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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase | ||
| Ligand | BDBM50598826 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_2228087 (CHEMBL5141600) | ||
| IC50 | 11±n/a nM | ||
| Citation |  Szychowski, J; Papp, R; Dietrich, E; Liu, B; Vallée, F; Leclaire, ME; Fourtounis, J; Martino, G; Perryman, AL; Pau, V; Yin, SY; Mader, P; Roulston, A; Truchon, JF; Marshall, CG; Diallo, M; Duffy, NM; Stocco, R; Godbout, C; Bonneau-Fortin, A; Kryczka, R; Bhaskaran, V; Mao, D; Orlicky, S; Beaulieu, P; Turcotte, P; Kurinov, I; Sicheri, F; Mamane, Y; Gallant, M; Black, WC Discovery of an Orally Bioavailable and Selective PKMYT1 Inhibitor, RP-6306. J Med Chem65:10251-10284 (2022) [PubMed] Article | ||
| More Info.: | Get all data from this article, Assay Method | ||
| Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase | |||
| Name: | Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase | ||
| Synonyms: | MYT1 | PKMYT1 | PMYT1_HUMAN | Tyrosine- and threonine-specific cdc2-inhibitory kinase | ||
| Type: | PROTEIN | ||
| Mol. Mass.: | 54523.76 | ||
| Organism: | Homo sapiens (Human) | ||
| Description: | ChEMBL_587209 | ||
| Residue: | 499 | ||
| Sequence: |
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| BDBM50598826 | |||
| n/a | |||
| Name | BDBM50598826 | ||
| Synonyms: | CHEMBL5184635 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C19H16N4O2 | ||
| Mol. Mass. | 332.3559 | ||
| SMILES | Cc1ccc(O)c(C)c1-n1cc(C(N)=O)c2nc3ccccc3nc12 |(2.67,-2.98,;2.96,-1.78,;4.44,-1.35,;4.8,.15,;3.69,1.21,;3.98,2.41,;2.21,.78,;1.32,1.63,;1.85,-.72,;.34,-1.04,;-.28,-2.45,;-1.81,-2.29,;-2.84,-3.43,;-4.05,-3.18,;-2.46,-4.61,;-2.13,-.78,;-3.47,-.01,;-3.47,1.53,;-4.8,2.3,;-4.8,3.84,;-3.47,4.61,;-2.13,3.84,;-2.13,2.3,;-.8,1.53,;-.8,-.01,)| | ||
| Structure | 
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