Compile Data Set for Download or QSAR
maximum 50k data
Found 88 with Last Name = 'baker' and Initial = 'b'
TargetMuscarinic acetylcholine receptor M5(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50403547(ATROPEN | ATROPINE)
Affinity DataKi:  0.400nMAssay Description:Displacement of [3H]QNB from muscarinic acetylcholine M5 receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50027065((5'alpha)-12'-hydroxy-2'-methyl-5'-(phenylmethyl)e...)
Affinity DataKi:  6nMAssay Description:Displacement of [3H]5-carboximidotryptamine from 5-HT1D receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

Target5-hydroxytryptamine receptor 5A(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50027065((5'alpha)-12'-hydroxy-2'-methyl-5'-(phenylmethyl)e...)
Affinity DataKi:  14nMAssay Description:Displacement of [3H]LSD from 5-HT5A receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent dopamine transporter(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM22165(1-{2-[bis(4-fluorophenyl)methoxy]ethyl}-4-(3-pheny...)
Affinity DataKi:  22nMAssay Description:Displacement of [3H]WIN35428 from DAT after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxy-tetrahydrodipicolinate reductase(Escherichia coli)
Triad Therapeutics

LigandPNGBDBM59098(Bi-ligand, 1)
Affinity DataKi:  26nMpH: 7.4Assay Description:All reactions were monitored spectrophotometrically at 340 nm by using initial rates from the first 5% of reaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 7(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50001888((chloropromazine) [3-(2-Chloro-phenothiazin-10-yl)...)
Affinity DataKi:  27nMAssay Description:Displacement of [3H]LSD from 5-HT7 receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

Target5-hydroxytryptamine receptor 2C(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50001888((chloropromazine) [3-(2-Chloro-phenothiazin-10-yl)...)
Affinity DataKi:  27nMAssay Description:Displacement of [3H]mesulergine from 5-HT2C receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetQuinone-dependent D-lactate dehydrogenase(Escherichia coli)
Triad Therapeutics

LigandPNGBDBM59099(Bi-ligand, 2)
Affinity DataKi:  42nMpH: 7.4Assay Description:All reactions were monitored spectrophotometrically at 340 nm by using initial rates from the first 5% of reaction.More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2B(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50353902(CHEMBL1829959)
Affinity DataKi:  88nMAssay Description:Displacement of [3H]LSD from 5-HT2B receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxy-tetrahydrodipicolinate reductase(Escherichia coli)
Triad Therapeutics

LigandPNGBDBM59101(Bi-ligand, 4)
Affinity DataKi:  100nMpH: 7.4Assay Description:All reactions were monitored spectrophotometrically at 340 nm by using initial rates from the first 5% of reaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(1B) dopamine receptor(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50004923((+/-)-SKF-38393 | 1-Phenyl-2,3,4,5-tetrahydro-1H-b...)
Affinity DataKi:  124nMAssay Description:Displacement of [3H]SCH233930 from dopamine D5 receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2B(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM10838(3-(2-aminopyrimidin-4-yl)-1H-indol-4-ol | Meridian...)
Affinity DataKi:  150nMAssay Description:Displacement of [3H]LSD from 5-HT2B receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target1-deoxy-D-xylulose 5-phosphate reductoisomerase(Escherichia coli)
Triad Therapeutics

LigandPNGBDBM59100(Bi-ligand, 3)
Affinity DataKi:  202nMpH: 7.4Assay Description:All reactions were monitored spectrophotometrically at 340 nm by using initial rates from the first 5% of reaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQuinone-dependent D-lactate dehydrogenase(Escherichia coli)
Triad Therapeutics

LigandPNGBDBM59101(Bi-ligand, 4)
Affinity DataKi:  620nMpH: 7.4Assay Description:All reactions were monitored spectrophotometrically at 340 nm by using initial rates from the first 5% of reaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM10838(3-(2-aminopyrimidin-4-yl)-1H-indol-4-ol | Meridian...)
Affinity DataKi:  684nMAssay Description:Displacement of [3H]8-OH-DPAT from 5-HT1A receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50353902(CHEMBL1829959)
Affinity DataKi:  1.35E+3nMAssay Description:Displacement of [3H]8-OH-DPAT from 5-HT1A receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 5A(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50353902(CHEMBL1829959)
Affinity DataKi:  1.53E+3nMAssay Description:Displacement of [3H]LSD from 5-HT5A receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 7(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50353902(CHEMBL1829959)
Affinity DataKi:  1.99E+3nMAssay Description:Displacement of [3H]LSD from 5-HT7 receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium-dependent dopamine transporter(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM10838(3-(2-aminopyrimidin-4-yl)-1H-indol-4-ol | Meridian...)
Affinity DataKi:  2.35E+3nMAssay Description:Displacement of [3H]WIN35428 from DAT after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMuscarinic acetylcholine receptor M5(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50353903(CHEMBL1829961)
Affinity DataKi:  7.04E+3nMAssay Description:Displacement of [3H]QNB from muscarinic acetylcholine M5 receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target1-deoxy-D-xylulose 5-phosphate reductoisomerase(Escherichia coli)
Triad Therapeutics

LigandPNGBDBM59101(Bi-ligand, 4)
Affinity DataKi:  7.90E+3nMpH: 7.4Assay Description:All reactions were monitored spectrophotometrically at 340 nm by using initial rates from the first 5% of reaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM10838(3-(2-aminopyrimidin-4-yl)-1H-indol-4-ol | Meridian...)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]5-carboximidotryptamine from 5-HT1D receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50353902(CHEMBL1829959)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]5-carboximidotryptamine from 5-HT1D receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target1-deoxy-D-xylulose 5-phosphate reductoisomerase(Escherichia coli)
Triad Therapeutics

LigandPNGBDBM59099(Bi-ligand, 2)
Affinity DataKi:  1.00E+4nMpH: 7.4Assay Description:All reactions were monitored spectrophotometrically at 340 nm by using initial rates from the first 5% of reaction.More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetD(1B) dopamine receptor(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50353903(CHEMBL1829961)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]SCH233930 from dopamine D5 receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2C(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50353902(CHEMBL1829959)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]mesulergine from 5-HT2C receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMuscarinic acetylcholine receptor M5(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM10838(3-(2-aminopyrimidin-4-yl)-1H-indol-4-ol | Meridian...)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]QNB from muscarinic acetylcholine M5 receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(1B) dopamine receptor(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50353901(CHEMBL1829958)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]SCH233930 from dopamine D5 receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(1B) dopamine receptor(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM10838(3-(2-aminopyrimidin-4-yl)-1H-indol-4-ol | Meridian...)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]SCH233930 from dopamine D5 receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(1B) dopamine receptor(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50353902(CHEMBL1829959)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]SCH233930 from dopamine D5 receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM50353901(CHEMBL1829958)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]5-carboximidotryptamine from 5-HT1D receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2C(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM10838(3-(2-aminopyrimidin-4-yl)-1H-indol-4-ol | Meridian...)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]mesulergine from 5-HT2C receptor after 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQuinone-dependent D-lactate dehydrogenase(Escherichia coli)
Triad Therapeutics

LigandPNGBDBM59100(Bi-ligand, 3)
Affinity DataKi:  1.20E+4nMpH: 7.4Assay Description:All reactions were monitored spectrophotometrically at 340 nm by using initial rates from the first 5% of reaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxy-tetrahydrodipicolinate reductase(Escherichia coli)
Triad Therapeutics

LigandPNGBDBM59100(Bi-ligand, 3)
Affinity DataKi: >2.50E+4nMpH: 7.4Assay Description:All reactions were monitored spectrophotometrically at 340 nm by using initial rates from the first 5% of reaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target1-deoxy-D-xylulose 5-phosphate reductoisomerase(Escherichia coli)
Triad Therapeutics

LigandPNGBDBM59098(Bi-ligand, 1)
Affinity DataKi: >5.00E+4nMpH: 7.4Assay Description:All reactions were monitored spectrophotometrically at 340 nm by using initial rates from the first 5% of reaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4-hydroxy-tetrahydrodipicolinate reductase(Escherichia coli)
Triad Therapeutics

LigandPNGBDBM59099(Bi-ligand, 2)
Affinity DataKi: >5.00E+4nMpH: 7.4Assay Description:All reactions were monitored spectrophotometrically at 340 nm by using initial rates from the first 5% of reaction.More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetQuinone-dependent D-lactate dehydrogenase(Escherichia coli)
Triad Therapeutics

LigandPNGBDBM59098(Bi-ligand, 1)
Affinity DataKi:  5.50E+4nMpH: 7.4Assay Description:All reactions were monitored spectrophotometrically at 340 nm by using initial rates from the first 5% of reaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Rattus norvegicus (rat))
Cv Technologies

Curated by ChEMBL
LigandPNGBDBM15579(CHEMBL972 | DEPRENYL | L-Deprenyl | N-methyl-N-[(2...)
Affinity DataIC50:  2.80nMAssay Description:In vitro ability of the compound to inhibit Monoamine oxidase B activity in rat whole brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Cv Technologies

Curated by ChEMBL
LigandPNGBDBM50105417(CHEMBL1089 | Nardil | PHENELZINE | Phenethyl-hydra...)
Affinity DataIC50:  30nMAssay Description:In vitro ability of the compound to inhibit Monoamine oxidase A activity in rat whole brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Rattus norvegicus (rat))
Cv Technologies

Curated by ChEMBL
LigandPNGBDBM50105417(CHEMBL1089 | Nardil | PHENELZINE | Phenethyl-hydra...)
Affinity DataIC50:  76nMAssay Description:In vitro ability of the compound to inhibit Monoamine oxidase B activity in rat whole brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Rattus norvegicus (rat))
Cv Technologies

Curated by ChEMBL
LigandPNGBDBM50105418(CHEMBL90144 | N-Phenethyl-N-prop-2-ynyl-hydrazine)
Affinity DataIC50:  77nMAssay Description:In vitro ability of the compound to inhibit Monoamine oxidase B activity in rat whole brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Rattus norvegicus (rat))
Cv Technologies

Curated by ChEMBL
LigandPNGBDBM50105423(CHEMBL90721 | N-Benzyl-N-prop-2-ynyl-hydrazine)
Affinity DataIC50:  121nMAssay Description:In vitro ability of the compound to inhibit Monoamine oxidase B activity in rat whole brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Cv Technologies

Curated by ChEMBL
LigandPNGBDBM50105421(CHEMBL89976 | N-Benzyl-N'-prop-2-ynyl-hydrazine)
Affinity DataIC50:  362nMAssay Description:In vitro ability of the compound to inhibit Monoamine oxidase A activity in rat whole brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Cv Technologies

Curated by ChEMBL
LigandPNGBDBM15579(CHEMBL972 | DEPRENYL | L-Deprenyl | N-methyl-N-[(2...)
Affinity DataIC50:  516nMAssay Description:In vitro ability of the compound to inhibit Monoamine oxidase A activity in rat whole brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Rattus norvegicus (rat))
Cv Technologies

Curated by ChEMBL
LigandPNGBDBM50105422(CHEMBL328446 | N-Phenyl-N-prop-2-ynyl-hydrazine)
Affinity DataIC50:  1.01E+3nMAssay Description:In vitro ability of the compound to inhibit Monoamine oxidase B activity in rat whole brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Cv Technologies

Curated by ChEMBL
LigandPNGBDBM50105416(CHEMBL328551 | N-((E)-3-Phenyl-allyl)-N-prop-2-yny...)
Affinity DataIC50:  1.17E+3nMAssay Description:In vitro ability of the compound to inhibit Monoamine oxidase A activity in rat whole brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
University Of South Florida

Curated by ChEMBL
LigandPNGBDBM10838(3-(2-aminopyrimidin-4-yl)-1H-indol-4-ol | Meridian...)
Affinity DataIC50:  1.30E+3nMAssay Description:Inhibition of GSK3-betaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Cv Technologies

Curated by ChEMBL
LigandPNGBDBM50105423(CHEMBL90721 | N-Benzyl-N-prop-2-ynyl-hydrazine)
Affinity DataIC50:  1.56E+3nMAssay Description:In vitro ability of the compound to inhibit Monoamine oxidase A activity in rat whole brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Cv Technologies

Curated by ChEMBL
LigandPNGBDBM50105420(CHEMBL90653 | N-Phenethyl-N'-prop-2-ynyl-hydrazine)
Affinity DataIC50:  1.85E+3nMAssay Description:In vitro ability of the compound to inhibit Monoamine oxidase A activity in rat whole brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Cv Technologies

Curated by ChEMBL
LigandPNGBDBM50105418(CHEMBL90144 | N-Phenethyl-N-prop-2-ynyl-hydrazine)
Affinity DataIC50:  2.04E+3nMAssay Description:In vitro ability of the compound to inhibit Monoamine oxidase A activity in rat whole brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Displayed 1 to 50 (of 88 total ) | Next | Last >>
Jump to: