Reaction Details | |||
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Target | RAC-gamma serine/threonine-protein kinase | ||
Ligand | BDBM50528415 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_1905007 (CHEMBL4407365) | ||
IC50 | 0.100000±n/a nM | ||
Citation | Dong, X; Zhan, W; Zhao, M; Che, J; Dai, X; Wu, Y; Xu, L; Zhou, Y; Zhao, Y; Tian, T; Cheng, G; Jin, Z; Li, J; Shao, Y; He, Q; Yang, B; Weng, Q; Hu, Y Discovery of 3,4,6-Trisubstituted Piperidine Derivatives as Orally Active, Low hERG Blocking Akt Inhibitors via Conformational Restriction and Structure-Based Design. J Med Chem62:7264-7288 (2019) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
RAC-gamma serine/threonine-protein kinase | |||
Name: | RAC-gamma serine/threonine-protein kinase | ||
Synonyms: | AKT3 | AKT3_HUMAN | PKB gamma | PKBG | Protein kinase Akt-3 | Protein kinase B (Akt 3) | Protein kinase B, gamma | RAC-PK-gamma | RAC-gamma serine/threonine-protein kinase | STK-2 | Serine/threonine-protein kinase AKT | Serine/threonine-protein kinase AKT3 | ||
Type: | Enzyme | ||
Mol. Mass.: | 55769.36 | ||
Organism: | Homo sapiens (Human) | ||
Description: | n/a | ||
Residue: | 479 | ||
Sequence: |
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BDBM50528415 | |||
n/a | |||
Name | BDBM50528415 | ||
Synonyms: | CHEMBL4457064 | ||
Type | Small organic molecule | ||
Emp. Form. | C24H24Cl2F2N4O8 | ||
Mol. Mass. | 605.372 | ||
SMILES | O[C@H]([C@@H](O)C(O)=O)C(O)=O.Cn1ncc(Cl)c1-c1cc(oc1Cl)C(=O)N[C@@H]1CNCC[C@H]1c1ccc(F)c(F)c1 |r,wU:26.26,wD:1.0,2.2,31.33,(23.87,-52,;23.87,-53.52,;25.19,-54.29,;25.19,-55.81,;26.51,-53.52,;27.84,-54.29,;26.51,-52,;22.55,-54.29,;21.23,-53.52,;22.55,-55.81,;7.85,-50.48,;7.53,-51.98,;6.12,-52.61,;6.28,-54.14,;7.78,-54.46,;8.41,-55.87,;8.56,-53.13,;10.09,-52.98,;11.12,-54.12,;12.52,-53.5,;12.37,-51.97,;10.87,-51.64,;10.24,-50.24,;13.85,-54.28,;13.85,-55.82,;15.19,-53.51,;16.52,-54.28,;16.52,-55.82,;17.85,-56.59,;19.19,-55.83,;19.19,-54.28,;17.86,-53.51,;17.87,-51.98,;16.53,-51.21,;16.53,-49.66,;17.86,-48.89,;17.86,-47.35,;19.2,-49.66,;20.53,-48.88,;19.2,-51.21,)| | ||
Structure |