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Assay Detail

CHEMBL959245

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Binding
Inhibition of AKT2
24
Total Activities
13
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Intermediate

Target

RAC-beta serine/threonine-protein kinase (CHEMBL2431)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery of 5-pyrrolopyridinyl-2-thiophenecarboxamides as potent AKT kinase inhibitors.
Seefeld MA, Rouse MB, McNulty KC, Sun L, Wang J, Yamashita DS, Luengo JI, Zhang S, Minthorn EA, Concha NO, Heerding DA.
Bioorg Med Chem Lett (2009) 19 : 2244 -2248
PubMed 19285393 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 7.58 8.22
Ki 12 7.93 9.20

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL523586 2 9.20
CHEMBL496690 2 8.70
CHEMBL470597 2 8.52
CHEMBL520788 2 8.40
CHEMBL482536 2 8.40
CHEMBL470598 2 8.22
CHEMBL469590 2 8.10
CHEMBL498052 1 8.10
CHEMBL482537 2 7.80
CHEMBL524998 2 7.40
CHEMBL498051 1 7.40
CHEMBL512135 2 6.90
CHEMBL513728 2 6.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL523586 Ki = 0.63 nM 9.20
CHEMBL496690 Ki = 2.0 nM 8.70
CHEMBL470597 Ki = 3.0 nM 8.52
CHEMBL482536 Ki = 4.0 nM 8.40
CHEMBL520788 Ki = 4.0 nM 8.40
CHEMBL496690 IC50 = 6.0 nM 8.22
CHEMBL470598 Ki = 6.0 nM 8.22
CHEMBL498052 IC50 = 8.0 nM 8.10
CHEMBL469590 Ki = 8.0 nM 8.10
CHEMBL523586 IC50 = 9.0 nM 8.05
CHEMBL482536 IC50 = 10.0 nM 8.00
CHEMBL470597 IC50 = 10.0 nM 8.00
CHEMBL469590 IC50 = 13.0 nM 7.89
CHEMBL482537 Ki = 16.0 nM 7.80
CHEMBL520788 IC50 = 25.0 nM 7.60
CHEMBL470598 IC50 = 25.0 nM 7.60
CHEMBL498051 Ki = 40.0 nM 7.40
CHEMBL524998 Ki = 40.0 nM 7.40
CHEMBL524998 IC50 = 63.0 nM 7.20
CHEMBL482537 IC50 = 79.0 nM 7.10
CHEMBL512135 Ki = 125.0 nM 6.90
CHEMBL512135 IC50 = 125.0 nM 6.90
CHEMBL513728 IC50 = 500.0 nM 6.30
CHEMBL513728 Ki = 800.0 nM 6.10