| Reaction Details |
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 | Report a problem with these data |
| Target | RAC-gamma serine/threonine-protein kinase |
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| Ligand | BDBM50606346 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_2254477 (CHEMBL5168687) |
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| IC50 | 0.100000±n/a nM |
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| Citation |  Ma, C; Wu, J; Wang, L; Ji, X; Wu, Y; Miao, L; Chen, D; Zhang, L; Wu, Y; Feng, H; Tang, Y; Zhou, Q; Pei, J; Yang, X; Xu, D; You, Q; Xie, Y Discovery of Clinical Candidate NTQ1062 as a Potent and Bioavailable Akt Inhibitor for the Treatment of Human Tumors. J Med Chem65:8144-8168 (2022) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| RAC-gamma serine/threonine-protein kinase |
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| Name: | RAC-gamma serine/threonine-protein kinase |
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| 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 |
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| Type: | Enzyme |
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| Mol. Mass.: | 55769.36 |
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| Organism: | Homo sapiens (Human) |
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| Description: | n/a |
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| Residue: | 479 |
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| Sequence: | MSDVTIVKEGWVQKRGEYIKNWRPRYFLLKTDGSFIGYKEKPQDVDLPYPLNNFSVAKCQ
LMKTERPKPNTFIIRCLQWTTVIERTFHVDTPEEREEWTEAIQAVADRLQRQEEERMNCS
PTSQIDNIGEEEMDASTTHHKRKTMNDFDYLKLLGKGTFGKVILVREKASGKYYAMKILK
KEVIIAKDEVAHTLTESRVLKNTRHPFLTSLKYSFQTKDRLCFVMEYVNGGELFFHLSRE
RVFSEDRTRFYGAEIVSALDYLHSGKIVYRDLKLENLMLDKDGHIKITDFGLCKEGITDA
ATMKTFCGTPEYLAPEVLEDNDYGRAVDWWGLGVVMYEMMCGRLPFYNQDHEKLFELILM
EDIKFPRTLSSDAKSLLSGLLIKDPNKRLGGGPDDAKEIMRHSFFSGVNWQDVYDKKLVP
PFKPQVTSETDTRYFDEEFTAQTITITPPEKYDEDGMDCMDNERRPHFPQFSYSASGRE
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| BDBM50606346 |
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| n/a |
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| Name | BDBM50606346 |
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| Synonyms: | CHEMBL5197007 | US20230321108, Isomer 4 of Example 3 |
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| Type | Small organic molecule |
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| Emp. Form. | C24H29ClN6O3 |
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| Mol. Mass. | 484.978 |
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| SMILES | [H][C@@]12C[C@]1([H])N(CCN2C(=O)[C@H](CNC(C)C)c1ccc(Cl)cc1)c1ncnc2NC(=O)O[C@@H](C)c12 |r| |
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| Structure | 
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