Compile Data Set for Download or QSAR
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Found 552 with Last Name = 'hernandez' and Initial = 'v'
TargetP2X purinoceptor 4(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50370141(TNP-ATP)
Affinity DataKi:  49nMAssay Description:Competitive antagonist activity at human P2X4 receptor expressed in 1321N1 cell membrane assessed as inhibition of [35S]ATPgammaS binding by scintill...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066974(7-Benzyl-2,3-dihydroxy-6-methyl-4-propyl-naphthale...)
Affinity DataKi:  50nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066979(2,3-Dihydroxy-6,7-dimethyl-4-propyl-naphthalene-1-...)
Affinity DataKi:  100nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066979(2,3-Dihydroxy-6,7-dimethyl-4-propyl-naphthalene-1-...)
Affinity DataKi:  100nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066973(2,3-Dihydroxy-4-isopropyl-6-methyl-7-(4-trifluorom...)
Affinity DataKi:  200nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066975(7-Benzyl-2,3-dihydroxy-4-isopropyl-6-methyl-naphth...)
Affinity DataKi:  200nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066974(7-Benzyl-2,3-dihydroxy-6-methyl-4-propyl-naphthale...)
Affinity DataKi:  300nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066976(7-Benzyl-2,3-dihydroxy-4,6-dimethyl-naphthalene-1-...)
Affinity DataKi:  500nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066975(7-Benzyl-2,3-dihydroxy-4-isopropyl-6-methyl-naphth...)
Affinity DataKi:  700nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066974(7-Benzyl-2,3-dihydroxy-6-methyl-4-propyl-naphthale...)
Affinity DataKi:  1.00E+3nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066977(2,3-Dihydroxy-6-methyl-4-propyl-naphthalene-1-carb...)
Affinity DataKi:  1.00E+3nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066981(2,3-Dihydroxy-4-isopropyl-6,7-dimethyl-naphthalene...)
Affinity DataKi:  1.00E+3nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeucine--tRNA ligase, cytoplasmic(Saccharomyces cerevisiae S288c)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50370987(TAVABOROLE)
Affinity DataKi:  1.85E+3nMAssay Description:Inhibition of Saccharomyces cerevisiae cytoplasmic leucyl-tRNA synthetase after 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50031638(2,3-Dihydroxy-4-isopropyl-6-methyl-naphthalene-1-c...)
Affinity DataKi:  2.00E+3nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066981(2,3-Dihydroxy-4-isopropyl-6,7-dimethyl-naphthalene...)
Affinity DataKi:  2.00E+3nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50031638(2,3-Dihydroxy-4-isopropyl-6-methyl-naphthalene-1-c...)
Affinity DataKi:  3.00E+3nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066980(2,3-Dihydroxy-4,6,7-trimethyl-naphthalene-1-carbox...)
Affinity DataKi:  4.00E+3nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Goethe-University Frankfurt

Curated by ChEMBL
LigandPNGBDBM50530480(CHEMBL4445524)
Affinity DataKi:  4.80E+3nMAssay Description:Competitive inhibition of full length human soluble epoxide hydrolase pre-incubated for 30 mins before DiFMUP substrate addition by fluorescence base...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Goethe-University Frankfurt

Curated by ChEMBL
LigandPNGBDBM50530480(CHEMBL4445524)
Affinity DataKi:  4.80E+3nMAssay Description:Competitive inhibition of full length human soluble epoxide hydrolase pre-incubated for 30 mins before DiFMUP substrate addition by fluorescence base...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066977(2,3-Dihydroxy-6-methyl-4-propyl-naphthalene-1-carb...)
Affinity DataKi:  6.00E+3nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066975(7-Benzyl-2,3-dihydroxy-4-isopropyl-6-methyl-naphth...)
Affinity DataKi:  7.00E+3nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066976(7-Benzyl-2,3-dihydroxy-4,6-dimethyl-naphthalene-1-...)
Affinity DataKi:  8.00E+3nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066973(2,3-Dihydroxy-4-isopropyl-6-methyl-7-(4-trifluorom...)
Affinity DataKi:  1.30E+4nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066980(2,3-Dihydroxy-4,6,7-trimethyl-naphthalene-1-carbox...)
Affinity DataKi:  1.30E+4nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066979(2,3-Dihydroxy-6,7-dimethyl-4-propyl-naphthalene-1-...)
Affinity DataKi:  1.90E+4nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066978(2,3-Dihydroxy-4,6-dimethyl-naphthalene-1-carboxyli...)
Affinity DataKi:  2.20E+4nMAssay Description:inhibitory activity against P. falciparum lactate dehydrogenase (pLDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeucine--tRNA ligase, cytoplasmic(Saccharomyces cerevisiae S288c)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50370987(TAVABOROLE)
Affinity DataKi:  3.14E+4nMAssay Description:Inhibition of Saccharomyces cerevisiae cytoplasmic leucyl-tRNA synthetase after 2 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066978(2,3-Dihydroxy-4,6-dimethyl-naphthalene-1-carboxyli...)
Affinity DataKi:  3.40E+4nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066976(7-Benzyl-2,3-dihydroxy-4,6-dimethyl-naphthalene-1-...)
Affinity DataKi:  3.90E+4nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066977(2,3-Dihydroxy-6-methyl-4-propyl-naphthalene-1-carb...)
Affinity DataKi:  4.90E+4nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066981(2,3-Dihydroxy-4-isopropyl-6,7-dimethyl-naphthalene...)
Affinity DataKi:  7.80E+4nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066973(2,3-Dihydroxy-4-isopropyl-6-methyl-7-(4-trifluorom...)
Affinity DataKi:  8.10E+4nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50031638(2,3-Dihydroxy-4-isopropyl-6-methyl-naphthalene-1-c...)
Affinity DataKi:  9.10E+4nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066980(2,3-Dihydroxy-4,6,7-trimethyl-naphthalene-1-carbox...)
Affinity DataKi:  1.90E+5nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase B chain(Homo sapiens (Human))
University Of New Mexico School Of Medicine

Curated by ChEMBL
LigandPNGBDBM50066978(2,3-Dihydroxy-4,6-dimethyl-naphthalene-1-carboxyli...)
Affinity DataKi: >2.50E+5nMAssay Description:inhibitory activity against Human Lactate Dehydrogenase (LDH-H)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 2(Homo sapiens (Human))
Pharmbiotec

Curated by ChEMBL
LigandPNGBDBM50466033(CHEMBL4293115)
Affinity DataIC50:  0.320nMAssay Description:Inhibition of human placental microsomal fraction 17beta-HSD2 using [3H]-E2 as substrate after 20 mins in presence of NAD+ by radio-flow detector bas...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 1(Homo sapiens (Human))
Pharmbiotec

Curated by ChEMBL
LigandPNGBDBM50466018(CHEMBL4283851)
Affinity DataIC50:  0.400nMAssay Description:Inhibition of human placental cytosolic 17beta-HSD1 using [3H]-E1 as substrate after 10 mins in presence of NADPH by radio-flow detector based analys...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 2(Homo sapiens (Human))
Pharmbiotec

Curated by ChEMBL
LigandPNGBDBM50466021(CHEMBL4295076)
Affinity DataIC50:  0.630nMAssay Description:Inhibition of human placental microsomal fraction 17beta-HSD2 using [3H]-E2 as substrate after 20 mins in presence of NAD+ by radio-flow detector bas...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 2(Homo sapiens (Human))
Pharmbiotec

Curated by ChEMBL
LigandPNGBDBM50466032(CHEMBL4276934)
Affinity DataIC50:  0.850nMAssay Description:Inhibition of human placental microsomal fraction 17beta-HSD2 using [3H]-E2 as substrate after 20 mins in presence of NAD+ by radio-flow detector bas...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 1(Homo sapiens (Human))
Pharmbiotec

Curated by ChEMBL
LigandPNGBDBM50466019(CHEMBL4286251)
Affinity DataIC50:  0.900nMAssay Description:Inhibition of human placental cytosolic 17beta-HSD1 using [3H]-E1 as substrate after 10 mins in presence of NADPH by radio-flow detector based analys...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 2(Homo sapiens (Human))
Pharmbiotec

Curated by ChEMBL
LigandPNGBDBM50466034(CHEMBL4284771)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of human placental microsomal fraction 17beta-HSD2 using [3H]-E2 as substrate after 20 mins in presence of NAD+ by radio-flow detector bas...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 2(Homo sapiens (Human))
Pharmbiotec

Curated by ChEMBL
LigandPNGBDBM50466020(CHEMBL4293119)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of human placental microsomal fraction 17beta-HSD2 using [3H]-E2 as substrate after 20 mins in presence of NAD+ by radio-flow detector bas...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 2(Homo sapiens (Human))
Pharmbiotec

Curated by ChEMBL
LigandPNGBDBM50466012(CHEMBL4287575)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of human placental microsomal fraction 17beta-HSD2 using [3H]-E2 as substrate after 20 mins in presence of NAD+ by radio-flow detector bas...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 1(Homo sapiens (Human))
Pharmbiotec

Curated by ChEMBL
LigandPNGBDBM50466008(CHEMBL4290218)
Affinity DataIC50:  1.20nMAssay Description:Inhibition of human placental cytosolic 17beta-HSD1 using [3H]-E1 as substrate after 10 mins in presence of NADPH by radio-flow detector based analys...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 2(Homo sapiens (Human))
Pharmbiotec

Curated by ChEMBL
LigandPNGBDBM50466019(CHEMBL4286251)
Affinity DataIC50:  1.30nMAssay Description:Inhibition of human placental microsomal fraction 17beta-HSD2 using [3H]-E2 as substrate after 20 mins in presence of NAD+ by radio-flow detector bas...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 2(Homo sapiens (Human))
Pharmbiotec

Curated by ChEMBL
LigandPNGBDBM50466027(CHEMBL4292910)
Affinity DataIC50:  1.30nMAssay Description:Inhibition of human placental microsomal fraction 17beta-HSD2 using [3H]-E2 as substrate after 20 mins in presence of NAD+ by radio-flow detector bas...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 2(Homo sapiens (Human))
Pharmbiotec

Curated by ChEMBL
LigandPNGBDBM50232146(CHEMBL4092593)
Affinity DataIC50:  1.40nMAssay Description:Inhibition of human placental microsomal fraction 17beta-HSD2 using [3H]-E2 as substrate after 20 mins in presence of NAD+ by radio-flow detector bas...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 1(Homo sapiens (Human))
Pharmbiotec

Curated by ChEMBL
LigandPNGBDBM50466012(CHEMBL4287575)
Affinity DataIC50:  1.5nMAssay Description:Inhibition of human placental cytosolic 17beta-HSD1 using [3H]-E1 as substrate after 10 mins in presence of NADPH by radio-flow detector based analys...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 2(Homo sapiens (Human))
Pharmbiotec

Curated by ChEMBL
LigandPNGBDBM50466018(CHEMBL4283851)
Affinity DataIC50:  1.60nMAssay Description:Inhibition of human placental microsomal fraction 17beta-HSD2 using [3H]-E2 as substrate after 20 mins in presence of NAD+ by radio-flow detector bas...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 1(Homo sapiens (Human))
Pharmbiotec

Curated by ChEMBL
LigandPNGBDBM50466030(CHEMBL4291714)
Affinity DataIC50:  1.70nMAssay Description:Inhibition of human placental cytosolic 17beta-HSD1 using [3H]-E1 as substrate after 10 mins in presence of NADPH by radio-flow detector based analys...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
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