Compile Data Set for Download or QSAR
Report error Found 32 Enz. Inhib. hit(s) with all data for entry = 3328
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31456BDBM31456(N-carbamimidoylglycyl deriv., 29b)
Affinity DataIC50: 1.20E+4nMT: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31430BDBM31430(Peptidomimetic, 5)
Affinity DataIC50: 1.60E+4nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31455BDBM31455(N-carbamimidoylglycyl deriv., 29a)
Affinity DataIC50: 1.70E+4nMT: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31446BDBM31446(phenylaminoethyl guanidine deriv., 21ci)
Affinity DataIC50: 1.70E+4nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31444BDBM31444(phenylaminoethyl guanidine deriv., 21bi)
Affinity DataIC50: 1.90E+4nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31443BDBM31443(phenylaminoethyl guanidine deriv., 21bh)
Affinity DataIC50: 2.30E+4nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31442BDBM31442(phenylaminoethyl guanidine deriv., 21bg)
Affinity DataIC50: 2.80E+4nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31427BDBM31427(Peptidomimetic, 2)
Affinity DataIC50: 2.80E+4nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31458BDBM31458(indole-aryl scaffold, 36b)
Affinity DataIC50: 3.20E+4nMT: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31445BDBM31445(phenylaminoethyl guanidine deriv., 21cg)
Affinity DataIC50: 3.80E+4nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31441BDBM31441(phenylaminoethyl guanidine deriv., 21bf)
Affinity DataIC50: 4.30E+4nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31452BDBM31452(phenylaminoethyl guanidine deriv., 22fa)
Affinity DataIC50: 4.40E+4nMT: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31428BDBM31428(Peptidomimetic, 3)
Affinity DataIC50: 5.00E+4nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31451BDBM31451(phenylaminoethyl guanidine deriv., 22ea)
Affinity DataIC50: 5.20E+4nMT: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31440BDBM31440(phenylaminoethyl guanidine deriv., 21be)
Affinity DataIC50: 5.50E+4nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31431BDBM31431(Peptidomimetic, 6)
Affinity DataIC50: 7.80E+4nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31450BDBM31450(phenylaminoethyl guanidine deriv., 22da)
Affinity DataIC50: 7.80E+4nMT: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31449BDBM31449(phenylaminoethyl guanidine deriv., 22ca)
Affinity DataIC50: 8.30E+4nMT: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31439BDBM31439(phenylaminoethyl guanidine deriv., 21bd)
Affinity DataIC50: 8.40E+4nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31436BDBM31436(phenylaminoethyl guanidine deriv., 21ba)
Affinity DataIC50: 8.40E+4nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31435BDBM31435(phenylaminoethyl guanidine deriv., 21aa)
Affinity DataIC50: 9.60E+4nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31453BDBM31453(quinazolin-7-yl, 15a)
Affinity DataIC50: 1.12E+5nMT: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31434BDBM31434(Peptidomimetic, 9)
Affinity DataIC50: 1.19E+5nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31457BDBM31457(indole-aryl scaffold, 36a)
Affinity DataIC50: 1.26E+5nMT: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31438BDBM31438(phenylaminoethyl guanidine deriv., 21bc)
Affinity DataIC50: 1.52E+5nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31448BDBM31448(phenylaminoethyl guanidine deriv., 22ba)
Affinity DataIC50: 1.58E+5nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31433BDBM31433(Peptidomimetic, 8)
Affinity DataIC50: 1.73E+5nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31437BDBM31437(phenylaminoethyl guanidine deriv., 21bb)
Affinity DataIC50: 2.15E+5nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31454BDBM31454(quinazolin-6-yl, 15b)
Affinity DataIC50: 2.32E+5nMT: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31447BDBM31447(phenylaminoethyl guanidine deriv., 22aa)
Affinity DataIC50: 2.53E+5nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31432BDBM31432(Peptidomimetic, 7)
Affinity DataIC50: 2.88E+5nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed
TargetRAC-alpha serine/threonine-protein kinase(Human)
Yale University

LigandChemical structure of BindingDB Monomer ID 31429BDBM31429(Peptidomimetic, 4)
Affinity DataIC50: 5.00E+5nMpH: 7.2 T: 2°CAssay Description:A bead-based FP assay methodology, termed IMAP, has been developed for the serine/threonine kinase, AKT that allows for direct measurement of product...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/13/2009
Entry Details Article
PubMed