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Found 32 with Last Name = 'moldes del carmen terán' and Initial = 'm'
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090867((2R,3S,4R,5R)-2-(aminomethyl)-5-(4-chloro-5-iodo-7...)
Affinity DataIC50:  0.100nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090843((1R,5S)-2-((3R,4aR)-4-Amino-5-bromo-pyrrolo[2,3-d]...)
Affinity DataIC50:  0.200nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090862((1R,5S)-2-((3R,4aR)-4-Amino-5-iodo-pyrrolo[2,3-d]p...)
Affinity DataIC50:  0.603nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090844((2R,3R,4S,5R)-2-(4-Chloro-5-iodo-pyrrolo[2,3-d]pyr...)
Affinity DataIC50:  3.02nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090854((2R,3S,4R,5R)-2-(azidomethyl)-5-(4-chloro-5-iodo-7...)
Affinity DataIC50:  8.91nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM14486((2R,3R,4S,5R)-2-(2-amino-9-iodo-3,5,7-triazabicycl...)
Affinity DataIC50:  8.91nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090853((2R,3R,4S,5R)-2-(4-Chloro-5-iodo-pyrrolo[2,3-d]pyr...)
Affinity DataIC50:  24nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50375654(CHEMBL99203 | US11633415, Compound 5-iodotubercidi...)
Affinity DataIC50:  25.7nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090863((2R,3R,4S,5R)-2-(4-Amino-5-iodo-pyrrolo[2,3-d]pyri...)
Affinity DataIC50:  34.7nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090847((2R,3R,4S,5R)-2-(4-Amino-5-bromo-pyrrolo[2,3-d]pyr...)
Affinity DataIC50:  39.8nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090855((2R,3R,4S,5R)-2-(5-Iodo-4-methylsulfanyl-pyrrolo[2...)
Affinity DataIC50:  44.7nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090852((2R,3R,4S,5R)-2-(5-Bromo-4-chloro-pyrrolo[2,3-d]py...)
Affinity DataIC50:  50.1nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090864((2R,3R,4S,5R)-2-(4-Amino-5-iodo-pyrrolo[2,3-d]pyri...)
Affinity DataIC50:  60.3nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090860((2R,3R,4S,5R)-2-(4-Amino-5-bromo-pyrrolo[2,3-d]pyr...)
Affinity DataIC50:  63.1nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090866((2R,3R,4S,5R)-2-(4-Chloro-5-methylsulfanyl-pyrrolo...)
Affinity DataIC50:  70.8nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090859((2R,3S,4R,5R)-2-(azidomethyl)-5-(5-bromo-4-chloro-...)
Affinity DataIC50:  100nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090837((2R,3R,4S,5R)-2-(4-Amino-5-iodo-pyrrolo[2,3-d]pyri...)
Affinity DataIC50:  100nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50000300((2R,3R,4S,5R)-2-(4-Amino-5-bromo-pyrrolo[2,3-d]pyr...)
Affinity DataIC50:  120nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090857((2R,3R,4S,5R)-2-(4-Amino-5-chloro-pyrrolo[2,3-d]py...)
Affinity DataIC50:  208nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090861(4-Amino-7-((2R,3R,4S,5R)-3,4-dihydroxy-5-methyl-te...)
Affinity DataIC50:  309nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50049823(4-Amino-7-((2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxyme...)
Affinity DataIC50:  309nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090838((2R,3R,4S,5R)-2-(4-Chloro-5-iodo-pyrrolo[2,3-d]pyr...)
Affinity DataIC50:  446nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090836(4-Amino-7-((2R,3R,4S,5R)-3,4-dihydroxy-5-methyl-te...)
Affinity DataIC50:  457nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50049820(4-Amino-5-carboxamide-7-(D-ribofuranosyl)pyrrolo[2...)
Affinity DataIC50:  467nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090856((2R,3R,4S,5R)-2-(4-Amino-5-bromo-pyrrolo[2,3-d]pyr...)
Affinity DataIC50:  501nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090840((2R,3R,4S,5R)-2-(4-Chloro-5-methyl-pyrrolo[2,3-d]p...)
Affinity DataIC50:  537nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090846(4-Amino-7-((2R,3R,4S,5R)-3,4-dihydroxy-5-methyl-te...)
Affinity DataIC50:  1.00E+3nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090865((2R,3R,4S,5R)-2-(4-Amino-5-iodo-pyrrolo[2,3-d]pyri...)
Affinity DataIC50:  1.20E+3nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090848((2R,3S,4R,5R)-2-(hydroxymethyl)-5-(5-iodo-4-(methy...)
Affinity DataIC50:  1.20E+3nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090841((2R,3R,4S,5R)-2-(4-Amino-5-methylsulfanyl-pyrrolo[...)
Affinity DataIC50:  1.35E+3nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090839((2R,3R,4S,5R)-2-(5-Iodo-4-mercapto-pyrrolo[2,3-d]p...)
Affinity DataIC50:  6.46E+3nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090851((2R,3R,4S,5R)-2-(4-Amino-5-methyl-pyrrolo[2,3-d]py...)
Affinity DataIC50:  1.66E+4nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed