Reaction Details |
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Target | Max-like protein X |
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Ligand | BDBM50388973 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_833604 (CHEMBL2066545) |
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Ki | 90±n/a nM |
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Citation | Flygare, JA; Beresini, M; Budha, N; Chan, H; Chan, IT; Cheeti, S; Cohen, F; Deshayes, K; Doerner, K; Eckhardt, SG; Elliott, LO; Feng, B; Franklin, MC; Reisner, SF; Gazzard, L; Halladay, J; Hymowitz, SG; La, H; LoRusso, P; Maurer, B; Murray, L; Plise, E; Quan, C; Stephan, JP; Young, SG; Tom, J; Tsui, V; Um, J; Varfolomeev, E; Vucic, D; Wagner, AJ; Wallweber, HJ; Wang, L; Ware, J; Wen, Z; Wong, H; Wong, JM; Wong, M; Wong, S; Yu, R; Zobel, K; Fairbrother, WJ Discovery of a potent small-molecule antagonist of inhibitor of apoptosis (IAP) proteins and clinical candidate for the treatment of cancer (GDC-0152). J Med Chem55:4101-13 (2012) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Max-like protein X |
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Name: | Max-like protein X |
Synonyms: | BHLHD13 | Class D basic helix-loop-helix protein 13 | MLX | MLX_HUMAN | Max-like bHLHZip protein | Protein BigMax | TCFL4 | Transcription factor-like protein 4 |
Type: | PROTEIN |
Mol. Mass.: | 33306.36 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_833604 |
Residue: | 298 |
Sequence: | MTEPGASPEDPWVKASPVGAHAGEGRAGRARARRGAGRRGASLLSPKSPTLSVPRGCRED
SSHPACAKVEYAYSDNSLDPGLFVESTRKGSVVSRANSIGSTSASSVPNTDDEDSDYHQE
AYKESYKDRRRRAHTQAEQKRRDAIKRGYDDLQTIVPTCQQQDFSIGSQKLSKAIVLQKT
IDYIQFLHKEKKKQEEEVSTLRKDVTALKIMKVNYEQIVKAHQDNPHEGEDQVSDQVKFN
VFQGIMDSLFQSFNASISVASFQELSACVFSWIEEHCKPQTLREIVIGVLHQLKNQLY
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BDBM50388973 |
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n/a |
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Name | BDBM50388973 |
Synonyms: | CHEMBL2063867 |
Type | Small organic molecule |
Emp. Form. | C24H35ClN4O3 |
Mol. Mass. | 463.013 |
SMILES | CN[C@@H](C)C(=O)N[C@@H](C1CCCCC1)C(=O)N1CCC[C@H]1C(=O)NCc1ccc(Cl)cc1 |r| |
Structure |
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