Compile Data Set for Download or QSAR
Report error Found 34 Enz. Inhib. hit(s) with all data for entry = 50006453
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049291BDBM50049291(2-{4-[(2-Methyl-4-oxo-3,4-dihydro-quinazolin-6-ylm...)
Affinity DataIC50: 10nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049286BDBM50049286(2-{4-[(2-Aminomethyl-4-oxo-3,4-dihydro-quinazolin-...)
Affinity DataIC50: 20nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049276BDBM50049276(2-(2-Fluoro-4-{methyl-[7-methyl-2-(4-methyl-pipera...)
Affinity DataIC50: 28nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50033910BDBM50033910(4-[(2,7-Dimethyl-4-oxo-3,4-dihydro-quinazolin-6-yl...)
Affinity DataIC50: 44nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50012244BDBM50012244(CHEMBL25889 | 2-{4-[(2-Methyl-4-oxo-3,4-dihydro-qu...)
Affinity DataIC50: 50nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049267BDBM50049267(4-[(2,7-Dimethyl-4-oxo-3,4-dihydro-quinazolin-6-yl...)
Affinity DataIC50: 56nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049288BDBM50049288(2-Fluoro-4-[(2-hydroxymethyl-7-methyl-4-oxo-3,4-di...)
Affinity DataIC50: 72nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049266BDBM50049266(2-Fluoro-4-[(2-hydroxymethyl-7-methyl-4-oxo-3,4-di...)
Affinity DataIC50: 80nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049281BDBM50049281(4-[(2-Dimethylaminomethyl-7-methyl-4-oxo-3,4-dihyd...)
Affinity DataIC50: 84nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049273BDBM50049273(2-{4-[(2-Hydroxymethyl-4-oxo-3,4-dihydro-quinazoli...)
Affinity DataIC50: 100nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049261BDBM50049261(2-Fluoro-4-[(7-methyl-2-morpholin-4-ylmethyl-4-oxo...)
Affinity DataIC50: 100nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049272BDBM50049272(2-Fluoro-4-{[7-methyl-2-(4-methyl-piperazin-1-ylme...)
Affinity DataIC50: 110nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50033932BDBM50033932(4-[(2-Methyl-4-oxo-3,4-dihydro-quinazolin-6-ylmeth...)
Affinity DataIC50: 110nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049283BDBM50049283(2-Fluoro-4-{[7-methyl-4-oxo-2-(pyrimidin-2-ylsulfa...)
Affinity DataIC50: 110nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049270BDBM50049270(4-[(2-Dimethylaminomethyl-7-methyl-4-oxo-3,4-dihyd...)
Affinity DataIC50: 140nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049269BDBM50049269(4-[(2-{[Bis-(2-hydroxy-ethyl)-amino]-methyl}-7-met...)
Affinity DataIC50: 160nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049279BDBM50049279(4-{[2-(Methanesulfonylamino-methyl)-4-oxo-3,4-dihy...)
Affinity DataIC50: 180nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049263BDBM50049263(4-[(2-{[(2-Dimethylamino-ethyl)-methyl-amino]-meth...)
Affinity DataIC50: 200nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049277BDBM50049277(2-(4-{[4-Oxo-2-(pyrimidin-2-ylsulfanylmethyl)-3,4-...)
Affinity DataIC50: 240nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049282BDBM50049282(4-[(2-Hydroxymethyl-4-oxo-3,4-dihydro-quinazolin-6...)
Affinity DataIC50: 300nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049280BDBM50049280(4-[(2-Cyanomethyl-4-oxo-3,4-dihydro-quinazolin-6-y...)
Affinity DataIC50: 380nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049290BDBM50049290(4-[(2-Morpholin-4-ylmethyl-4-oxo-3,4-dihydro-quina...)
Affinity DataIC50: 380nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049287BDBM50049287(N-(3-Nitro-benzyl)-4-{[4-oxo-2-(pyrimidin-2-ylsulf...)
Affinity DataIC50: 480nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049265BDBM50049265(4-{[2-(3-Hydroxy-pyrrolidin-1-ylmethyl)-4-oxo-3,4-...)
Affinity DataIC50: 600nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049274BDBM50049274(4-[(2-Dimethylaminomethyl-4-oxo-3,4-dihydro-quinaz...)
Affinity DataIC50: 620nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049271BDBM50049271(4-{[2-(2-Methoxy-ethoxymethyl)-4-oxo-3,4-dihydro-q...)
Affinity DataIC50: 640nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049289BDBM50049289(4-[(2-{[(2-Dimethylamino-ethyl)-methyl-amino]-meth...)
Affinity DataIC50: 820nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049284BDBM50049284(4-{[2-(4-Amino-pyrimidin-2-ylsulfanylmethyl)-4-oxo...)
Affinity DataIC50: 840nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049285BDBM50049285(4-{[2-(4-Methyl-piperazin-1-ylmethyl)-4-oxo-3,4-di...)
Affinity DataIC50: 900nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049275BDBM50049275(4-{[2-(4-Amino-6-hydroxy-pyrimidin-2-ylsulfanylmet...)
Affinity DataIC50: 1.04E+3nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049262BDBM50049262(4-[(2-Chloromethyl-4-oxo-3,4-dihydro-quinazolin-6-...)
Affinity DataIC50: 1.21E+3nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049268BDBM50049268(4-[(2-Aminomethyl-4-oxo-3,4-dihydro-quinazolin-6-y...)
Affinity DataIC50: 1.70E+3nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049278BDBM50049278(4-{[2-(4-Hydroxy-pyrimidin-2-ylsulfanylmethyl)-4-o...)
Affinity DataIC50: 3.30E+3nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetThymidylate synthase(Mouse)
Zeneca Pharma

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50049264BDBM50049264(4-[(2-Methylaminomethyl-4-oxo-3,4-dihydro-quinazol...)
Affinity DataIC50: 4.20E+3nMAssay Description:In vitro inhibitory activity against thymidylate synthase partially purified from L1210 mouse leukemia cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed