Reaction Details | |||
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Target | Tyrosine-protein kinase receptor UFO | ||
Ligand | BDBM50563646 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_2083406 (CHEMBL4739197) | ||
IC50 | 10.0±n/a nM | ||
Citation | Nissink, JWM; Bazzaz, S; Blackett, C; Clark, MA; Collingwood, O; Disch, JS; Gikunju, D; Goldberg, K; Guilinger, JP; Hardaker, E; Hennessy, EJ; Jetson, R; Keefe, AD; McCoull, W; McMurray, L; Olszewski, A; Overman, R; Pflug, A; Preston, M; Rawlins, PB; Rivers, E; Schimpl, M; Smith, P; Truman, C; Underwood, E; Warwicker, J; Winter-Holt, J; Woodcock, S; Zhang, Y Generating Selective Leads for Mer Kinase Inhibitors-Example of a Comprehensive Lead-Generation Strategy. J Med Chem64:3165-3184 (2021) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
Tyrosine-protein kinase receptor UFO | |||
Name: | Tyrosine-protein kinase receptor UFO | ||
Synonyms: | AXL | AXL oncogene | TEL/AXL | Tyrosine-protein kinase receptor UFO (AXL) | UFO | UFO_HUMAN | ||
Type: | Enzyme | ||
Mol. Mass.: | 98316.97 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P30530 | ||
Residue: | 894 | ||
Sequence: |
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BDBM50563646 | |||
n/a | |||
Name | BDBM50563646 | ||
Synonyms: | CHEMBL4740965 | ||
Type | Small organic molecule | ||
Emp. Form. | C20H19F3N6O2S | ||
Mol. Mass. | 464.464 | ||
SMILES | CNC(=O)c1sc(nc1C(F)(F)F)N1CC2CC1(CNC(=O)c1c[nH]c3ncccc13)C2 |(19.99,-20.98,;18.45,-20.98,;17.67,-22.31,;18.44,-23.64,;16.13,-22.3,;15.23,-21.05,;13.76,-21.53,;13.76,-23.06,;15.22,-23.55,;15.69,-25.01,;17.23,-25.01,;16.46,-26.34,;14.66,-26.15,;12.52,-20.62,;12.52,-19.08,;11.06,-18.59,;10.15,-19.84,;11.06,-21.09,;10.57,-22.55,;9.07,-22.86,;8.04,-21.72,;8.52,-20.25,;6.53,-22.03,;5.91,-23.42,;4.38,-23.26,;4.06,-21.76,;2.73,-21,;2.73,-19.45,;4.06,-18.68,;5.39,-19.45,;5.4,-21,;11.46,-20.07,)| | ||
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