL1818159)
Affinity DataKi:  3.60E+3nMAssay Description:Competitive inhibition of recombinant Escherichia coli DAH7P synthase using PEP as substrate by Michaelis-Menten equation analysis using UV-visible s...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospho-2-dehydro-3-deoxyheptonate aldolase, Phe-sensitive(Escherichia coli (strain K12))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50350723(CHEMBL1255768 | CHEMBL1818156)
Affinity DataKi:  4.70E+3nMAssay Description:Inhibition of recombinant Escherichia coli DAH7P synthaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospho-2-dehydro-3-deoxyheptonate aldolase, Phe-sensitive(Escherichia coli (strain K12))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50350725(CHEMBL1818157 | CHEMBL1818158)
Affinity DataKi:  5.30E+3nMAssay Description:Competitive inhibition of recombinant Escherichia coli DAH7P synthase using PEP as substrate by Michaelis-Menten equation analysis using UV-visible s...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366119(CHEMBL1957209)
Affinity DataKi:  5.32E+3nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAnthranilate phosphoribosyltransferase(Mycobacterium tuberculosis)
University of Auckland

LigandPNGBDBM93074(ACS No 142)
Affinity DataKi:  6.30E+3nMAssay Description:The initial screen was performed in a 96-well plate using the fluoresence-based assay previously described. An enzyme-coupled absorbance-based assay...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target2-dehydro-3-deoxyphosphooctonate aldolase(Neisseria meningitidis serogroup B (strain MC58))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50362546(CHEMBL1938424)
Affinity DataKi:  7.90E+3nMAssay Description:Competitive inhibition of Neisseria meningitidis serotype B strain MC58 ATCC BAA355 KDO8P synthase expressed in Escherichia coli BL21 (DE3) cells usi...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366121(CHEMBL1957210)
Affinity DataKi:  1.26E+4nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50366124(CHEMBL1957213)
Affinity DataKi:  1.50E+4nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAnthranilate phosphoribosyltransferase(Mycobacterium tuberculosis)
University of Auckland

LigandPNGBDBM93075(ACS No 145)
Affinity DataKi:  1.50E+4nMAssay Description:The initial screen was performed in a 96-well plate using the fluoresence-based assay previously described. An enzyme-coupled absorbance-based assay...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAnthranilate phosphoribosyltransferase(Mycobacterium tuberculosis)
University of Auckland

LigandPNGBDBM93076(ACS No 174)
Affinity DataKi:  1.80E+4nMAssay Description:The initial screen was performed in a 96-well plate using the fluoresence-based assay previously described. An enzyme-coupled absorbance-based assay...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAnthranilate phosphoribosyltransferase(Mycobacterium tuberculosis)
University of Auckland

LigandPNGBDBM93077(ACS No 179)
Affinity DataKi:  1.90E+4nMAssay Description:The initial screen was performed in a 96-well plate using the fluoresence-based assay previously described. An enzyme-coupled absorbance-based assay...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM23926((E)-resveratrol | 5-[(E)-2-(4-hydroxyphenyl)etheny...)
Affinity DataKi:  4.17E+4nMAssay Description:Competitive inhibition of human aromatase using dibenzylfluorescein substrate after 10 mins preincubation measured every 10 sec for 5 mins by Michael...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAnthranilate phosphoribosyltransferase(Mycobacterium tuberculosis)
University of Auckland

LigandPNGBDBM93078(ACS No 126)
Affinity DataKi:  6.00E+4nMAssay Description:The initial screen was performed in a 96-well plate using the fluoresence-based assay previously described. An enzyme-coupled absorbance-based assay...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAnthranilate phosphoribosyltransferase(Mycobacterium tuberculosis)
University of Auckland

LigandPNGBDBM93079(ACS No 165)
Affinity DataKi:  7.90E+4nMAssay Description:The initial screen was performed in a 96-well plate using the fluoresence-based assay previously described. An enzyme-coupled absorbance-based assay...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAnthranilate phosphoribosyltransferase(Mycobacterium tuberculosis)
University of Auckland

LigandPNGBDBM85513(ACS No 10 | CAS_54-21-7 | NSC_5900 | Sodium salicy...)
Affinity DataKi:  1.19E+5nMAssay Description:The initial screen was performed in a 96-well plate using the fluoresence-based assay previously described. An enzyme-coupled absorbance-based assay...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospho-2-dehydro-3-deoxyheptonate aldolase, Phe-sensitive(Escherichia coli (strain K12))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50350725(CHEMBL1818157 | CHEMBL1818158)
Affinity DataKi:  1.54E+5nMAssay Description:Competitive inhibition of recombinant Escherichia coli DAH7P synthase using PEP as substrate by Michaelis-Menten equation analysis using UV-visible s...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target2-dehydro-3-deoxyphosphooctonate aldolase(Neisseria meningitidis serogroup B (strain MC58))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50281349(CHEMBL95764 | N-(phosphonomethyl)glycine | glyphos...)
Affinity DataKi:  2.60E+5nMAssay Description:Competitive inhibition of Neisseria meningitidis serotype B strain MC58 ATCC BAA355 KDO8P synthase expressed in Escherichia coli BL21 (DE3) cells usi...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhospho-2-dehydro-3-deoxyheptonate aldolase, Phe-sensitive(Escherichia coli (strain K12))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50350723(CHEMBL1255768 | CHEMBL1818156)
Affinity DataKi:  2.70E+5nMAssay Description:Inhibition of recombinant Escherichia coli DAH7P synthaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target2-dehydro-3-deoxyphosphooctonate aldolase(Neisseria meningitidis serogroup B (strain MC58))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50362548(CHEMBL1941140)
Affinity DataKi:  2.70E+5nMAssay Description:Competitive inhibition of Neisseria meningitidis serotype B strain MC58 ATCC BAA355 KDO8P synthase expressed in Escherichia coli BL21 (DE3) cells usi...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target2-dehydro-3-deoxyphosphooctonate aldolase(Neisseria meningitidis serogroup B (strain MC58))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50362544(CHEMBL1941138)
Affinity DataKi:  8.70E+5nMAssay Description:Competitive inhibition of Neisseria meningitidis serotype B strain MC58 ATCC BAA355 KDO8P synthase expressed in Escherichia coli BL21 (DE3) cells usi...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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