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Found 168 with Last Name = 'debreu' and Initial = 'ma'
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
TargetHistidine-rich protein PFHRP-II(Plasmodium falciparum)
Universit£

Curated by ChEMBL
LigandPNGBDBM50123575((3-{4-[3-(Bis-cyclopropylmethyl-amino)-propyl]-pip...)
Affinity DataIC50:  27.1nMAssay 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
LigandPNGBDBM50172885((S)-2-[6-(Methyl-phenethyl-amino)-hexyl]-10,10a-di...)
Affinity DataIC50:  29.5nMpH: 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
LigandPNGBDBM50172872((S)-2-[3-(4-Benzyl-piperazin-1-yl)-propyl]-10,10a-...)
Affinity DataIC50:  32nMpH: 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
TargetHistidine-rich protein PFHRP-II(Plasmodium falciparum)
Universit£

Curated by ChEMBL
LigandPNGBDBM50123577(CHEMBL152862 | Cyclopropanecarboxylic acid (3-{4-[...)
Affinity DataIC50:  34nMAssay 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
LigandPNGBDBM50123561(CHEMBL149751 | N-(3-(4-(3-(7-chloroquinolin-4-ylam...)
Affinity DataIC50:  34.2nMAssay 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
LigandPNGBDBM50123569(CHEMBL357111 | N-(3-{4-[3-(7-Chloro-quinolin-4-yla...)
Affinity DataIC50:  35.6nMAssay 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
LigandPNGBDBM50123558((7-Chloro-quinolin-4-yl)-(3-{4-[3-(3-phenoxy-benzy...)
Affinity DataIC50:  37.5nMAssay 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
LigandPNGBDBM50123571((7-Chloro-quinolin-4-yl)-(3-{4-[3-(4-nitro-benzyla...)
Affinity DataIC50:  40nMAssay 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
LigandPNGBDBM50123562(CHEMBL152635 | N-(3-(4-(3-(7-chloroquinolin-4-ylam...)
Affinity DataIC50:  40.2nMAssay 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
LigandPNGBDBM50123565((7-Chloro-quinolin-4-yl)-[3-(4-{3-[(quinolin-4-ylm...)
Affinity DataIC50:  42.5nMAssay 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
LigandPNGBDBM50123572((3-{4-[3-(Bis-quinolin-4-ylmethyl-amino)-propyl]-p...)
Affinity DataIC50:  43.4nMAssay 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
LigandPNGBDBM50123613(CHEMBL152886 | [3-(4-{3-[Bis-(4-methoxy-benzyl)-am...)
Affinity DataIC50:  47.8nMAssay 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
LigandPNGBDBM50123582(CHEMBL422682 | N-(3-(4-(3-(7-chloroquinolin-4-ylam...)
Affinity DataIC50:  50.6nMAssay 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
LigandPNGBDBM50123566(CHEMBL356249 | N-(3-(4-(3-(butylamino)propyl)piper...)
Affinity DataIC50:  50.9nMAssay 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
LigandPNGBDBM50172912((S)-2-(2-Piperidin-1-yl-ethyl)-1,5,10,10a-tetrahyd...)
Affinity DataIC50:  54nMAssay 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
LigandPNGBDBM50123585((7-Chloro-quinolin-4-yl)-(3-{4-[3-(4-methoxy-benzy...)
Affinity DataIC50:  61.4nMAssay 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
LigandPNGBDBM50172911((S)-2-(3-Piperidin-1-yl-propyl)-9,9a-dihydro-imida...)
Affinity DataIC50:  66nMAssay 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
LigandPNGBDBM50123574(CHEMBL346177 | [3-(4-{3-[Bis-(4-phenoxy-benzyl)-am...)
Affinity DataIC50:  74.9nMAssay 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
LigandPNGBDBM22985(Aralen | CHEMBL76 | CHLOROQUINE PHOSPHATE | Chloro...)
Affinity DataIC50:  76.5nMAssay Description:Inhibitory activity against 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
LigandPNGBDBM50172915((S)-2-(2-Piperidin-1-yl-ethyl)-1,2,3,5,10,10a-hexa...)
Affinity DataIC50:  77nMAssay 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
LigandPNGBDBM50123604(CHEMBL152266 | N-(3-(4-(3-(7-chloroquinolin-4-ylam...)
Affinity DataIC50:  79nMAssay 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
LigandPNGBDBM50172891((S)-2-[3-(1-Benzyl-piperidin-4-ylamino)-propyl]-10...)
Affinity DataIC50:  82.3nMpH: 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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