Compile Data Set for Download or QSAR
Found 296 with Last Name = 'katritzky' and Initial = 'ar'
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM50404011(CHEMBL36900)copy SMILEScopy InChI
Affinity DataKi:  0.0100nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM164((4R,5R,6R)-4-benzyl-5-hydroxy-1,3-bis(1H-indazol-5...)copy SMILEScopy InChI
Affinity DataKi:  0.0200nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1150((4R,5R,6R)-Tetrahydro-1-(3-aminophenyl-methyl)-3-[...)copy SMILEScopy InChI
Affinity DataKi:  0.0200nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM50065089((4R,5R,6R)-Tetrahydro-1,3-bis[(3-benzamide oxime)-...)copy SMILEScopy InChI
Affinity DataKi:  0.0200nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM50404007(CHEMBL116517)copy SMILEScopy InChI
Affinity DataKi:  0.0200nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM50404010(CHEMBL324293)copy SMILEScopy InChI
Affinity DataKi:  0.0301nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1110((4R,5R,6R)-1,3-bis[(3-amino-1H-indazol-5-yl)methyl...)copy SMILEScopy InChI
Affinity DataKi:  0.0301nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM50404006(CHEMBL366576)copy SMILEScopy InChI
Affinity DataKi:  0.0601nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1108((4R,5R,6R)-4-benzyl-5-hydroxy-1,3-bis(1H-indazol-6...)copy SMILEScopy InChI
Affinity DataKi:  0.0601nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1149((4R,5R,6R)-Tetrahydro-1-(3-aminophenyl-methyl)-3-[...)copy SMILEScopy InChI
Affinity DataKi:  0.0601nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM50404005(CHEMBL113884)copy SMILEScopy InChI
Affinity DataKi:  0.0802nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1144((4R,5R,6R)-1-[(3-aminophenyl)methyl]-4-benzyl-5-hy...)copy SMILEScopy InChI
Affinity DataKi:  0.0802nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1080((4R,5R,6R)-Tetrahydro-1,3-bis[(3-benzamido)methyl]...)copy SMILEScopy InChI
Affinity DataKi:  0.0902nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1107((4R,5R,6R)-4-benzyl-5-hydroxy-6-(2-phenylethyl)-1,...)copy SMILEScopy InChI
Affinity DataKi:  0.100nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1148((4R,5R,6R)-1-[(3-amino-1H-indazol-5-yl)methyl]-3-[...)copy SMILEScopy InChI
Affinity DataKi:  0.100nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1109((4R,5R,6R)-4-benzyl-5-hydroxy-1,3-bis[(3-methyl-1H...)copy SMILEScopy InChI
Affinity DataKi:  0.100nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1145((4R,5R,6R)-1-[(3-aminophenyl)methyl]-6-benzyl-5-hy...)copy SMILEScopy InChI
Affinity DataKi:  0.100nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1146((4R,5R,6R)-1-[(3-aminophenyl)methyl]-6-benzyl-5-hy...)copy SMILEScopy InChI
Affinity DataKi:  0.130nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1102((4R,5R,6R)-Tetrahydro-1,3-bis[(3-carboxamidophenyl...)copy SMILEScopy InChI
Affinity DataKi:  0.150nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1131((4R,5R,6R)-Tetrahydro-1-(3-(N-hydroxycarboximidami...)copy SMILEScopy InChI
Affinity DataKi:  0.240nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1090((4R,5R,6R)-1,3-bis[(3-amino-4-fluorophenyl)methyl]...)copy SMILEScopy InChI
Affinity DataKi:  0.250nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1143((4R,5R,6R)-1-[(3-amino-1H-indazol-5-yl)methyl]-3,6...)copy SMILEScopy InChI
Affinity DataKi:  0.281nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1101((4R,5R,6R)-Tetrahydro-1,3-bis[(3-carboxamidophenyl...)copy SMILEScopy InChI
Affinity DataKi:  0.310nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1133((4R,5R,6R)-1-[(3-amino-1H-indazol-5-yl)methyl]-6-b...)copy SMILEScopy InChI
Affinity DataKi:  0.380nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1111((4R,5R,6R)-1,3-bis[(3-amino-1,2-benzoxazol-5-yl)me...)copy SMILEScopy InChI
Affinity DataKi:  0.410nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1141((4R,5R,6R)-Tetrahydro-1-(3-(N-hydroxycarboximidami...)copy SMILEScopy InChI
Affinity DataKi:  0.481nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1079((4R,5R,6R)-4-benzyl-5-hydroxy-1,3-bis({[3-(hydroxy...)copy SMILEScopy InChI
Affinity DataKi:  0.491nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1142((4R,5R,6R)-1-[(3-amino-1H-indazol-5-yl)methyl]-3,4...)copy SMILEScopy InChI
Affinity DataKi:  0.650nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1100((4R,5R,6R)-Tetrahydro-1,3-bis[(3-carboxyphenyl)met...)copy SMILEScopy InChI
Affinity DataKi:  0.871nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM50404008(CHEMBL286693)copy SMILEScopy InChI
Affinity DataKi:  0.912nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1136((4R,5R,6R)-6-benzyl-5-hydroxy-1-(1H-indazol-5-ylme...)copy SMILEScopy InChI
Affinity DataKi:  1.20nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1093((4R,5R,6R)-Tetrahydro-1,3-bis[(4-fluoro-3-benzamid...)copy SMILEScopy InChI
Affinity DataKi:  1.40nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1147((4R,5R,6R)-Tetrahydro-1-(3-aminophenyl-methyl)-3-[...)copy SMILEScopy InChI
Affinity DataKi:  1.60nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1091((4R,5R,6R)-1,3-bis[(3-aminophenyl)methyl]-4-benzyl...)copy SMILEScopy InChI
Affinity DataKi:  1.70nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1127((4R,5R,6R)-6-benzyl-5-hydroxy-1-[(3-hydroxyphenyl)...)copy SMILEScopy InChI
Affinity DataKi:  2.60nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetNeuronal acetylcholine receptor subunit alpha-4/beta-2(Rattus norvegicus (Rat))
University of Florida

Curated by ChEMBL
LigandPNGBDBM50320533(3-(4-Methylbenzylidene)anabaseine | CHEMBL1163379)copy SMILEScopy InChI
Affinity DataKi:  4nMAssay Description:Displacement of [3H]cytisine from alpha4beta2 nAChR in rat brain membrane after 3 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27081M9PubMed
TargetNeuronal acetylcholine receptor subunit alpha-4/beta-2(Rattus norvegicus (Rat))
University of Florida

Curated by ChEMBL
LigandPNGBDBM50320533(3-(4-Methylbenzylidene)anabaseine | CHEMBL1163379)copy SMILEScopy InChI
Affinity DataKi:  4nMAssay Description:Displacement of [3H]cytisine from alpha4beta2 nAChR in rat brain membrane after 3 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27081M9PubMed
TargetNeuronal acetylcholine receptor subunit alpha-7(Rattus norvegicus (Rat))
University of Florida

Curated by ChEMBL
LigandPNGBDBM50320547(3-(4-Difluoromethoxybenzylidene)anabaseine | CHEMB...)copy SMILEScopy InChI
Affinity DataKi:  4nMAssay Description:Displacement of [125I]-alpha-bungarotoxin from alpha7 nAChR in rat brain membrane after 3 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27081M9PubMed
TargetNeuronal acetylcholine receptor subunit alpha-7(Rattus norvegicus (Rat))
University of Florida

Curated by ChEMBL
LigandPNGBDBM50320547(3-(4-Difluoromethoxybenzylidene)anabaseine | CHEMB...)copy SMILEScopy InChI
Affinity DataKi:  4nMAssay Description:Displacement of [125I]-alpha-bungarotoxin from alpha7 nAChR in rat brain membrane after 3 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27081M9PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM50404009(CHEMBL420503)copy SMILEScopy InChI
Affinity DataKi:  4.90nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1129((4R,5R,6R)-Tetrahydro-1-(3-carboxamidophenylmethyl...)copy SMILEScopy InChI
Affinity DataKi:  5.60nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1128((4R,5R,6R)-1-[(3-aminophenyl)methyl]-6-benzyl-5-hy...)copy SMILEScopy InChI
Affinity DataKi:  6.20nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1094((4R,5R,6R)-1,3-bis[(4-amino-3-fluorophenyl)methyl]...)copy SMILEScopy InChI
Affinity DataKi:  8nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1076((4R,5R,6R)-Tetrahydro-1,3-bis[(3-cyanophenyl)methy...)copy SMILEScopy InChI
Affinity DataKi:  11nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetNeuronal acetylcholine receptor subunit alpha-4/beta-2(Rattus norvegicus (Rat))
University of Florida

Curated by ChEMBL
LigandPNGBDBM50320544(3-(3-(4-chlorobenzylidene)-3,4,5,6-tetrahydropyrid...)copy SMILEScopy InChI
Affinity DataKi:  13nMAssay Description:Displacement of [3H]cytisine from alpha4beta2 nAChR in rat brain membrane after 3 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27081M9PubMed
TargetNeuronal acetylcholine receptor subunit alpha-4/beta-2(Rattus norvegicus (Rat))
University of Florida

Curated by ChEMBL
LigandPNGBDBM50320544(3-(3-(4-chlorobenzylidene)-3,4,5,6-tetrahydropyrid...)copy SMILEScopy InChI
Affinity DataKi:  13nMAssay Description:Displacement of [3H]cytisine from alpha4beta2 nAChR in rat brain membrane after 3 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27081M9PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1130((4R,5R,6R)-Tetrahydro-1-(3-carboxamido-4-fluorophe...)copy SMILEScopy InChI
Affinity DataKi:  14nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1098((4R,5R,6R)-Tetrahydro-1,3-bis[(3-cyanophenyl)methy...)copy SMILEScopy InChI
Affinity DataKi:  14nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Florida

Curated by ChEMBL
LigandPNGBDBM1125((4R,5R,6R)-Tetrahydro-1-(3-cyanophenylmethyl)-6-ph...)copy SMILEScopy InChI
Affinity DataKi:  15nMAssay Description:Inhibitory activity of compound against HIV-1 aspartyl protease.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27WG3PubMed
TargetNeuronal acetylcholine receptor subunit alpha-4/beta-2(Rattus norvegicus (Rat))
University of Florida

Curated by ChEMBL
LigandPNGBDBM50320551(3-(4-Trifluoromethoxybenzylidene)anabaseine | CHEM...)copy SMILEScopy InChI
Affinity DataKi:  32nMAssay Description:Displacement of [3H]cytisine from alpha4beta2 nAChR in rat brain membrane after 3 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27081M9PubMed
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