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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Ephrin type-B receptor 4 | ||
| Ligand | BDBM50157879 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_1570039 (CHEMBL3789402) | ||
| IC50 | >10000±n/a nM | ||
| Citation |  Stauffer, F; Cowan-Jacob, SW; Scheufler, C; Furet, P Identification of a 5-[3-phenyl-(2-cyclic-ether)-methylether]-4-aminopyrrolo[2,3-d]pyrimidine series of IGF-1R inhibitors. Bioorg Med Chem Lett26:2065-7 (2016) [PubMed] Article | ||
| More Info.: | Get all data from this article, Assay Method | ||
| Ephrin type-B receptor 4 | |||
| Name: | Ephrin type-B receptor 4 | ||
| Synonyms: | EPHB4 | EPHB4_HUMAN | Ephrin receptor | Ephrin type-B receptor 4 precursor (Tyrosine-protein kinase receptor HTK). | HTK | Hepatoma transmembrane kinase | MYK1 | TYRO11 | Tyrosine-protein kinase TYRO11 | VHL/Ephrin type-B receptor 4 | ||
| Type: | Enzyme | ||
| Mol. Mass.: | 108273.51 | ||
| Organism: | Homo sapiens (Human) | ||
| Description: | P54760 | ||
| Residue: | 987 | ||
| Sequence: |
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| BDBM50157879 | |||
| n/a | |||
| Name | BDBM50157879 | ||
| Synonyms: | CHEMBL1614712 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C27H29N5O | ||
| Mol. Mass. | 439.5521 | ||
| SMILES | [H][C@]1(CN2CCC2)C[C@]([H])(C1)n1cc(-c2cccc(OCc3ccccc3)c2)c2c(N)ncnc12 |wD:8.9,1.0,(6.47,-15.11,;5.71,-13.78,;4.93,-15.11,;5.69,-16.44,;5.68,-17.98,;7.22,-17.99,;7.23,-16.45,;5.31,-12.3,;6.81,-11.9,;6.02,-10.55,;7.2,-13.39,;7.59,-10.56,;6.61,-9.37,;7.45,-8.07,;7.04,-6.58,;5.56,-6.19,;5.15,-4.71,;6.24,-3.6,;7.73,-3.99,;8.81,-2.89,;10.15,-3.66,;11.48,-2.89,;12.81,-3.66,;14.12,-2.9,;14.13,-1.36,;12.8,-.59,;11.48,-1.36,;8.13,-5.47,;8.94,-8.47,;10.35,-7.7,;10.34,-6.15,;11.69,-8.46,;11.69,-10.01,;10.35,-10.79,;9.02,-10.01,)| | ||
| Structure | 
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