Compile Data Set for Download or QSAR
Found 127 with Last Name = 'lofgren' and Initial = 'ja'
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312752((S)-N1-(5-(isoquinolin-6-yl)-1,3,4-thiadiazol-2-yl...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312752((S)-N1-(5-(isoquinolin-6-yl)-1,3,4-thiadiazol-2-yl...)copy SMILEScopy InChI
Affinity DataIC50: 3.20nMAssay Description:Inhibition of human AKT1 in human U87MG cells assessed as PRAS40 phosphorylation after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312922((S)-N1-(5-(isoquinolin-6-yl)thiazol-2-yl)-3-(4-(tr...)copy SMILEScopy InChI
Affinity DataIC50: 4.90nMAssay Description:Inhibition of human AKT1 in human U87MG cells assessed as PRAS40 phosphorylation after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352815(CHEMBL1823655)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352823(CHEMBL1823663)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312934((S)-6-(2-(2-amino-3-(4-(trifluoromethyl)phenyl)pro...)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Inhibition of human AKT1 in human U87MG cells assessed as PRAS40 phosphorylation after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312931((S)-N1-(5-(1H-indazol-5-yl)thiazol-2-yl)-3-(4-(tri...)copy SMILEScopy InChI
Affinity DataIC50: 8.5nMAssay Description:Inhibition of human AKT1 in human U87MG cells assessed as PRAS40 phosphorylation after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312922((S)-N1-(5-(isoquinolin-6-yl)thiazol-2-yl)-3-(4-(tr...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Inhibition of CDK2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312942((S)-N1-(5-(3-aminoisoquinolin-6-yl)thiazol-2-yl)-3...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Inhibition of AKT1 after 10 mins by [gamma33]ATP assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312936((S)-6-(2-(2-amino-3-(4-(trifluoromethyl)phenyl)pro...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Inhibition of human AKT1 in human U87MG cells assessed as PRAS40 phosphorylation after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312942((S)-N1-(5-(3-aminoisoquinolin-6-yl)thiazol-2-yl)-3...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Inhibition of CDK2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312924((S)-N1-(3-(isoquinolin-6-yl)isoxazol-5-yl)-3-(4-(t...)copy SMILEScopy InChI
Affinity DataIC50: 17nMAssay Description:Inhibition of human AKT1 in human U87MG cells assessed as PRAS40 phosphorylation after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312933((S)-5-(2-(2-amino-3-(4-(trifluoromethyl)phenyl)pro...)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:Inhibition of human AKT1 in human U87MG cells assessed as PRAS40 phosphorylation after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352839(CHEMBL1823651)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352813(CHEMBL1823653)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352824(CHEMBL1823630)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312935((S)-6-(2-(2-amino-3-(4-(trifluoromethyl)phenyl)pro...)copy SMILEScopy InChI
Affinity DataIC50: 27nMAssay Description:Inhibition of human AKT1 in human U87MG cells assessed as PRAS40 phosphorylation after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352814(CHEMBL1823654)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312943((S)-N1-(5-(quinazolin-7-yl)thiazol-2-yl)-3-(4-(tri...)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:Inhibition of AKT1 after 10 mins by [gamma33]ATP assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352844(CHEMBL1823649)copy SMILEScopy InChI
Affinity DataIC50: 39nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312925((R)-4-(3-(isoquinolin-6-yl)isoxazol-5-yl)-1-(4-(tr...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of human AKT1 in human U87MG cells assessed as PRAS40 phosphorylation after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352837(CHEMBL1823643)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352835(CHEMBL1823641)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312752((S)-N1-(5-(isoquinolin-6-yl)-1,3,4-thiadiazol-2-yl...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Inhibition of CDK2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312752((S)-N1-(5-(isoquinolin-6-yl)-1,3,4-thiadiazol-2-yl...)copy SMILEScopy InChI
Affinity DataIC50: 53nMAssay Description:Inhibition of CDK2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312932((S)-N1-(5-(1-amino-1H-benzo[d][1,2,3]triazol-6-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 55nMAssay Description:Inhibition of CDK2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352833(CHEMBL1823639)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312932((S)-N1-(5-(1-amino-1H-benzo[d][1,2,3]triazol-6-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 77nMAssay Description:Inhibition of human AKT1 in human U87MG cells assessed as PRAS40 phosphorylation after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352832(CHEMBL1823638)copy SMILEScopy InChI
Affinity DataIC50: 80nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312941((S)-N1-(5-(isoquinolin-6-yl)-1,3,4-oxadiazol-2-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 85nMAssay Description:Inhibition of human AKT1 in human U87MG cells assessed as PRAS40 phosphorylation after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312924((S)-N1-(3-(isoquinolin-6-yl)isoxazol-5-yl)-3-(4-(t...)copy SMILEScopy InChI
Affinity DataIC50: 93nMAssay Description:Inhibition of CDK2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312940((S)-5-(2-(2-amino-3-(4-(trifluoromethyl)phenyl)pro...)copy SMILEScopy InChI
Affinity DataIC50: 95nMAssay Description:Inhibition of AKT1 after 10 mins by [gamma33]ATP assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352816(CHEMBL1823656)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetMast/stem cell growth factor receptor Kit(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312933((S)-5-(2-(2-amino-3-(4-(trifluoromethyl)phenyl)pro...)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibition of cKITMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312925((R)-4-(3-(isoquinolin-6-yl)isoxazol-5-yl)-1-(4-(tr...)copy SMILEScopy InChI
Affinity DataIC50: 117nMAssay Description:Inhibition of CDK2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352836(CHEMBL1823642)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312943((S)-N1-(5-(quinazolin-7-yl)thiazol-2-yl)-3-(4-(tri...)copy SMILEScopy InChI
Affinity DataIC50: 136nMAssay Description:Inhibition of CDK2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312934((S)-6-(2-(2-amino-3-(4-(trifluoromethyl)phenyl)pro...)copy SMILEScopy InChI
Affinity DataIC50: 138nMAssay Description:Inhibition of CDK2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352846(CHEMBL1823652)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352838(CHEMBL1823644)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312944((S)-N1-(5-(cinnolin-6-yl)thiazol-2-yl)-3-(4-(trifl...)copy SMILEScopy InChI
Affinity DataIC50: 141nMAssay Description:Inhibition of human AKT1 in human U87MG cells assessed as PRAS40 phosphorylation after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312933((S)-5-(2-(2-amino-3-(4-(trifluoromethyl)phenyl)pro...)copy SMILEScopy InChI
Affinity DataIC50: 185nMAssay Description:Inhibition of CDK2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352834(CHEMBL1823640)copy SMILEScopy InChI
Affinity DataIC50: 190nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352824(CHEMBL1823630)copy SMILEScopy InChI
Affinity DataIC50: 190nMAssay Description:Inhibition of CDK2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352831(CHEMBL1823637)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352815(CHEMBL1823655)copy SMILEScopy InChI
Affinity DataIC50: 240nMAssay Description:Inhibition of AKT1-mediated PRAS40 phosphorylation in human U87MG cells after 1 hr in presence of 5% FBS by ELISA assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352821(CHEMBL1823661)copy SMILEScopy InChI
Affinity DataIC50: 240nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312752((S)-N1-(5-(isoquinolin-6-yl)-1,3,4-thiadiazol-2-yl...)copy SMILEScopy InChI
Affinity DataIC50: 250nMAssay Description:Inhibition of human AKT1 in human U87MG cells assessed as PRAS40 phosphorylation after 1 hr by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50312933((S)-5-(2-(2-amino-3-(4-(trifluoromethyl)phenyl)pro...)copy SMILEScopy InChI
Affinity DataIC50: 250nMAssay Description:Inhibition of CDK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C4VWXPubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50352842(CHEMBL1823647)copy SMILEScopy InChI
Affinity DataIC50: 250nMAssay Description:Inhibition of AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0MNQPubMed
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