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Found 115 with Last Name = 'blum' and Initial = 'cl'
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center

Curated by ChEMBL
LigandPNGBDBM50358043(CHEMBL1794051 | GW-5074)
Affinity DataIC50:  9nMAssay Description:Inhibitory concentration against raf kinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 11/12/13/14(Homo sapiens (Human))
Bayer Research Center

Curated by ChEMBL
LigandPNGBDBM50095423(5-tert-Butyl-3-(3-phenyl-ureido)-thiophene-2-carbo...)
Affinity DataIC50:  290nMAssay Description:Inhibition of Mitogen-activated protein kinase p38More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 11/12/13/14(Homo sapiens (Human))
Bayer Research Center

Curated by ChEMBL
LigandPNGBDBM50105619(1-(5-tert-Butyl-isoxazol-3-yl)-3-(4-phenoxy-phenyl...)
Affinity DataIC50:  360nMAssay Description:Inhibition of Escherichia coli derived Mitogen-activated protein kinase p38More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50290586(2-[9-Isopropyl-6-(4-methoxy-benzylamino)-9H-purin-...)
Affinity DataIC50:  500nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50113739(2(bis-(hydroxyethyl)amino)-6-(4-methoxybenzylamino...)
Affinity DataIC50:  500nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center

Curated by ChEMBL
LigandPNGBDBM50105619(1-(5-tert-Butyl-isoxazol-3-yl)-3-(4-phenoxy-phenyl...)
Affinity DataIC50:  540nMAssay Description:Inhibitory concentration against raf kinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50290560(2-[[6-(Biphenyl-4-ylamino)-9-isopropyl-9H-purin-2-...)
Affinity DataIC50:  600nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290593(3-{6-[(Biphenyl-4-ylmethyl)-amino]-9-isopropyl-9H-...)
Affinity DataIC50:  600nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290609(2-{(2-Hydroxy-ethyl)-[9-isopropyl-6-(4-thiophen-2-...)
Affinity DataIC50:  600nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290623(2-[{6-[(Benzo[1,3]dioxol-5-ylmethyl)-amino]-9-isop...)
Affinity DataIC50:  800nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290596(2-Amino-1-[9-isopropyl-6-(4-methoxy-benzylamino)-9...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290599((4-Chloro-benzyl)-(2-chloro-9-trifluoromethyl-9H-p...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50113740(2-{Benzyl-[9-isopropyl-6-(4-methoxy-benzylamino)-9...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290581(2-[[6-(4-Bromo-phenylamino)-9-isopropyl-9H-purin-2...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290602(3-{[9-Isopropyl-6-(4-methoxy-benzylamino)-9H-purin...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290611(2-[{6-[(Biphenyl-4-ylmethyl)-amino]-9-isopropyl-9H...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290613(2-[2-[Bis-(2-hydroxy-ethyl)-amino]-6-(4-methoxy-be...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290600(2-[9-Isopropyl-6-(4-methoxy-benzylamino)-9H-purin-...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center

Curated by ChEMBL
LigandPNGBDBM50105601(5-tert-Butyl-3-[3-(5-methyl-[1,3,4]thiadiazol-2-yl...)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibitory concentration against raf kinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50113727(2-[9-Isopropyl-6-(4-methoxy-benzylamino)-9H-purin-...)
Affinity DataIC50:  1.50E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center

Curated by ChEMBL
LigandPNGBDBM50095399(5-tert-Butyl-3-(3-p-tolyl-ureido)-thiophene-2-carb...)
Affinity DataIC50:  1.70E+3nMAssay Description:Inhibitory concentration against raf kinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center

Curated by ChEMBL
LigandPNGBDBM50105621(5-tert-Butyl-3-[3-(5-cyclopropyl-[1,3,4]thiadiazol...)
Affinity DataIC50:  1.90E+3nMAssay Description:Inhibitory concentration against raf kinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50290594(2-{(2-Hydroxy-ethyl)-[6-(4-methoxy-benzylamino)-9-...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center

Curated by ChEMBL
LigandPNGBDBM50105597(5-tert-Butyl-3-[3-(5-ethyl-[1,3,4]thiadiazol-2-yl)...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against raf kinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50113723(1-[9-Isopropyl-6-(4-methoxy-benzylamino)-9H-purin-...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290603(2-{(2-Hydroxy-ethyl)-[9-isobutyl-6-(4-methoxy-benz...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290563(2-[[6-(4-Bromo-benzylamino)-9-isopropyl-9H-purin-2...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50113694(3-[9-Isopropyl-6-(4-methoxy-benzylamino)-9H-purin-...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290618(2-[[9-Cyclopentyl-6-(4-methoxy-benzylamino)-9H-pur...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290566(2-[[6-(4-Butyl-benzylamino)-9-isopropyl-9H-purin-2...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290579(2-[(2-Hydroxy-ethyl)-(9-isopropyl-6-phenylamino-9H...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290567(2-[[6-(Cyclopropyl-methyl-amino)-9-isopropyl-9H-pu...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290610(2-[9-Isopropyl-6-(4-methoxy-benzylamino)-9H-purin-...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290614(2-{(2-Hydroxy-ethyl)-[6-(4-methoxy-benzylamino)-9-...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290589(2-{(2-Hydroxy-ethyl)-[6-(4-methoxy-benzylamino)-9-...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290573(2-{(2-Hydroxy-ethyl)-[9-isopropyl-6-(quinolin-3-yl...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290622(CHEMBL90860 | N*2*-[2-(1H-Indol-3-yl)-ethyl]-9-iso...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290590(2-[6-(4-Methoxy-benzylamino)-9-methyl-9H-purin-2-y...)
Affinity DataIC50:  2.50E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290564(1-{6-[(Biphenyl-4-ylmethyl)-amino]-9-isopropyl-9H-...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290607(4-(1-Hydroxy-2-{[9-isopropyl-6-(4-methoxy-benzylam...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center

Curated by ChEMBL
LigandPNGBDBM50095396(5-tert-Butyl-3-(3-p-tolyl-ureido)-furan-2-carboxyl...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibitory concentration against raf kinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50290561(2-{(2-Hydroxy-ethyl)-[6-(4-methoxy-benzylamino)-9-...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center

Curated by ChEMBL
LigandPNGBDBM50095428(5-tert-Butyl-3-(3-p-tolyl-ureido)-1H-pyrrole-2-car...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibitory concentration against raf kinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center

Curated by ChEMBL
LigandPNGBDBM50105606(5-tert-Butyl-3-[3-(4-methyl-thiophen-2-yl)-ureido]...)
Affinity DataIC50:  3.10E+3nMAssay Description:Inhibitory concentration against raf kinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center

Curated by ChEMBL
LigandPNGBDBM50105620(5-tert-Butyl-3-[3-(5-methyl-thiophen-2-yl)-ureido]...)
Affinity DataIC50:  3.70E+3nMAssay Description:Inhibitory concentration against raf kinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center

Curated by ChEMBL
LigandPNGBDBM50105612(5-Isopropyl-3-(3-p-tolyl-ureido)-thiophene-2-carbo...)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibitory concentration against raf kinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50290608(CHEMBL91378 | {1-[9-Isopropyl-6-(4-methoxy-benzyla...)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290571((2-Chloro-9-methyl-9H-purin-6-yl)-(4-methoxy-benzy...)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50290571((2-Chloro-9-methyl-9H-purin-6-yl)-(4-methoxy-benzy...)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibitory concentration against cyclin dependent kinase-2 (CDK2)/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Bayer Research Center

Curated by ChEMBL
LigandPNGBDBM50095403(1-(5-tert-butyl-2-(methylcarbamoyl)thiophen-3-yl)-...)
Affinity DataIC50:  4.90E+3nMAssay Description:Inhibitory concentration against raf kinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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