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Report error Found 26 Enz. Inhib. hit(s) with all data for entry = 50035073
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM1866(3-(5-bromopyridin-2-yl)-1-[2-(pyridin-2-yl)ethyl]t...)
Affinity DataKi:  600nMAssay Description:Binding affinity against HIV reverse transcriptase (Estimated Ki)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50078263(1-(5-Bromo-pyridin-2-yl)-3-[2-(2-fluoro-phenyl)-et...)
Affinity DataKi:  600nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091963(1-(5-Bromo-pyridin-2-yl)-3-((R)-1-cyclohexyl-ethyl...)
Affinity DataKi:  1.10E+3nMAssay Description:Binding affinity against HIV reverse transcriptase (Estimated Ki)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091962(1-(5-Chloro-pyridin-2-yl)-3-((R)-1-cyclohexyl-ethy...)
Affinity DataKi:  1.20E+3nMAssay Description:Binding affinity against HIV reverse transcriptase (Estimated Ki)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091966(1-((R)-1-Cyclohexyl-ethyl)-3-thiazol-2-yl-thiourea...)
Affinity DataKi:  1.20E+4nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091972(1-(5-Bromo-pyridin-2-yl)-3-((S)-1-cyclohexyl-ethyl...)
Affinity DataKi: >1.00E+5nMAssay Description:Binding affinity against HIV reverse transcriptase (Estimated Ki)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091973(1-(5-Chloro-pyridin-2-yl)-3-((S)-1-cyclohexyl-ethy...)
Affinity DataKi: >1.00E+5nMAssay Description:Binding affinity against HIV reverse transcriptase (Estimated Ki)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091964(1-((S)-1-Cyclohexyl-ethyl)-3-pyridin-2-yl-thiourea...)
Affinity DataKi: >1.00E+5nMAssay Description:Binding affinity against HIV reverse transcriptase (Estimated Ki)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091970(1-((S)-1-Cyclohexyl-ethyl)-3-thiazol-2-yl-thiourea...)
Affinity DataKi: >1.00E+5nMAssay Description:Binding affinity against HIV reverse transcriptase (Estimated Ki)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091971(1-((R)-1-Cyclohexyl-ethyl)-3-pyridin-2-yl-thiourea...)
Affinity DataKi: >1.00E+5nMAssay Description:Binding affinity against HIV reverse transcriptase (Estimated Ki)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50078263(1-(5-Bromo-pyridin-2-yl)-3-[2-(2-fluoro-phenyl)-et...)
Affinity DataIC50:  600nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM1866(3-(5-bromopyridin-2-yl)-1-[2-(pyridin-2-yl)ethyl]t...)
Affinity DataIC50:  800nMAssay Description:Binding affinity against HIV reverse transcriptase (Estimated Ki)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091963(1-(5-Bromo-pyridin-2-yl)-3-((R)-1-cyclohexyl-ethyl...)
Affinity DataIC50:  1.20E+3nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091965(1-(5-Chloro-pyridin-2-yl)-3-((R)-1-phenyl-ethyl)-t...)
Affinity DataIC50:  1.20E+3nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091962(1-(5-Chloro-pyridin-2-yl)-3-((R)-1-cyclohexyl-ethy...)
Affinity DataIC50:  1.40E+3nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM1944(BHAP deriv. | CHEMBL593 | DELAVIRDINE MESYLATE | D...)
Affinity DataIC50:  1.50E+3nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank
MMDB
PDB3D3D Structure (crystal)

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091969(1-(5-Bromo-pyridin-2-yl)-3-((R)-1-phenyl-ethyl)-th...)
Affinity DataIC50:  1.60E+3nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091966(1-((R)-1-Cyclohexyl-ethyl)-3-thiazol-2-yl-thiourea...)
Affinity DataIC50:  1.30E+4nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM1434(11-cyclopropyl-5,11-dihydro-4-methyl-6H-dipyrido[3...)
Affinity DataIC50:  2.30E+4nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank
MMDB
PDB3D3D Structure (crystal)

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091973(1-(5-Chloro-pyridin-2-yl)-3-((S)-1-cyclohexyl-ethy...)
Affinity DataIC50: >1.00E+5nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091968(1-(5-Bromo-pyridin-2-yl)-3-((S)-1-phenyl-ethyl)-th...)
Affinity DataIC50: >1.00E+5nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091970(1-((S)-1-Cyclohexyl-ethyl)-3-thiazol-2-yl-thiourea...)
Affinity DataIC50: >1.00E+5nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091967(1-(5-Chloro-pyridin-2-yl)-3-((S)-1-phenyl-ethyl)-t...)
Affinity DataIC50: >1.00E+5nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091964(1-((S)-1-Cyclohexyl-ethyl)-3-pyridin-2-yl-thiourea...)
Affinity DataIC50: >1.00E+5nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091972(1-(5-Bromo-pyridin-2-yl)-3-((S)-1-cyclohexyl-ethyl...)
Affinity DataIC50: >1.00E+5nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Institute

Curated by ChEMBL
LigandPNGBDBM50091971(1-((R)-1-Cyclohexyl-ethyl)-3-pyridin-2-yl-thiourea...)
Affinity DataIC50: >1.00E+5nMAssay Description:Compound was evaluated for its inhibitory activity against recombinant HIV-1 Reverse transcriptase using cell free RT inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed