Compile Data Set for Download or QSAR
Found 132 with Last Name = 'allen' and Initial = 'ce'
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309191(2-Amino-N-(2-aminoethyl)-5-(2,3-dihydrothieno[3,4-...)copy SMILEScopy InChI
Affinity DataIC50: 28nMAssay Description:Inhibition of CHK2 by DELFIA assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309209(2-Amino-N-(2-aminoethyl)-5-(thiophen-3-yl)nicotina...)copy SMILEScopy InChI
Affinity DataIC50: 39nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309182(4-(2-Amino-5-(2,3-dihydrothieno[3,4-b][1,4]dioxin-...)copy SMILEScopy InChI
Affinity DataIC50: 92nMAssay Description:Inhibition of CHK2 by DELFIA assayMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50321650((4-(3-(1H-pyrazol-4-yl)imidazo[1,2-a]pyrazin-6-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Inhibition of CHK2 by DELFIA assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP5487PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309178(4-(2-Amino-5-(benzo[d][1,3]dioxol-4-yl)pyridin-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:Inhibition of CHK2 by DELFIA assayMore data for this Ligand-Target Pair
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50321650((4-(3-(1H-pyrazol-4-yl)imidazo[1,2-a]pyrazin-6-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 240nMAssay Description:Inhibition of ABL1 by Z-lite assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP5487PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309194(4-(2-Amino-5-(3,4-dimethoxyphenyl)pyridin-3-yl)ben...)copy SMILEScopy InChI
Affinity DataIC50: 270nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50321651((4-(3-(1H-pyrazol-4-yl)imidazo[1,2-a]pyrazin-6-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 300nMAssay Description:Inhibition of ABL1 by Z-lite assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP5487PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309206(4-(2-Amino-5-(4-hydroxy-3-methoxyphenyl)pyridin-3-...)copy SMILEScopy InChI
Affinity DataIC50: 310nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309184(4-(2-Amino-5-(thiophen-2-yl)pyridin-3-yl)benzamide...)copy SMILEScopy InChI
Affinity DataIC50: 350nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309187(2-Amino-N-(3-amino-3-oxopropyl)-5-(thiophen-3-yl)n...)copy SMILEScopy InChI
Affinity DataIC50: 410nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309186(4-(2-Amino-5-(3-(2-methoxyethoxy)phenyl)pyridin-3-...)copy SMILEScopy InChI
Affinity DataIC50: 420nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50321649(3,6-di(1H-pyrazol-4-yl)imidazo[1,2-a]pyrimidine | ...)copy SMILEScopy InChI
Affinity DataIC50: 440nMAssay Description:Inhibition of ABL1 by Z-lite assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP5487PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50321654(3-(1H-pyrazol-3-yl)-6-(1H-pyrazol-4-yl)imidazo[1,2...)copy SMILEScopy InChI
Affinity DataIC50: 480nMAssay Description:Inhibition of CHK2 by DELFIA assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP5487PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309210(4-(2-Amino-5-(3-methoxyphenyl)pyridin-3-yl)benzami...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309211(4-(2-Amino-5-(thiophen-3-yl)pyridin-3-yl)benzamide...)copy SMILEScopy InChI
Affinity DataIC50: 610nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309199(4-(2-Amino-5-(thiazol-5-yl)pyridin-3-yl)benzamide ...)copy SMILEScopy InChI
Affinity DataIC50: 680nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309190(2-AMINO-5-(2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-5-Y...)copy SMILEScopy InChI
Affinity DataIC50: 700nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
TargetRibosomal protein S6 kinase alpha-5(Homo sapiens (Human))
The Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50439463(CHEMBL2420911)copy SMILEScopy InChI
Affinity DataIC50: 700nMAssay Description:Inhibition of MSK1 (unknown origin) by microfluidic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2JK5PubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309209(2-Amino-N-(2-aminoethyl)-5-(thiophen-3-yl)nicotina...)copy SMILEScopy InChI
Affinity DataIC50: 780nMAssay Description:Inhibition of CHK1 by DELFIA assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309208(4-(2-Amino-5-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 830nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309207(4-(2-Amino-5-(thiazol-2-yl)pyridin-3-yl)benzamide ...)copy SMILEScopy InChI
Affinity DataIC50: 990nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309205(4-(2-Amino-5-(4-(2-methoxyethoxy)phenyl)pyridin-3-...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309204(4-(2-Amino-5-(thiazol-4-yl)pyridin-3-yl)benzamide ...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309206(4-(2-Amino-5-(4-hydroxy-3-methoxyphenyl)pyridin-3-...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of CHK1 by DELFIA assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase D2(Homo sapiens (Human))
The Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50439463(CHEMBL2420911)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of PKD2 (unknown origin) by microfluidic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2JK5PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50321655(3-(1H-indol-3-yl)-6-(1H-pyrazol-4-yl)imidazo[1,2-a...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of CHK2 by DELFIA assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP5487PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309203(4-(2-Amino-5-(benzo[d][1,3]dioxol-5-yl)pyridin-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 1.35E+3nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309202(4-(2-Amino-5-(4-methoxyphenyl)pyridin-3-yl)benzami...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50321654(3-(1H-pyrazol-3-yl)-6-(1H-pyrazol-4-yl)imidazo[1,2...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of CHK1 by DELFIAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP5487PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309201(4-(6-Amino-3,4'-bipyridin-5-yl)benzamide | CHEMBL5...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
The Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50439463(CHEMBL2420911)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of AKT1 (unknown origin) by microfluidic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2JK5PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50321656((3-(3-(1H-pyrazol-4-yl)imidazo[1,2-a]pyrazin-6-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of CHK2 by DELFIA assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP5487PubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50439463(CHEMBL2420911)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibition of CHK1 (unknown origin) by Z'-Lyte assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2JK5PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309200(4-(6-amino-6'-(3-(dimethylamino)propoxy)-3,3'-bipy...)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50321650((4-(3-(1H-pyrazol-4-yl)imidazo[1,2-a]pyrazin-6-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of CHK1 by DELFIAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP5487PubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309199(4-(2-Amino-5-(thiazol-5-yl)pyridin-3-yl)benzamide ...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of CHK1 by DELFIA assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM2579((2S,3R,4R,6R)-3-methoxy-2-methyl-4-(methylamino)-2...)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of CHK1 by DELFIA assayMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309198(4-(2-amino-5-(3-fluorophenyl)pyridin-3-yl)benzamid...)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309195(4-(6'-Amino-2,3'-bipyridin-5'-yl)benzamide | CHEMB...)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309196(4-(6-Amino-3,3'-bipyridin-5-yl)benzamide | CHEMBL6...)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309197(4-(2-Amino-5-(2,3-dihydrobenzo[b][1,4]dioxin-5-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50321651((4-(3-(1H-pyrazol-4-yl)imidazo[1,2-a]pyrazin-6-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of CHK2 by DELFIA assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP5487PubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309194(4-(2-Amino-5-(3,4-dimethoxyphenyl)pyridin-3-yl)ben...)copy SMILEScopy InChI
Affinity DataIC50: 2.30E+3nMAssay Description:Inhibition of CHK1 by DELFIA assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309193(4-(2-amino-5-(3,4,5-trimethoxyphenyl)pyridin-3-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 2.30E+3nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309192(4-(5-(3-acetamidophenyl)-2-aminopyridin-3-yl)benza...)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309190(2-AMINO-5-(2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-5-Y...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibition of CHK1 by DELFIA assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309191(2-Amino-N-(2-aminoethyl)-5-(2,3-dihydrothieno[3,4-...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibition of CHK1 by DELFIA assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309189(4-(2-amino-5-phenylpyridin-3-yl)benzamide | CHEMBL...)copy SMILEScopy InChI
Affinity DataIC50: 2.70E+3nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Institute of Cancer Research

Curated by ChEMBL
LigandPNGBDBM50309188(4-(2-amino-5-(3,4,5-trimethoxyphenyl)pyridin-3-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of CHK2 in human HT29 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974J2PubMed
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