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Found 267 with Last Name = 'sergheraert' and Initial = 'c'
TargetcAMP-dependent protein kinase catalytic subunit gamma(Homo sapiens (Human))
Ura Cnrs 1309

Curated by ChEMBL
LigandPNGBDBM50228843(CHEMBL436718)
Affinity DataKi:  4nMAssay Description:Displacement of ATP from protein kinase A (PKA)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-dependent protein kinase catalytic subunit gamma(Homo sapiens (Human))
Ura Cnrs 1309

Curated by ChEMBL
LigandPNGBDBM50228839(CHEMBL415414)
Affinity DataKi:  170nMAssay Description:Displacement of ATP from protein kinase A (PKA)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-dependent protein kinase catalytic subunit gamma(Homo sapiens (Human))
Ura Cnrs 1309

Curated by ChEMBL
LigandPNGBDBM50216682(1-(5-Isoquinolinesulfonyl)-2-methylpiperazine | 1-...)
Affinity DataKi:  3.00E+3nMAssay Description:Displacement of ATP from protein kinase A (PKA)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50216682(1-(5-Isoquinolinesulfonyl)-2-methylpiperazine | 1-...)
Affinity DataKi:  6.00E+3nMAssay Description:Displacement of ATP from protein kinase C (PKC)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrypanothione reductase(Trypanosoma cruzi)
TBA

Curated by ChEMBL
LigandPNGBDBM50280883((2-(2-Benzyloxycarbonylamino-2-{[(3-dimethylamino-...)
Affinity DataKi:  3.10E+4nMAssay Description:Compound was tested for inhibitory activity against recombinant Trypanothione reductase from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTrypanothione reductase(Trypanosoma cruzi)
TBA

Curated by ChEMBL
LigandPNGBDBM50280882((3-(2-Benzyloxycarbonylamino-2-{[(3-dimethylamino-...)
Affinity DataKi:  4.30E+4nMAssay Description:Compound was tested for inhibitory activity against recombinant Trypanothione reductase from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTrypanothione reductase(Trypanosoma cruzi)
TBA

Curated by ChEMBL
LigandPNGBDBM50280881((2-(2-Benzyloxycarbonylamino-2-{[(3-dimethylamino-...)
Affinity DataKi:  9.20E+4nMAssay Description:Compound was tested for inhibitory activity against recombinant Trypanothione reductase from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails Article
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172914((S)-2-(2-Piperidin-1-yl-ethyl)-3-thioxo-2,3,10,10a...)
Affinity DataIC50:  0.900nMAssay Description:Inhibitory concentration against opioid receptor sigma 1 of guinea pig cerebral cortex using [3H]-(+)-pentazocine upon incubation for 150 minutes at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM21398(4-[4-(4-Chloro-phenyl)-4-hydroxy-piperidin-1-yl]-1...)
Affinity DataIC50:  2.10nMAssay Description:Inhibitory concentration against opioid receptor sigma 1 of guinea pig cerebral cortex using [3H]-(+)-pentazocine upon incubation for 150 minutes at ...More data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172886((S)-2-[3-(Methyl-phenethyl-amino)-propyl]-10,10a-d...)
Affinity DataIC50:  2.10nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM21398(4-[4-(4-Chloro-phenyl)-4-hydroxy-piperidin-1-yl]-1...)
Affinity DataIC50:  2.10nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172884((S)-2-(1-Benzyl-piperidin-4-yl)-10,10a-dihydro-5H-...)
Affinity DataIC50:  2.40nMpH: 7.5 T: 2°CAssay Description:Inhibitory activity against Opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172874((S)-2-{2-[Methyl-(5-phenyl-pentyl)-amino]-ethyl}-1...)
Affinity DataIC50:  2.90nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-dependent protein kinase catalytic subunit gamma(Homo sapiens (Human))
Ura Cnrs 1309

Curated by ChEMBL
LigandPNGBDBM50228843(CHEMBL436718)
Affinity DataIC50:  3nMAssay Description:Inhibition of cAMP-dependent protein kinase (PKA).More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172869((S)-2-{2-[Methyl-(4-phenyl-butyl)-amino]-ethyl}-10...)
Affinity DataIC50:  3.20nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVasopressin V2 receptor(Sus scrofa)
TBA

Curated by ChEMBL
LigandPNGBDBM35667(AVP | CHEMBL373742 | US10131692, 44 (AVP) | [3H]Ar...)
Affinity DataIC50:  3.30nMAssay Description:Tested for the inhibition to V2 subtype receptor using [3H]- (VS2) as radioligand at 3 nM and arginine-vasopressin at 2 microM in LLCPKI cellsMore data for this Ligand-Target Pair
In DepthDetails Article
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172868((S)-2-(3-(benzyl(methyl)amino)propyl)-10,10a-dihyd...)
Affinity DataIC50:  3.90nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172875((S)-2-[4-(Benzyl-methyl-amino)-butyl]-10,10a-dihyd...)
Affinity DataIC50:  4.20nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172881((S)-2-[2-(Benzyl-methyl-amino)-ethyl]-10,10a-dihyd...)
Affinity DataIC50:  4.5nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172880((S)-2-[5-(Benzyl-methyl-amino)-pentyl]-10,10a-dihy...)
Affinity DataIC50:  5nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172877((S)-2-(2-Piperidin-1-yl-ethyl)-10,10a-dihydro-5H-i...)
Affinity DataIC50:  6.60nMAssay Description:Inhibitory concentration against opioid receptor sigma 1 of guinea pig cerebral cortex using [3H]-(+)-pentazocine upon incubation for 150 minutes at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistidine-rich protein PFHRP-II(Plasmodium falciparum)
Universit£

Curated by ChEMBL
LigandPNGBDBM50123594((7-Chloro-quinolin-4-yl)-{3-[4-(3-dibutylamino-pro...)
Affinity DataIC50:  6.70nMAssay Description:In vitro inhibition of beta-hematin formationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProlyl endopeptidase(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50075135((S)-4-phenyl-1-(3-(pyrrolidine-1-carbonyl)-3,4-dih...)
Affinity DataIC50:  7nMAssay Description:Inhibition of Prolyl endopeptidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProlyl endopeptidase(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50075132(2-(4-Methyl-cyclohexyl)-1-[(S)-3-(pyrrolidine-1-ca...)
Affinity DataIC50:  9nMAssay Description:Inhibition of Prolyl endopeptidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172887((S)-2-[6-(Benzyl-methyl-amino)-hexyl]-10,10a-dihyd...)
Affinity DataIC50:  9.40nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVasopressin V2 receptor(Sus scrofa)
TBA

Curated by ChEMBL
LigandPNGBDBM50291329(8-arginine vasopressin trisulphide | CHEMBL267405)
Affinity DataIC50:  9.5nMAssay Description:Tested for the inhibition to V2 subtype receptor using [3H]- (VS2) as radioligand at 3 nM and arginine-vasopressin at 2 microM in LLCPKI cellsMore data for this Ligand-Target Pair
In DepthDetails Article
TargetVasopressin V1a/V1b receptor(RAT)
TBA

Curated by ChEMBL
LigandPNGBDBM50291329(8-arginine vasopressin trisulphide | CHEMBL267405)
Affinity DataIC50:  9.5nMAssay Description:Tested for the TYR(Me)2 arginine-vasopressin as radioligand at 0.3 nM in A7r5 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172871((S)-2-(3-Benzylamino-propyl)-10,10a-dihydro-5H-imi...)
Affinity DataIC50:  9.60nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172876((S)-2-[4-(Methyl-phenethyl-amino)-butyl]-10,10a-di...)
Affinity DataIC50:  9.90nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVasopressin V1a/V1b receptor(RAT)
TBA

Curated by ChEMBL
LigandPNGBDBM35667(AVP | CHEMBL373742 | US10131692, 44 (AVP) | [3H]Ar...)
Affinity DataIC50:  10nMAssay Description:Tested for the TYR(Me)2 arginine-vasopressin as radioligand at 0.3 nM in A7r5 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172873((S)-2-[3-(4-Phenyl-butylamino)-propyl]-10,10a-dihy...)
Affinity DataIC50:  10.5nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172893((S)-2-[5-(Methyl-phenethyl-amino)-pentyl]-10,10a-d...)
Affinity DataIC50:  11.7nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172867((S)-2-[2-(Methyl-phenethyl-amino)-ethyl]-10,10a-di...)
Affinity DataIC50:  12.6nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172888((S)-2-{2-[Methyl-(3-phenyl-propyl)-amino]-ethyl}-1...)
Affinity DataIC50:  13.6nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProlyl endopeptidase(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50075126(5-Phenyl-1-[(S)-3-(pyrrolidine-1-carbonyl)-3,4-dih...)
Affinity DataIC50:  14nMAssay Description:Inhibition of Prolyl endopeptidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistidine-rich protein PFHRP-II(Plasmodium falciparum)
Universit£

Curated by ChEMBL
LigandPNGBDBM50123579(CHEMBL345958 | [3-(4-{3-[Bis-(4-nitro-benzyl)-amin...)
Affinity DataIC50:  15nMAssay Description:In vitro inhibition of beta-hematin formationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProlyl endopeptidase(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50051539((S)-4-phenyl-1-(2-(pyrrolidine-1-carbonyl)pyrrolid...)
Affinity DataIC50:  15nMAssay Description:Inhibition of Prolyl endopeptidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172877((S)-2-(2-Piperidin-1-yl-ethyl)-10,10a-dihydro-5H-i...)
Affinity DataIC50:  16nMAssay Description:Inhibitory concentration against opioid receptor sigma 1 of guinea pig cerebral cortex using [3H]-(+)-pentazocine upon incubation for 150 minutes at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172877((S)-2-(2-Piperidin-1-yl-ethyl)-10,10a-dihydro-5H-i...)
Affinity DataIC50:  16nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProlyl endopeptidase(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50075134(4-(4-Chloro-2-methyl-phenoxy)-1-[(S)-3-(pyrrolidin...)
Affinity DataIC50:  17nMAssay Description:Inhibition of Prolyl endopeptidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProlyl endopeptidase(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50075129(1-[(S)-3-(Pyrrolidine-1-carbonyl)-3,4-dihydro-1H-i...)
Affinity DataIC50:  21nMAssay Description:Inhibition of Prolyl endopeptidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProlyl endopeptidase(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50075128(CHEMBL138674 | {6-Oxo-6-[(S)-3-(pyrrolidine-1-carb...)
Affinity DataIC50:  21nMAssay Description:Inhibition of Prolyl endopeptidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172879((S)-2-(3-Piperidin-1-yl-propyl)-10,10a-dihydro-5H-...)
Affinity DataIC50:  21.5nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172879((S)-2-(3-Piperidin-1-yl-propyl)-10,10a-dihydro-5H-...)
Affinity DataIC50:  21.5nMAssay Description:Inhibitory concentration against opioid receptor sigma 1 of guinea pig cerebral cortex using [3H]-(+)-pentazocine upon incubation for 150 minutes at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProlyl endopeptidase(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50075125(((1S,2S)-2-Phenyl-cyclopropyl)-[(S)-3-(pyrrolidine...)
Affinity DataIC50:  23nMAssay Description:Inhibition of Prolyl endopeptidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistidine-rich protein PFHRP-II(Plasmodium falciparum)
Universit£

Curated by ChEMBL
LigandPNGBDBM50123587((7-Chloro-quinolin-4-yl)-(3-{4-[3-(cyclopropylmeth...)
Affinity DataIC50:  23.3nMAssay Description:In vitro inhibition of beta-hematin formationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistidine-rich protein PFHRP-II(Plasmodium falciparum)
Universit£

Curated by ChEMBL
LigandPNGBDBM50409777(CHEMBL2111198)
Affinity DataIC50:  23.5nMAssay Description:In vitro inhibition of beta-hematin formationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50172889((S)-2-[3-(4-Benzo[1,3]dioxol-5-ylmethyl-piperazin-...)
Affinity DataIC50:  23.8nMpH: 7.5Assay Description:Inhibitory activity against opioid receptor sigma 1 in guinea pig cerebral cortex using [3H]-(+)-pentazocine as radio ligand at pH 7.5 for 150 min at...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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