Compile Data Set for Download or QSAR
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Found 22 Enz. Inhib. hit(s) with all data for entry = 50012635
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121228(1-(2-{2-[3-(3H-Imidazol-4-yl)-2-(3-methyl-butyryla...)
Affinity DataIC50:  6.00E+3nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121238(1-(2-{2-[3-(3H-Imidazol-4-yl)-2-(3-methyl-butyryla...)
Affinity DataIC50:  9.00E+4nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121242(1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...)
Affinity DataIC50:  1.15E+5nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121227(1-(2-{2-[3-(3H-Imidazol-4-yl)-2-(3-methyl-butyryla...)
Affinity DataIC50:  1.65E+5nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121235(1-(2-{2-[2-(2-Amino-3-methyl-butyrylamino)-3-(3H-i...)
Affinity DataIC50:  2.60E+5nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121236(1-(2-{2-[2-Acetylamino-3-(3H-imidazol-4-yl)-propio...)
Affinity DataIC50:  2.80E+5nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121234(1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...)
Affinity DataIC50:  3.25E+5nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121233(1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...)
Affinity DataIC50:  3.65E+5nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121232(1-(2-{2-[3-(3H-Imidazol-4-yl)-2-(3-methyl-butyryla...)
Affinity DataIC50:  5.00E+5nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121226(1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...)
Affinity DataIC50:  6.80E+5nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121222(1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...)
Affinity DataIC50:  7.60E+5nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121240(1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...)
Affinity DataIC50:  8.20E+5nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121237(1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...)
Affinity DataIC50:  8.50E+5nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121225(1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...)
Affinity DataIC50:  9.70E+5nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121231(CHEMBL3085530 | N-{1-[1-[1-(2-{2-[1-(1-Carbamoyl-e...)
Affinity DataIC50:  1.00E+6nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121243(2-{[1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamin...)
Affinity DataIC50:  1.30E+6nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121239(1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...)
Affinity DataIC50:  1.50E+6nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121224(2-(2-{[1-(2-{2-[2-Amino-3-(3H-imidazol-4-yl)-propi...)
Affinity DataIC50:  2.00E+6nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedMMDB

TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121229(1-(2-{2-[2-(2-Amino-3-methyl-butyrylamino)-3-(3H-i...)
Affinity DataIC50:  2.10E+6nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121241(2-(2-Acetylamino-3-methyl-butyrylamino)-pentanedio...)
Affinity DataIC50:  2.50E+6nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121230(1-{2-[2-(3-3H-Imidazol-4-yl-propionylamino)-propio...)
Affinity DataIC50:  2.60E+6nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50121223(1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...)
Affinity DataIC50:  2.80E+6nMAssay Description:In vitro inhibition of human Cyclophillin A/protein interaction.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed