Reaction Details | |||
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Target | Tyrosine-protein kinase receptor UFO | ||
Ligand | BDBM50444242 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_1277931 (CHEMBL3094775) | ||
IC50 | 260±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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BDBM50444242 | |||
n/a | |||
Name | BDBM50444242 | ||
Synonyms: | CHEMBL3093755 | ||
Type | Small organic molecule | ||
Emp. Form. | C22H32N6O4S | ||
Mol. Mass. | 476.592 | ||
SMILES | CCCCNc1ncc(C(=O)NCc2ccc(cc2)S(N)(=O)=O)c(N[C@H]2CC[C@H](O)CC2)n1 |r,wU:25.25,wD:28.29,(24.27,-9.22,;25.6,-8.45,;26.93,-9.22,;28.27,-8.45,;29.6,-9.22,;30.94,-8.45,;32.27,-9.22,;33.61,-8.45,;33.6,-6.9,;34.93,-6.12,;34.93,-4.58,;36.27,-6.89,;37.6,-6.11,;38.94,-6.88,;38.94,-8.42,;40.27,-9.18,;41.6,-8.41,;41.59,-6.86,;40.26,-6.1,;42.94,-9.17,;44.27,-8.39,;43.7,-10.5,;42.17,-10.5,;32.27,-6.14,;32.26,-4.6,;30.93,-3.83,;29.59,-4.61,;28.25,-3.84,;28.25,-2.29,;26.92,-1.52,;29.59,-1.53,;30.92,-2.29,;30.94,-6.91,)| | ||
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