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Found 140 with Last Name = 'schwartz' and Initial = 'ce'
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50142873(CHEMBL53070 | {(4bS,8aR)-4b-[2-(tert-Butoxycarbony...)
Affinity DataKi:  14nMAssay Description:Inhibition of [3H](+)-pentazocine binding to Sigma receptor type 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50142868(CHEMBL51146 | CHEMBL540283 | {[2-((4aS,10aR)-6-Met...)
Affinity DataKi:  37nMAssay Description:Inhibition of [3H](+)-pentazocine binding to Sigma receptor type 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50142871(Allyl-[2-((4aS,10aR)-6-methoxy-1,3,4,10a-tetrahydr...)
Affinity DataKi:  49nMAssay Description:Inhibition of [3H](+)-pentazocine binding to Sigma receptor type 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50142866((2-Methoxy-ethyl)-[2-((4aS,10aR)-6-methoxy-1,3,4,1...)
Affinity DataKi:  49nMAssay Description:Inhibition of [3H](+)-pentazocine binding to Sigma receptor type 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50142869(CHEMBL301772 | {(4bR,8aS)-4b-[2-(tert-Butoxycarbon...)
Affinity DataKi:  115nMAssay Description:Inhibition of [3H](+)-pentazocine binding to Sigma receptor type 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50142867(2-{[2-((4aS,10aR)-6-Methoxy-1,3,4,10a-tetrahydro-2...)
Affinity DataKi:  161nMAssay Description:Inhibition of [3H](+)-pentazocine binding to Sigma receptor type 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50142864((2-Benzyloxy-ethyl)-[2-((4aS,10aR)-6-methoxy-1,3,4...)
Affinity DataKi:  241nMAssay Description:Inhibition of [3H](+)-pentazocine binding to Sigma receptor type 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50142870(CHEMBL545668 | [2-((4aS,10aR)-6-Methoxy-1,3,4,10a-...)
Affinity DataKi:  245nMAssay Description:Inhibition of [3H](+)-pentazocine binding to Sigma receptor type 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50366613(DEXTROMETHORPHAN)
Affinity DataKi:  348nMAssay Description:Inhibition of [3H](+)-pentazocine binding to Sigma receptor type 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50142868(CHEMBL51146 | CHEMBL540283 | {[2-((4aS,10aR)-6-Met...)
Affinity DataKi:  373nMAssay Description:Inhibition of [3H](+)-pentazocine binding to Sigma receptor type 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50142863(CHEMBL298778 | [2-((4aS,10aR)-6-Methoxy-1,3,4,10a-...)
Affinity DataKi:  456nMAssay Description:Inhibition of [3H](+)-pentazocine binding to Sigma receptor type 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50142874(CHEMBL299327 | N-{2-[(4aS,10aR)-6-methoxy-1,2,3,4,...)
Affinity DataKi: >3.30E+3nMAssay Description:Inhibition of [3H](+)-pentazocine binding to Sigma receptor type 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50142875(CHEMBL301487 | [2-((4aS,10aR)-6-Methoxy-1,3,4,10a-...)
Affinity DataKi: >3.30E+3nMAssay Description:Inhibition of [3H](+)-pentazocine binding to Sigma receptor type 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50059858((S)-2-((3Z,6E)-(2S,5S,8R)-8-Amino-2-benzyl-5-isopr...)
Affinity DataIC50:  1nMAssay Description:In vitro inhibitory activity against Geranylgeranyl transferase in the geranylgeranylation of H-ras-CAIL proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha(Bos taurus (bovine))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM50079813(2-[1-[5-amino-6-sulfanyl-(5R)-hexanoyl]-4-phenoxy-...)
Affinity DataIC50:  2nMAssay Description:Inhibitory concentration was evaluated against Farnesyltransferase in the farnesylation of H-ras proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50079803((S)-2-{[(2S,4S)-1-((E)-(2S,5R)-5-Amino-2-isopropyl...)
Affinity DataIC50:  11nMAssay Description:In vitro inhibitory activity against Geranylgeranyl transferase in the geranylgeranylation of H-ras-CAIL proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha(Bos taurus (bovine))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM50079810(2-[1-[5-amino-2-isopropyl-6-sulfanyl-(2S,3E,5R)-3-...)
Affinity DataIC50:  17nMAssay Description:Inhibitory concentration was evaluated against Farnesyltransferase in the farnesylation of H-ras proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha(Bos taurus (bovine))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM50079803((S)-2-{[(2S,4S)-1-((E)-(2S,5R)-5-Amino-2-isopropyl...)
Affinity DataIC50:  18nMAssay Description:Inhibitory concentration was evaluated against Farnesyltransferase in the farnesylation of H-ras proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha(Bos taurus (bovine))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM50079786(2-[1-[5-amino-6-sulfanyl-(5R)-hexyl]-4-phenoxy-(2S...)
Affinity DataIC50:  20nMAssay Description:Inhibitory concentration was evaluated against Farnesyltransferase in the farnesylation of H-ras proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha(Bos taurus (bovine))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM50079793(2-[1-[5-amino-6-sulfanyl-(E,5R)-3-hexenyl]-4-pheno...)
Affinity DataIC50:  20nMAssay Description:Inhibitory concentration was evaluated against Farnesyltransferase in the farnesylation of H-ras proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha(Bos taurus (bovine))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM50059858((S)-2-((3Z,6E)-(2S,5S,8R)-8-Amino-2-benzyl-5-isopr...)
Affinity DataIC50:  26nMAssay Description:Inhibitory concentration was evaluated against Farnesyltransferase in the farnesylation of H-ras proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha(Bos taurus (bovine))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM50079804(2-[1-[4-amino-5-sulfanyl-(E,4R)-2-pentenyl]-4-(4-p...)
Affinity DataIC50:  35nMAssay Description:Inhibitory concentration was evaluated against Farnesyltransferase in the farnesylation of H-ras proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50079787(CHEMBL303859 | methyl 2-[1-[5-amino-2-isopropyl-6-...)
Affinity DataIC50:  40nMAssay Description:Inhibitory concentration against Farnesyltransferase for Farnesylation of H-ras protein InNIH 3T3 cells transformed with activated H-rasMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha(Bos taurus (bovine))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM50079809((S)-2-{[(2S,4S)-1-((E)-(R)-4-Amino-5-mercapto-pent...)
Affinity DataIC50:  47nMAssay Description:Inhibitory concentration was evaluated against Farnesyltransferase in the farnesylation of H-ras proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50403711(CHEMBL2092855)
Affinity DataIC50:  53nMAssay Description:In vitro inhibitory activity against Geranylgeranyl transferase in the geranylgeranylation of H-ras-CAIL proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha(Bos taurus (bovine))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM50403711(CHEMBL2092855)
Affinity DataIC50:  57nMAssay Description:In vitro inhibitory activity against Geranylgeranyl transferase in the geranylgeranylation of H-ras-CAIL proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha(Bos taurus (bovine))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM50079811(2-[1-[4-amino-5-sulfanyl-(E,4R)-2-pentenyl]-4-(4-i...)
Affinity DataIC50:  82nMAssay Description:Inhibitory concentration was evaluated against Farnesyltransferase in the farnesylation of H-ras proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha(Bos taurus (bovine))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM50079792(2-[1-[4-amino-5-sulfanyl-(E,4R)-2-pentenyl]-4-(4-b...)
Affinity DataIC50:  87nMAssay Description:Inhibitory concentration was evaluated against Farnesyltransferase in the farnesylation of H-ras proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50079809((S)-2-{[(2S,4S)-1-((E)-(R)-4-Amino-5-mercapto-pent...)
Affinity DataIC50:  89nMAssay Description:In vitro inhibitory activity against Geranylgeranyl transferase in the geranylgeranylation of H-ras-CAIL proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50079813(2-[1-[5-amino-6-sulfanyl-(5R)-hexanoyl]-4-phenoxy-...)
Affinity DataIC50:  100nMAssay Description:In vitro inhibitory activity against Geranylgeranyl transferase in the geranylgeranylation of H-ras-CAIL proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha(Bos taurus (bovine))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM50216999(CHEMBL3349357)
Affinity DataIC50:  100nMAssay Description:Inhibitory concentration was evaluated against Farnesyltransferase in the farnesylation of H-ras proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha(Bos taurus (bovine))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM50079794(2-[1-[4-amino-5-sulfanyl-(E,4R)-2-pentenyl]-4-(4-t...)
Affinity DataIC50:  110nMAssay Description:Inhibitory concentration was evaluated against Farnesyltransferase in the farnesylation of H-ras proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50079794(2-[1-[4-amino-5-sulfanyl-(E,4R)-2-pentenyl]-4-(4-t...)
Affinity DataIC50:  110nMAssay Description:In vitro inhibitory activity against Geranylgeranyl transferase in the geranylgeranylation of H-ras-CAIL proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50079810(2-[1-[5-amino-2-isopropyl-6-sulfanyl-(2S,3E,5R)-3-...)
Affinity DataIC50:  150nMAssay Description:In vitro inhibitory activity against Geranylgeranyl transferase in the geranylgeranylation of H-ras-CAIL proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50079806(2-[1-[4-amino-5-sulfanyl-(E,4R)-2-pentenyl]-4-(2-p...)
Affinity DataIC50:  170nMAssay Description:Inhibitory concentration against Farnesyltransferase for Farnesylation of H-ras protein InNIH 3T3 cells transformed with activated H-rasMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50079792(2-[1-[4-amino-5-sulfanyl-(E,4R)-2-pentenyl]-4-(4-b...)
Affinity DataIC50:  180nMAssay Description:In vitro inhibitory activity against Geranylgeranyl transferase in the geranylgeranylation of H-ras-CAIL proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50216999(CHEMBL3349357)
Affinity DataIC50:  200nMAssay Description:Inhibitory concentration was evaluated against Farnesyltransferase in the farnesylation of H-ras proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha(Bos taurus (bovine))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM50079806(2-[1-[4-amino-5-sulfanyl-(E,4R)-2-pentenyl]-4-(2-p...)
Affinity DataIC50:  210nMAssay Description:Inhibitory concentration was evaluated against Farnesyltransferase in the farnesylation of H-ras proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50079811(2-[1-[4-amino-5-sulfanyl-(E,4R)-2-pentenyl]-4-(4-i...)
Affinity DataIC50:  210nMAssay Description:In vitro inhibitory activity against Geranylgeranyl transferase in the geranylgeranylation of H-ras-CAIL proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50079804(2-[1-[4-amino-5-sulfanyl-(E,4R)-2-pentenyl]-4-(4-p...)
Affinity DataIC50:  250nMAssay Description:In vitro inhibitory activity against Geranylgeranyl transferase in the geranylgeranylation of H-ras-CAIL proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50079805(CHEMBL302834 | methyl 2-[1-[5-amino-6-sulfanyl-(5R...)
Affinity DataIC50:  350nMAssay Description:Inhibitory concentration against Farnesyltransferase for Farnesylation of H-ras protein InNIH 3T3 cells transformed with activated H-rasMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50059858((S)-2-((3Z,6E)-(2S,5S,8R)-8-Amino-2-benzyl-5-isopr...)
Affinity DataIC50:  370nMAssay Description:Inhibitory concentration against Farnesyltransferase for Farnesylation of H-ras protein InNIH 3T3 cells transformed with activated H-rasMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha(Bos taurus (bovine))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM50366603(CHEMBL1793799 | CHEMBL3349310)
Affinity DataIC50:  450nMAssay Description:Inhibitory concentration was evaluated against Farnesyltransferase in the farnesylation of H-ras proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50079785(CHEMBL433102 | methyl 2-[1-[5-amino-6-sulfanyl-(E,...)
Affinity DataIC50:  490nMAssay Description:Inhibitory concentration against Farnesyltransferase for Farnesylation of H-ras protein InNIH 3T3 cells transformed with activated H-rasMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50079793(2-[1-[5-amino-6-sulfanyl-(E,5R)-3-hexenyl]-4-pheno...)
Affinity DataIC50:  570nMAssay Description:In vitro inhibitory activity against Geranylgeranyl transferase in the geranylgeranylation of H-ras-CAIL proteinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50079790((S)-2-{[(2S,4S)-1-((E)-(2S,5R)-5-Amino-2-isopropyl...)
Affinity DataIC50:  840nMAssay Description:Inhibitory concentration against Farnesyltransferase for Farnesylation of H-ras protein InNIH 3T3 cells transformed with activated H-rasMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50079800(CHEMBL303363 | methyl 2-[1-[5-amino-6-sulfanyl-(5R...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against Farnesyltransferase for Farnesylation of H-ras protein InNIH 3T3 cells transformed with activated H-rasMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM50403702(CHEMBL39858)
Affinity DataIC50:  2.30E+3nMAssay Description:Multidrug-resistant reversal activity using P388/VMDRC.04 cells (a subline of P388 murine leukemia cells expressing human recombinant human P-glycopr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50079802(CHEMBL302025 | methyl 2-[1-[4-amino-5-sulfanyl-(E,...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibitory concentration against Farnesyltransferase for Farnesylation of H-ras protein InNIH 3T3 cells transformed with activated H-rasMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
Eisai Research Institute

Curated by ChEMBL
LigandPNGBDBM81939(CAS_52-53-9 | NSC_62969 | VERAPAMIL)
Affinity DataIC50:  3.10E+3nMAssay Description:Evaluated for cytotoxicity using P388/VMDRC.04 cells (a subline of P388 murine leukemia cells expressing human recombinant human P-glycoprotein) in t...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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