Compile Data Set for Download or QSAR
Found 547 with Last Name = 'ternansky' and Initial = 'rj'
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, L.L.C.

Curated by ChEMBL
LigandPNGBDBM50121753(1-(5-Chloro-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidin...)copy SMILEScopy InChI
Affinity DataKi:  5nMAssay Description:Binding affinity towards recombinant thymidine phosphorylase TPMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GM87V9PubMed
TargetCaspase-3(Homo sapiens (Human))
Idun Pharmaceuticals, Inc.

Curated by ChEMBL
LigandPNGBDBM50133876((S)-3-{(S)-3-Methyl-2-[2-(naphthalen-1-yloxy)-acet...)copy SMILEScopy InChI
Affinity DataKi:  7.10nMAssay Description:Binding affinity of the compound was tested against caspase-3 (Csp-3)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21835WJPubMed
TargetCaspase-1(Mus musculus)
Idun Pharmaceuticals, Inc.

Curated by ChEMBL
LigandPNGBDBM50133876((S)-3-{(S)-3-Methyl-2-[2-(naphthalen-1-yloxy)-acet...)copy SMILEScopy InChI
Affinity DataKi:  70nMAssay Description:Binding affinity of the compound was tested against Murine caspase-1 (mCsp-1)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21835WJPubMed
TargetCaspase-3(Homo sapiens (Human))
Idun Pharmaceuticals, Inc.

Curated by ChEMBL
LigandPNGBDBM50133889((S)-3-{(S)-3-Methyl-2-[2-(naphthalen-1-yloxy)-acet...)copy SMILEScopy InChI
Affinity DataKi:  90nMAssay Description:Binding affinity of the compound was tested against caspase-3 (Csp-3)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21835WJPubMed
TargetCaspase-3(Homo sapiens (Human))
Idun Pharmaceuticals, Inc.

Curated by ChEMBL
LigandPNGBDBM50133879((S)-5-(Biphenyl-4-yloxy)-3-{(S)-3-methyl-2-[2-(nap...)copy SMILEScopy InChI
Affinity DataKi:  100nMAssay Description:Binding affinity of the compound was tested against caspase-3 (Csp-3)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21835WJPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, L.L.C.

Curated by ChEMBL
LigandPNGBDBM50201010(((2R,3aR,4R,6R,6aR)-4-(hydroxymethyl)-6-(5-methyl-...)copy SMILEScopy InChI
Affinity DataKi:  236nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FB52KFPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, L.L.C.

Curated by ChEMBL
LigandPNGBDBM50201013(((2S,3aR,4S,6R,6aR)-4-(hydroxymethyl)-6-(5-methyl-...)copy SMILEScopy InChI
Affinity DataKi:  1.05E+3nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FB52KFPubMed
TargetCaspase-1(Mus musculus)
Idun Pharmaceuticals, Inc.

Curated by ChEMBL
LigandPNGBDBM50133879((S)-5-(Biphenyl-4-yloxy)-3-{(S)-3-methyl-2-[2-(nap...)copy SMILEScopy InChI
Affinity DataKi:  2.68E+3nMAssay Description:Binding affinity of the compound was tested against Murine caspase-1 (mCsp-1)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21835WJPubMed
TargetCaspase-1(Mus musculus)
Idun Pharmaceuticals, Inc.

Curated by ChEMBL
LigandPNGBDBM50133889((S)-3-{(S)-3-Methyl-2-[2-(naphthalen-1-yloxy)-acet...)copy SMILEScopy InChI
Affinity DataKi:  3.17E+3nMAssay Description:Binding affinity of the compound was tested against Murine caspase-1 (mCsp-1)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21835WJPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, L.L.C.

Curated by ChEMBL
LigandPNGBDBM50201015(((2R,3aR,4R,6R,6aS)-6-(hydroxymethyl)-4-(5-methyl-...)copy SMILEScopy InChI
Affinity DataKi:  8.03E+3nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FB52KFPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, L.L.C.

Curated by ChEMBL
LigandPNGBDBM50201012(((2R,3aR,4S,6R,6aR)-4-(hydroxymethyl)-6-(5-methyl-...)copy SMILEScopy InChI
Affinity DataKi:  3.34E+4nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FB52KFPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, L.L.C.

Curated by ChEMBL
LigandPNGBDBM50201011(2-((2R,3aR,4R,6R,6aR)-4-(hydroxymethyl)-6-(5-methy...)copy SMILEScopy InChI
Affinity DataKi:  4.35E+4nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FB52KFPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, L.L.C.

Curated by ChEMBL
LigandPNGBDBM50121756((benzylamino)[(2,4-dioxo-1,2,3,4-tetrahydrothieno[...)copy SMILEScopy InChI
Affinity DataKi:  6.43E+4nMAssay Description:Binding affinity towards recombinant thymidine phosphorylase TPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GM87V9PubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, L.L.C.

Curated by ChEMBL
LigandPNGBDBM50121754(CHEMBL12488 | amino[(2,4-dioxo-1,2,3,4-tetrahydrot...)copy SMILEScopy InChI
Affinity DataKi:  7.60E+4nMAssay Description:Binding affinity towards recombinant thymidine phosphorylase TPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GM87V9PubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, L.L.C.

Curated by ChEMBL
LigandPNGBDBM50121757(6-Amino-1H-thieno[3,2-d]pyrimidine-2,4-dione | CHE...)copy SMILEScopy InChI
Affinity DataKi: >3.00E+5nMAssay Description:Binding affinity towards recombinant thymidine phosphorylase TPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GM87V9PubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, L.L.C.

Curated by ChEMBL
LigandPNGBDBM50201014(((2S,3aR,4R,6R,6aS)-6-(hydroxymethyl)-4-(5-methyl-...)copy SMILEScopy InChI
Affinity DataKi: >5.00E+5nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FB52KFPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, L.L.C.

Curated by ChEMBL
LigandPNGBDBM50121755(7-Amino-1H-thieno[3,2-d]pyrimidine-2,4-dione | CHE...)copy SMILEScopy InChI
Affinity DataKi: >6.00E+5nMAssay Description:Binding affinity towards recombinant thymidine phosphorylase TPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GM87V9PubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, L.L.C.

Curated by ChEMBL
LigandPNGBDBM50121758(CHEMBL274649 | amino[(2,4-dioxo-1,2,3,4-tetrahydro...)copy SMILEScopy InChI
Affinity DataKi: >2.40E+6nMAssay Description:Binding affinity towards recombinant thymidine phosphorylase TPMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2GM87V9PubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2156(1-(5-chloropyridin-2-yl)-3-[2-(1,3-dioxo-2,3-dihyd...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM1890(3-(5-bromopyridin-2-yl)-1-[2-(2,6-difluorophenyl)e...)copy SMILEScopy InChI
Affinity DataIC50: 1nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetCaspase-8(Homo sapiens (Human))TBA
LigandPNGBDBM572147(US11447497, Example 4)copy SMILES
Affinity DataIC50: 1nMAssay Description:Caspase-1 was diluted to 10 U/μl in assay buffer consisting of 50 mM HEPES, pH 7.4, 100 mM NaCl, 0.1% CHAPS, 1 mM EDTA, 10% glycerol and 10 mM D...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23X89W8US Patent
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2139(1-(5-chloropyridin-2-yl)-3-[2-(2-fluoro-3,6-dimeth...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2132(1-(5-bromopyridin-2-yl)-3-[2-(2-cyano-6-fluoro-3-m...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2142(1-(5-bromopyridin-2-yl)-3-[2-(6-chloro-3-ethoxy-2-...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2131(1-(5-bromopyridin-2-yl)-3-[2-(2-cyano-3-ethoxy-6-f...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetCaspase-1(Homo sapiens (Human))TBA
LigandPNGBDBM572147(US11447497, Example 4)copy SMILES
Affinity DataIC50: 2nMAssay Description:Caspase-1 was diluted to 10 U/μl in assay buffer consisting of 50 mM HEPES, pH 7.4, 100 mM NaCl, 0.1% CHAPS, 1 mM EDTA, 10% glycerol and 10 mM D...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23X89W8US Patent
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2143(1-(5-chloropyridin-2-yl)-3-[2-(2,4,6-trifluorophen...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2159(1-(5-chloropyridin-2-yl)-3-[2-(4,7-dichloro-1,3-di...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetCaspase-3(Homo sapiens (Human))
Idun Pharmaceuticals, Inc.

Curated by ChEMBL
LigandPNGBDBM50119218(4-Benzyloxycarbonylamino-4-[1-(2-hydroxy-5-oxo-tet...)copy SMILEScopy InChI
Affinity DataIC50: 2.30nMAssay Description:Inhibitory concentration of compound required against Caspase-3 compared to acylated dipeptidesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q289157SPubMed
TargetCaspase-3(Homo sapiens (Human))
Idun Pharmaceuticals, Inc.

Curated by ChEMBL
LigandPNGBDBM50119218(4-Benzyloxycarbonylamino-4-[1-(2-hydroxy-5-oxo-tet...)copy SMILEScopy InChI
Affinity DataIC50: 2.30nMAssay Description:Inhibitory concentration of compound required against Caspase-3 enzyme compared to acylated dipeptidesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24M93VXPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2153(3-[2-(2H-1,2,3-benzotriazol-2-yl)ethyl]-1-(5-bromo...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2133(3-[2-(2-cyano-6-fluoro-3-methoxyphenyl)ethyl]-1-(5...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2138(1-(5-bromopyridin-2-yl)-3-[2-(2,3-difluoro-6-metho...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetCaspase-3(Homo sapiens (Human))
Idun Pharmaceuticals, Inc.

Curated by ChEMBL
LigandPNGBDBM50119245(4-(2-Acetylamino-2-carboxy-acetylamino)-4-[1-(2-hy...)copy SMILEScopy InChI
Affinity DataIC50: 3.5nMAssay Description:Inhibitory concentration of compound required against Caspase-3 compared to acylated dipeptidesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q289157SPubMed
TargetCaspase-3(Homo sapiens (Human))
Idun Pharmaceuticals, Inc.

Curated by ChEMBL
LigandPNGBDBM50072047(4-(2-Acetylamino-3-carboxy-propionylamino)-4-[1-((...)copy SMILEScopy InChI
Affinity DataIC50: 3.5nMAssay Description:Inhibitory concentration of compound required against Caspase-3 enzyme compared to acylated dipeptidesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24M93VXPubMed
TargetCaspase-6(Homo sapiens (Human))
Idun Pharmaceuticals, Inc.

Curated by ChEMBL
LigandPNGBDBM50119267(4-[1-(2-Hydroxy-5-oxo-tetrahydro-furan-3-ylcarbamo...)copy SMILEScopy InChI
Affinity DataIC50: 3.5nMAssay Description:Inhibition of Caspase-6More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24M93VXPubMed
TargetCaspase-3(Homo sapiens (Human))
Idun Pharmaceuticals, Inc.

Curated by ChEMBL
LigandPNGBDBM50119267(4-[1-(2-Hydroxy-5-oxo-tetrahydro-furan-3-ylcarbamo...)copy SMILEScopy InChI
Affinity DataIC50: 3.80nMAssay Description:Inhibition of Caspase-3More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24M93VXPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2149(1-(5-chloropyridin-2-yl)-3-[2-(3-fluorofuran-2-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2124(1-(5-bromopyridin-2-yl)-3-[2-(3-ethoxy-2,6-difluor...)copy SMILEScopy InChI
Affinity DataIC50: 4nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetCaspase-1(Homo sapiens (Human))TBA
LigandPNGBDBM572145(US11447497, Example 2)copy SMILES
Affinity DataIC50: 4nMAssay Description:Caspase-1 was diluted to 10 U/μl in assay buffer consisting of 50 mM HEPES, pH 7.4, 100 mM NaCl, 0.1% CHAPS, 1 mM EDTA, 10% glycerol and 10 mM D...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23X89W8US Patent
TargetGag-Pol polyprotein [588-1127,Y768C]/[588-1147,Y768C](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2138(1-(5-bromopyridin-2-yl)-3-[2-(2,3-difluoro-6-metho...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2125(1-(5-bromopyridin-2-yl)-3-{2-[2,6-difluoro-3-(meth...)copy SMILEScopy InChI
Affinity DataIC50: 4nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2128(3-[2-(2-chloro-3-ethoxy-6-fluorophenyl)ethyl]-1-(5...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2129(1-(4-chloro-1,2-dihydropyridazin-1-yl)-3-[2-(2-chl...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2140(1-(5-chloropyridin-2-yl)-3-[2-(3-ethoxy-2-fluoro-6...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2135(1-(5-chloropyridin-2-yl)-3-[2-(2,5-dimethoxyphenyl...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2137(1-(5-bromopyridin-2-yl)-3-[2-(6-ethoxy-2,3-difluor...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2134(1-(4-chloro-1,2-dihydropyridazin-1-yl)-3-[2-(2-cya...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM2157(3-[2-(2-chloro-3-ethoxy-6-fluorophenyl)ethyl]-1-(5...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Lilly Research Laboratories

LigandPNGBDBM1893(3-(5-bromopyridin-2-yl)-1-[2-(2-ethoxy-6-fluorophe...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2542KSNPubMed
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