Compile Data Set for Download or QSAR
Report error Found 32 Enz. Inhib. hit(s) with all data for entry = 50041072
TargetAdenosine kinase(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 Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090843((2R,3R,4S,5R)-2-(4-amino-5-bromo-7H-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 Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090844(2-(4-Chloro-5-iodo-pyrrolo[2,3-d]pyrimidin-7-yl)-5...)
Affinity DataIC50: 3.02nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM14486(CHEMBL66280 | 5-Iodo-5-deoxytubercidin | 7-(5-deox...)
Affinity DataIC50: 8.91nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090854((2R,3S,4R,5R)-2-Azidomethyl-5-(4-chloro-5-iodo-pyr...)
Affinity DataIC50: 8.91nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090853(2-(4-Chloro-5-iodo-pyrrolo[2,3-d]pyrimidin-7-yl)-5...)
Affinity DataIC50: 24nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090863((2R,3R,4S,5R)-2-(4-amino-5-iodo-7H-pyrrolo[2,3-d]p...)
Affinity DataIC50: 34.7nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090847(2-(4-Amino-5-bromo-pyrrolo[2,3-d]pyrimidin-7-yl)-5...)
Affinity DataIC50: 39.8nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090855(2-(5-Iodo-4-methylsulfanyl-pyrrolo[2,3-d]pyrimidin...)
Affinity DataIC50: 44.7nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090860(2-(4-Amino-5-bromo-pyrrolo[2,3-d]pyrimidin-7-yl)-5...)
Affinity DataIC50: 63.1nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090866(2-(4-Chloro-5-methylsulfanyl-pyrrolo[2,3-d]pyrimid...)
Affinity DataIC50: 70.8nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090859(2-Azidomethyl-5-(5-bromo-4-chloro-pyrrolo[2,3-d]py...)
Affinity DataIC50: 100nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090837((2R,3R,4S,5R)-2-(4-amino-5-iodo-7H-pyrrolo[2,3-d]p...)
Affinity DataIC50: 100nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50000300(2-(4-Amino-5-bromo-pyrrolo[2,3-d]pyrimidin-7-yl)-5...)
Affinity DataIC50: 120nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090857(2-(4-Amino-5-chloro-pyrrolo[2,3-d]pyrimidin-7-yl)-...)
Affinity DataIC50: 208nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50049823(cid_247955 | 4-Amino-7-(3,4-dihydroxy-5-hydroxymet...)
Affinity DataIC50: 309nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50049820(cid_5153 | 4-Amino-7-(3,4-dihydroxy-5-hydroxymethy...)
Affinity DataIC50: 467nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090856((2R,3R,4S,5R)-2-(4-amino-5-bromo-7H-pyrrolo[2,3-d]...)
Affinity DataIC50: 501nMAssay Description:Concentration required for 50% inhibition of the adenosine kinase (AK) activity.More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090846(ethyl 4-amino-7-((2R,3R,4S,5R)-3,4-dihydroxy-5-met...)
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 Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090865((2R,3R,4S,5R)-2-(4-amino-5-iodo-7H-pyrrolo[2,3-d]p...)
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 Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090848((2R,3S,4R,5R)-2-Hydroxymethyl-5-(5-iodo-4-methylam...)
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 Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Vigo University

Curated by ChEMBL
LigandPNGBDBM50090839((2R,3R,4S,5R)-2-(5-iodo-4-mercapto-7H-pyrrolo[2,3-...)
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 Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
5/19/2013
Entry Details Article
PubMed