Compile Data Set for Download or QSAR
Found 71 with Last Name = 'elder' and Initial = 'jh'
TargetGag-Pol polyprotein [489-587,G537V,H558K,V571A](Human immunodeficiency virus)
The Scripps Research Institute

LigandPNGBDBM84460(HIV-1 PR Inhibitor, compound 6)copy SMILEScopy InChI
Affinity DataKi:  1.70nM IC50: 6nMAssay Description:The inhibition activity against HIV-1 PR and three mutants (G48V, V82F, V82A)were done in 96 well microtiter plate and were assayed. Wells that show...More data for this Ligand-Target Pair
Ligand InfoMMDBPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N21XCPubMedMMDB
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM84460(HIV-1 PR Inhibitor, compound 6)copy SMILEScopy InChI
Affinity DataKi:  2.70nMAssay Description:Inhibition of wild type HIV1 proteaseMore data for this Ligand-Target Pair
Ligand InfoMMDBPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2KZHPubMed
TargetGag-Pol polyprotein [489-587,G537V,H558K,V571A](Human immunodeficiency virus)
The Scripps Research Institute

LigandPNGBDBM84461(HIV-1 PR Inhibitor, compound 8)copy SMILEScopy InChI
Affinity DataKi:  4nM IC50: 13nMAssay Description:The inhibition activity against HIV-1 PR and three mutants (G48V, V82F, V82A)were done in 96 well microtiter plate and were assayed. Wells that show...More data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50200943(CHEMBL269769 | cyclopentyl (2S,3S)-3-[4-([4-(5-chl...)copy SMILEScopy InChI
Affinity DataKi:  8nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8MB6PubMed
TargetGag-Pol polyprotein [489-587,G537V,H558K,V571A](Human immunodeficiency virus)
The Scripps Research Institute

LigandPNGBDBM84461(HIV-1 PR Inhibitor, compound 8)copy SMILEScopy InChI
Affinity DataKi:  9.70nM IC50: 17nMAssay Description:The inhibition activity against HIV-1 PR and three mutants (G48V, V82F, V82A)were done in 96 well microtiter plate and were assayed. Wells that show...More data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587,G537V,H558K,V571A](Human immunodeficiency virus)
The Scripps Research Institute

LigandPNGBDBM84460(HIV-1 PR Inhibitor, compound 6)copy SMILEScopy InChI
Affinity DataKi:  10nM IC50: 19nMAssay Description:The inhibition activity against HIV-1 PR and three mutants (G48V, V82F, V82A)were done in 96 well microtiter plate and were assayed. Wells that show...More data for this Ligand-Target Pair
Ligand InfoMMDBPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N21XCPubMedMMDB
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50200945(CHEMBL262751 | cyclopentyl (2S,3S)-3-[4-([4-(2,5-d...)copy SMILEScopy InChI
Affinity DataKi:  10nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8MB6PubMed
TargetGag-Pol polyprotein [489-587,G537V,H558K,V571A](Human immunodeficiency virus)
The Scripps Research Institute

LigandPNGBDBM84461(HIV-1 PR Inhibitor, compound 8)copy SMILEScopy InChI
Affinity DataKi:  13nM IC50: 24nMAssay Description:The inhibition activity against HIV-1 PR and three mutants (G48V, V82F, V82A)were done in 96 well microtiter plate and were assayed. Wells that show...More data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50200956(CHEMBL262496 | cyclopentyl (2S,3S)-3-[4-([4-(2,5-d...)copy SMILEScopy InChI
Affinity DataKi:  14nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8MB6PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50200944(CHEMBL407802 | cyclopentyl (2S,3S)-3-(4-((4-(5-chl...)copy SMILEScopy InChI
Affinity DataKi:  21nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8MB6PubMed
TargetGag-Pol polyprotein [489-587,G537V,H558K,V571A](Human immunodeficiency virus)
The Scripps Research Institute

LigandPNGBDBM84460(HIV-1 PR Inhibitor, compound 6)copy SMILEScopy InChI
Affinity DataKi:  22nM IC50: 39nMAssay Description:The inhibition activity against HIV-1 PR and three mutants (G48V, V82F, V82A)were done in 96 well microtiter plate and were assayed. Wells that show...More data for this Ligand-Target Pair
Ligand InfoMMDBPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N21XCPubMedMMDB
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50200949(CHEMBL262738 | cyclopentyl (2S,3S)-3-[4-([4-(5-chl...)copy SMILEScopy InChI
Affinity DataKi:  23nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8MB6PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50200954(CHEMBL386849 | cyclopentyl (2S,3S)-3-[4-([4-(2,5-D...)copy SMILEScopy InChI
Affinity DataKi:  25nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8MB6PubMed
TargetGag-Pol polyprotein [489-587,G537V,H558K,V571A](Human immunodeficiency virus)
The Scripps Research Institute

LigandPNGBDBM84460(HIV-1 PR Inhibitor, compound 6)copy SMILEScopy InChI
Affinity DataKi:  27nM IC50: 46nMAssay Description:The inhibition activity against HIV-1 PR and three mutants (G48V, V82F, V82A)were done in 96 well microtiter plate and were assayed. Wells that show...More data for this Ligand-Target Pair
Ligand InfoMMDBPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N21XCPubMedMMDB
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50200951(CHEMBL267645 | cyclopentyl (2S,3S)-3-[4-([4-(2,5-d...)copy SMILEScopy InChI
Affinity DataKi:  27nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8MB6PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50200953(CHEMBL405393 | cyclopentyl (2S,3S)-3-(4-((4-(5-chl...)copy SMILEScopy InChI
Affinity DataKi:  28nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8MB6PubMed
TargetGag-Pol polyprotein [489-587,G537V,H558K,V571A](Human immunodeficiency virus)
The Scripps Research Institute

LigandPNGBDBM84461(HIV-1 PR Inhibitor, compound 8)copy SMILEScopy InChI
Affinity DataKi:  30nM IC50: 52nMAssay Description:The inhibition activity against HIV-1 PR and three mutants (G48V, V82F, V82A)were done in 96 well microtiter plate and were assayed. Wells that show...More data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50200948(CHEMBL386847 | cyclopentyl (2S,3S)-3-[4-([4-(2,5-d...)copy SMILEScopy InChI
Affinity DataKi:  32nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8MB6PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50200958(CHEMBL428624 | cyclopentyl (2S,3S)-3-[4-([4-(2,5-d...)copy SMILEScopy InChI
Affinity DataKi:  42nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8MB6PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50200950((R)-tetrahydrofuran-3-yl (2S,3S)-3-(4-((4-(5-chlor...)copy SMILEScopy InChI
Affinity DataKi:  83nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8MB6PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50200955(CHEMBL218359 | cyclopentyl (2S,3S)-5-methyl-1-phen...)copy SMILEScopy InChI
Affinity DataKi:  86nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8MB6PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50200946(CHEMBL385816 | cyclopentyl (2S,3S)-1,4-diphenyl-3-...)copy SMILEScopy InChI
Affinity DataKi:  98nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8MB6PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50200952(CHEMBL407996 | N-((2S,3S)-3-(4-((4-(5-chloro-2-met...)copy SMILEScopy InChI
Affinity DataKi: >2.50E+3nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8MB6PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50200947(CHEMBL405122 | cyclopentyl (2S,3S)-3-[4-([4-(2,5-d...)copy SMILEScopy InChI
Affinity DataKi: >2.50E+3nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8MB6PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50200957(CHEMBL216912 | [(1S,2S)-2-azido-1,2-dibenzylethyl]...)copy SMILEScopy InChI
Affinity DataKi:  3.10E+4nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8MB6PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096449((S)-2-[(R)-1-((1S,2R,3R,4S)-1-Benzyl-2,3-dihydroxy...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibitory concentration of the compound against TL3-resistant HIV(V82A) mutantMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM84460(HIV-1 PR Inhibitor, compound 6)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of wild type HIV1 proteaseMore data for this Ligand-Target Pair
Ligand InfoMMDBPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2KZHPubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096447((2R,3S)-3-{(S)-2-[(S)-2-Acetylamino-3-(4-hydroxy-p...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibitory concentration of the compound against drug-resistant HIV(G48V) mutant proteaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096451((2R,3S)-3-[(S)-2-((S)-2-Acetylamino-3-phenyl-propi...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibitory concentration of the compound against TL3-resistant HIV(L63P) mutant proteaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096445((2R,3S)-3-{(S)-2-[(S)-2-Acetylamino-3-(1H-indol-3-...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibitory concentration of the compound against TL3-resistant HIV(V771) mutantMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096445((2R,3S)-3-{(S)-2-[(S)-2-Acetylamino-3-(1H-indol-3-...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibitory concentration of the compound against TL3-resistant HIV(V82A) mutantMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096447((2R,3S)-3-{(S)-2-[(S)-2-Acetylamino-3-(4-hydroxy-p...)copy SMILEScopy InChI
Affinity DataIC50: 11nMAssay Description:Inhibitory concentration of the compound against drug-resistant HIV(G48V) mutantMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096451((2R,3S)-3-[(S)-2-((S)-2-Acetylamino-3-phenyl-propi...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Inhibitory concentration of the compound against TL3-resistant HIV(V82A) mutantMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096450((2R,3S)-2-Hydroxy-N-((8S,11S)-8-isopropyl-7,10-dio...)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Inhibitory concentration of the compound against human immunodeficiency virus (HIV) proteaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096452(CHEMBL430995 | [1-Benzyl-2-((8S,11S)-8-isopropyl-7...)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Inhibitory concentration of the compound against wild-type human immunodeficiency virus (HIV-WT) proteaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096449((S)-2-[(R)-1-((1S,2R,3R,4S)-1-Benzyl-2,3-dihydroxy...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Inhibitory concentration of the compound against human immunodeficiency virus (HIV) proteaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096449((S)-2-[(R)-1-((1S,2R,3R,4S)-1-Benzyl-2,3-dihydroxy...)copy SMILEScopy InChI
Affinity DataIC50: 16nMAssay Description:Inhibitory concentration of the compound against TL3-resistant HIV(L63P) mutantMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096449((S)-2-[(R)-1-((1S,2R,3R,4S)-1-Benzyl-2,3-dihydroxy...)copy SMILEScopy InChI
Affinity DataIC50: 21nMAssay Description:Inhibitory concentration of the compound against TL3-resistant HIV(L63P) mutant proteaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096447((2R,3S)-3-{(S)-2-[(S)-2-Acetylamino-3-(4-hydroxy-p...)copy SMILEScopy InChI
Affinity DataIC50: 26nMAssay Description:Inhibitory concentration of the compound against TL3-resistant HIV(F53L) mutant proteaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096445((2R,3S)-3-{(S)-2-[(S)-2-Acetylamino-3-(1H-indol-3-...)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibitory concentration of the compound against TL3-resistant HIV(L241) mutant proteaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096451((2R,3S)-3-[(S)-2-((S)-2-Acetylamino-3-phenyl-propi...)copy SMILEScopy InChI
Affinity DataIC50: 32nMAssay Description:Inhibitory concentration of the compound against drug-resistant HIV(V82F) mutantMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096445((2R,3S)-3-{(S)-2-[(S)-2-Acetylamino-3-(1H-indol-3-...)copy SMILEScopy InChI
Affinity DataIC50: 49nMAssay Description:Inhibitory concentration of the compound against TL3-resistant HIV(F53L) mutant proteaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096445((2R,3S)-3-{(S)-2-[(S)-2-Acetylamino-3-(1H-indol-3-...)copy SMILEScopy InChI
Affinity DataIC50: 49nMAssay Description:Inhibitory concentration of the compound against TL3-resistant HIV(M461) mutant proteaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096445((2R,3S)-3-{(S)-2-[(S)-2-Acetylamino-3-(1H-indol-3-...)copy SMILEScopy InChI
Affinity DataIC50: 49nMAssay Description:Inhibitory concentration of the compound against TL3-resistant HIV(L241) mutant proteaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096445((2R,3S)-3-{(S)-2-[(S)-2-Acetylamino-3-(1H-indol-3-...)copy SMILEScopy InChI
Affinity DataIC50: 49nMAssay Description:Inhibitory concentration of the compound against TL3-resistant HIV(V771) mutant proteaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096445((2R,3S)-3-{(S)-2-[(S)-2-Acetylamino-3-(1H-indol-3-...)copy SMILEScopy InChI
Affinity DataIC50: 49nMAssay Description:Inhibitory concentration of the compound against drug-resistant HIV(G48V) mutant proteaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096447((2R,3S)-3-{(S)-2-[(S)-2-Acetylamino-3-(4-hydroxy-p...)copy SMILEScopy InChI
Affinity DataIC50: 57nMAssay Description:Inhibitory concentration of the compound against drug-resistant HIV(V82F) mutant proteaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096447((2R,3S)-3-{(S)-2-[(S)-2-Acetylamino-3-(4-hydroxy-p...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Inhibitory concentration of the compound against TL3-resistant HIV(F53L) mutant proteaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096447((2R,3S)-3-{(S)-2-[(S)-2-Acetylamino-3-(4-hydroxy-p...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Inhibitory concentration of the compound against TL3-resistant HIV(L241) mutantMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50096447((2R,3S)-3-{(S)-2-[(S)-2-Acetylamino-3-(4-hydroxy-p...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Inhibitory concentration of the compound against human immunodeficiency virus (HIV) proteaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Q52NW4PubMed
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