Reaction Details | |||
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Target | Tyrosine-protein kinase receptor UFO | ||
Ligand | BDBM531965 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | Cell-Free Axl Kinase Inhibitory Activity | ||
IC50 | 1.30±n/a nM | ||
Citation | Haginoya, N; Suzuki, T; Hayakawa, M; Ota, M; Tsukada, T; Kobayashi, K; Ando, Y; Jimbo, T; Nakamura, K Pyridone derivatives having tetrahydropyranylmethyl groups US Patent US11208403 Publication Date 12/28/2021 | ||
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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BDBM531965 | |||
n/a | |||
Name | BDBM531965 | ||
Synonyms: | US11208403, Example 42 | ||
Type | Small organic molecule | ||
Emp. Form. | C31H31FN4O4 | ||
Mol. Mass. | 542.6006 | ||
SMILES | COc1ccnc(N)c1-c1ccc(NC(=O)c2cn(CC3CCOCC3)cc(-c3ccc(C)cc3)c2=O)cc1F |(9.34,-.77,;8,-1.54,;8,-3.08,;9.34,-3.85,;9.34,-5.39,;8,-6.16,;6.67,-5.39,;5.33,-6.16,;6.67,-3.85,;5.33,-3.08,;4,-3.85,;2.67,-3.08,;2.67,-1.54,;1.33,-.77,;,-1.54,;,-3.08,;-1.33,-.77,;-1.33,.77,;-2.67,1.54,;-2.67,3.08,;-1.33,3.85,;,3.08,;1.33,3.85,;1.33,5.39,;,6.16,;-1.33,5.39,;-4,.77,;-4,-.77,;-5.33,-1.54,;-6.67,-.77,;-8,-1.54,;-8,-3.08,;-9.34,-3.85,;-6.67,-3.85,;-5.33,-3.08,;-2.67,-1.54,;-2.67,-3.08,;4,-.77,;5.33,-1.54,;6.67,-.77,)| | ||
Structure |