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Found 1196 with Last Name = 'costi' and Initial = 'mp'
TargetDihydrofolate reductase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM66082((2S)-2-[[4-[(2,4-diaminopteridin-6-yl)methyl-methy...)
Affinity DataKi:  0.0100nMAssay Description:Inhibition of DHFR (unknown origin)More data for this Ligand-Target Pair
TargetThymidylate synthase(Lactobacillus casei)
Università

Curated by ChEMBL
LigandPNGBDBM50161776((S)-2-(5-Benzyloxycarbonylamino-naphthalene-1-sulf...)
Affinity DataKi:  0.100nMAssay Description:Inhibitory constant against thymidylate synthase from Lactobacillus caseiMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50161777((S)-3-[4-(5-Dimethylamino-naphthalene-1-sulfonylox...)
Affinity DataKi:  0.300nMAssay Description:Inhibitory constant against thymidylate synthase from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50161775((S)-2-(6-Amino-naphthalene-1-sulfonylamino)-3-[4-(...)
Affinity DataKi:  0.300nMAssay Description:Inhibitory constant against thymidylate synthase from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Lactobacillus casei)
Università

Curated by ChEMBL
LigandPNGBDBM50161777((S)-3-[4-(5-Dimethylamino-naphthalene-1-sulfonylox...)
Affinity DataKi:  0.300nMAssay Description:Inhibitory constant against thymidylate synthase from Lactobacillus caseiMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Lactobacillus casei)
Università

Curated by ChEMBL
LigandPNGBDBM50161775((S)-2-(6-Amino-naphthalene-1-sulfonylamino)-3-[4-(...)
Affinity DataKi:  0.5nMAssay Description:Inhibitory constant against thymidylate synthase from Lactobacillus caseiMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
Institute Of Theoretical Studies Ggmbh

Curated by ChEMBL
LigandPNGBDBM18796((2S)-2-{[4-(2-{2-amino-4-oxo-1H,4H,7H-pyrrolo[2,3-...)
Affinity DataKi:  1.30nMAssay Description:Inhibition of thymidin synthaseMore data for this Ligand-Target Pair
TargetThymidylate synthase(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50161780((S)-2-(4-Benzyloxycarbonylamino-naphthalene-1-sulf...)
Affinity DataKi:  1.5nMAssay Description:Inhibitory constant against thymidylate synthase from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
Institute Of Theoretical Studies Ggmbh

Curated by ChEMBL
LigandPNGBDBM50161778((S)-3-[4-(5-Dimethylamino-naphthalene-1-sulfonylox...)
Affinity DataKi:  1.5nMAssay Description:Inhibitory constant against human thymidylate synthaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Lactobacillus casei)
Università

Curated by ChEMBL
LigandPNGBDBM50161778((S)-3-[4-(5-Dimethylamino-naphthalene-1-sulfonylox...)
Affinity DataKi:  1.60nMAssay Description:Inhibitory constant against thymidylate synthase from Lactobacillus caseiMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Lactobacillus casei)
Università

Curated by ChEMBL
LigandPNGBDBM50161780((S)-2-(4-Benzyloxycarbonylamino-naphthalene-1-sulf...)
Affinity DataKi:  1.70nMAssay Description:Inhibitory constant against thymidylate synthase from Lactobacillus caseiMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
Institute Of Theoretical Studies Ggmbh

Curated by ChEMBL
LigandPNGBDBM50161777((S)-3-[4-(5-Dimethylamino-naphthalene-1-sulfonylox...)
Affinity DataKi:  4.10nMAssay Description:Inhibitory constant against human thymidylate synthaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM18796((2S)-2-{[4-(2-{2-amino-4-oxo-1H,4H,7H-pyrrolo[2,3-...)
Affinity DataKi:  7.20nMAssay Description:Inhibition of DHFRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
Institute Of Theoretical Studies Ggmbh

Curated by ChEMBL
LigandPNGBDBM50161775((S)-2-(6-Amino-naphthalene-1-sulfonylamino)-3-[4-(...)
Affinity DataKi:  8.5nMAssay Description:Inhibitory constant against human thymidylate synthaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50161776((S)-2-(5-Benzyloxycarbonylamino-naphthalene-1-sulf...)
Affinity DataKi:  9.40nMAssay Description:Inhibitory constant against thymidylate synthase from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50225373(CHEMBL396872 | pinacol 5-[(3,4-dichlorophenylamino...)
Affinity DataKi:  10nMAssay Description:Inhibition of Escherichia coli beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50433811(CHEMBL2382332)
Affinity DataKi:  11nMAssay Description:Inhibition of human DHFR using dihydrofolate as substrate after 180 secs by spectrophotometric analysisMore data for this Ligand-Target Pair
TargetThymidylate synthase(Homo sapiens (Human))
Institute Of Theoretical Studies Ggmbh

Curated by ChEMBL
LigandPNGBDBM50161780((S)-2-(4-Benzyloxycarbonylamino-naphthalene-1-sulf...)
Affinity DataKi:  11nMAssay Description:Inhibitory constant against human thymidylate synthaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
Institute Of Theoretical Studies Ggmbh

Curated by ChEMBL
LigandPNGBDBM50161776((S)-2-(5-Benzyloxycarbonylamino-naphthalene-1-sulf...)
Affinity DataKi:  13nMAssay Description:Inhibitory constant against human thymidylate synthaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
Institute Of Theoretical Studies Ggmbh

Curated by ChEMBL
LigandPNGBDBM50022238((R)-5-Fluoro-1-((4S,5R)-4-hydroxy-5-methylphosphat...)
Affinity DataKi:  14nMAssay Description:Inhibition of human thymidylate synthase expressed in Escherichia coli incubated for 1 hr by spectrophotometryMore data for this Ligand-Target Pair
TargetThymidylate synthase(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50161778((S)-3-[4-(5-Dimethylamino-naphthalene-1-sulfonylox...)
Affinity DataKi:  15nMAssay Description:Inhibitory constant against thymidylate synthase from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM26139(1-benzothiophen-2-ylboranediol | 1-benzothiophen-2...)
Affinity DataKi:  27nMAssay Description:Inhibition of Escherichia coli beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50225393(CHEMBL235526 | pinacol 5-[(carboxymethylamino)meth...)
Affinity DataKi:  28nMAssay Description:Inhibition of Escherichia coli beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50225381(CHEMBL235293 | pinacol5-{[4-(1-hydroxy-2,2,2-trifl...)
Affinity DataKi:  28nMAssay Description:Inhibition of Escherichia coli beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase, mitochondrial(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50123588(CHEMBL297258)
Affinity DataKi:  29nMAssay Description:Competitive inhibition of human FolD dehydrogenase activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50225376(CHEMBL397522 | pinacol 5-bromomethylbenzo[b]thioph...)
Affinity DataKi:  30nMAssay Description:Inhibition of Escherichia coli beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
Institute Of Theoretical Studies Ggmbh

Curated by ChEMBL
LigandPNGBDBM18771((2S)-2-[(4-{[(2-amino-4-oxo-1,4-dihydroquinazolin-...)
Affinity DataKi:  30nMAssay Description:TS was assayed spectrophotometrically in the reaction buffer solution containing (6R, 6S)-5, 10-CH2H4folate. The reaction was initiated by the additi...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50225371(5-methyl-benzo[b]thiophen-2-ylboronic acid | CHEMB...)
Affinity DataKi:  30nMAssay Description:Inhibition of Escherichia coli beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50225379(CHEMBL235292 | pinacol 5-[(3-nitrophenylamino)meth...)
Affinity DataKi:  37nMAssay Description:Inhibition of Escherichia coli beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50225378(CHEMBL235073 | pinacol 5-diformylaminomethylbenzo[...)
Affinity DataKi:  37nMAssay Description:Inhibition of Escherichia coli beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50225392(5-hydroxymethylbenzo[b]thiophen-2-ylboronic acid |...)
Affinity DataKi:  43nMAssay Description:Inhibition of Escherichia coli beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50225380(CHEMBL235308 | pinacol 5-[(phenylamino3-boronicaci...)
Affinity DataKi:  45nMAssay Description:Inhibition of Escherichia coli beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Escherichia coli)
Unimore

LigandPNGBDBM18771((2S)-2-[(4-{[(2-amino-4-oxo-1,4-dihydroquinazolin-...)
Affinity DataKi:  60nMAssay Description:TS was assayed spectrophotometrically in the reaction buffer solution containing (6R, 6S)-5, 10-CH2H4folate. The reaction was initiated by the additi...More data for this Ligand-Target Pair
TargetThymidylate synthase(Lactobacillus casei)
Università

Curated by ChEMBL
LigandPNGBDBM18771((2S)-2-[(4-{[(2-amino-4-oxo-1,4-dihydroquinazolin-...)
Affinity DataKi:  60nM ΔG°:  -40.5kJ/molepH: 7.4 T: 2°CAssay Description:TS was assayed spectrophotometrically in the reaction buffer solution containing (6R, 6S)-5, 10-CH2H4folate. The reaction was initiated by the additi...More data for this Ligand-Target Pair
TargetBeta-lactamase(Escherichia coli)
Northwestern University

LigandPNGBDBM39849(Amide and sulfonamide derivatives, 33)
Affinity DataKi:  60nMpH: 7.0Assay Description:Inhibition assay against beta lactamase enzymes.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50405066(CHEMBL268088)
Affinity DataKi:  70nMAssay Description:Inhibition of human DHFR using dihydrofolate as substrate after 180 secs by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Escherichia coli)
Northwestern University

LigandPNGBDBM50115616(3-(4-BENZENESULFONYL-THIOPHENE-2-SULFONYLAMINO)-PH...)
Affinity DataKi:  80nMpH: 7.0Assay Description:Inhibition assay against beta lactamase enzymes.More data for this Ligand-Target Pair
TargetBeta-lactamase(Escherichia coli)
Northwestern University

LigandPNGBDBM39856(Amide and sulfonamide derivatives, 41)
Affinity DataKi:  80nMpH: 7.0Assay Description:Inhibition assay against beta lactamase enzymes.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50225383(CHEMBL236203 | pinacol 5-phenylsulphanylmethylbenz...)
Affinity DataKi:  80nMAssay Description:Inhibition of Escherichia coli beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Escherichia coli)
Northwestern University

LigandPNGBDBM50115616(3-(4-BENZENESULFONYL-THIOPHENE-2-SULFONYLAMINO)-PH...)
Affinity DataKi:  80nMAssay Description:Apparent inhibition constant against Escherichia coli AmpC beta-lactamaseMore data for this Ligand-Target Pair
TargetBeta-lactamase TEM(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50225389(5-imidazol-1-yl-methylbenzo[b]thiophen-2-ylboronic...)
Affinity DataKi:  82nMAssay Description:Inhibition of Escherichia coli beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50225377(CHEMBL237390 | pinacol 5-(3,4-dichlorophenoxymethy...)
Affinity DataKi:  83nMAssay Description:Inhibition of Escherichia coli beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50251158(2-[(3,4,5-Trimethoxy-phenyl)amino]-3-phenyl-5,7-di...)
Affinity DataKi:  100nMAssay Description:Inhibition of human dihydrofolate reductaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Escherichia coli)
Northwestern University

LigandPNGBDBM39819(Amide and sulfonamide derivatives, 3)
Affinity DataKi:  100nMpH: 7.0Assay Description:Inhibition assay against beta lactamase enzymes.More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50090054(1-(3-Chloro-phenyl)-6,6-dimethyl-1,6-dihydro-[1,3,...)
Affinity DataKi:  100nMAssay Description:Inhibition of human DHFR using dihydrofolate as substrate after 180 secs by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50090069(1-(3,4-Dichloro-phenyl)-6,6-dimethyl-1,6-dihydro-[...)
Affinity DataKi:  110nMAssay Description:Inhibition of human DHFR using dihydrofolate as substrate after 180 secs by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Escherichia coli)
Northwestern University

LigandPNGBDBM39820(Amide and sulfonamide derivatives, 4)
Affinity DataKi:  120nMpH: 7.0Assay Description:Inhibition assay against beta lactamase enzymes.More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDihydrofolate reductase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50291793(6,6-Dimethyl-1-(3-trifluoromethyl-phenyl)-1,6-dihy...)
Affinity DataKi:  130nMAssay Description:Inhibition of human DHFR using dihydrofolate as substrate after 180 secs by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Northwestern University

LigandPNGBDBM39856(Amide and sulfonamide derivatives, 41)
Affinity DataKi:  170nMpH: 7.0Assay Description:Inhibition assay against beta lactamase enzymes.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Università

Curated by ChEMBL
LigandPNGBDBM50225374(5 [(1,2,4-triazol-1-ylmethyl]benzo[b]thiophen-2-yl...)
Affinity DataKi:  170nMAssay Description:Inhibition of Escherichia coli beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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