Reaction Details | |||
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Target | Tyrosine-protein kinase receptor UFO | ||
Ligand | BDBM50444273 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_1277931 (CHEMBL3094775) | ||
IC50 | 610±n/a nM | ||
Citation | Zhang, W; McIver, AL; Stashko, MA; DeRyckere, D; Branchford, BR; Hunter, D; Kireev, D; Miley, MJ; Norris-Drouin, J; Stewart, WM; Lee, M; Sather, S; Zhou, Y; Di Paola, JA; Machius, M; Janzen, WP; Earp, HS; Graham, DK; Frye, SV; Wang, X Discovery of Mer specific tyrosine kinase inhibitors for the treatment and prevention of thrombosis. J Med Chem56:9693-700 (2014) [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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BDBM50444273 | |||
n/a | |||
Name | BDBM50444273 | ||
Synonyms: | CHEMBL3093625 | ||
Type | Small organic molecule | ||
Emp. Form. | C24H34N6O5S | ||
Mol. Mass. | 518.629 | ||
SMILES | CCCNc1ncc(C(=O)Nc2ccc(cc2)S(=O)(=O)N2CCOCC2)c(N[C@H]2CC[C@H](O)CC2)n1 |r,wU:28.29,wD:31.33,(2.34,-21.85,;3.67,-22.62,;5,-21.85,;6.34,-22.62,;7.67,-21.85,;9.01,-22.62,;10.34,-21.85,;10.34,-20.3,;11.67,-19.52,;11.66,-17.98,;13,-20.29,;14.34,-19.51,;15.67,-20.29,;17,-19.51,;16.99,-17.97,;15.65,-17.21,;14.32,-17.98,;18.32,-17.19,;17.55,-15.85,;19.09,-15.85,;19.66,-17.96,;19.66,-19.49,;20.99,-20.25,;22.32,-19.48,;22.32,-17.94,;20.98,-17.17,;9,-19.54,;9,-18,;7.66,-17.23,;6.34,-18,;5,-17.23,;5,-15.69,;3.67,-14.91,;6.33,-14.92,;7.66,-15.68,;7.67,-20.31,)| | ||
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