Reaction Details | |||
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Report a problem with these data | |||
Target | Fibroblast growth factor receptor 3 | ||
Ligand | BDBM102501 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | Kinase Assay | ||
IC50 | 530±0.0 nM | ||
Citation | Furet, P; Graus Porta, D; Guagnano, V Quinoxaline carboxamide derivatives as protein tyrosine kinase inhibitors US Patent US8536175 Publication Date 9/17/2013 | ||
More Info.: | Get all data from this article, Assay Method | ||
Fibroblast growth factor receptor 3 | |||
Name: | Fibroblast growth factor receptor 3 | ||
Synonyms: | CD_antigen: CD333 | FGFR-3 | FGFR3 | FGFR3_HUMAN | Fibroblast growth factor receptor | Fibroblast growth factor receptor 3 (FGFR3) | JTK4 | ||
Type: | Protein | ||
Mol. Mass.: | 87699.57 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P22607 | ||
Residue: | 806 | ||
Sequence: |
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BDBM102501 | |||
n/a | |||
Name | BDBM102501 | ||
Synonyms: | US8536175, 2 | ||
Type | Small organic molecule | ||
Emp. Form. | C29H29Cl2N5O3 | ||
Mol. Mass. | 566.478 | ||
SMILES | CCN1CCN(CC1)c1cccc(NC(=O)c2ccc(-c3c(Cl)c(OC)cc(OC)c3Cl)c3nccnc23)c1 |(-10.01,4.67,;-8.47,4.67,;-7.7,3.33,;-6.16,3.33,;-5.39,2,;-6.16,.67,;-7.7,.67,;-8.47,2,;-5.39,-.67,;-6.16,-2,;-5.39,-3.33,;-3.85,-3.33,;-3.08,-2,;-1.54,-2,;-.77,-.67,;-1.54,.67,;.77,-.67,;1.54,.67,;3.08,.67,;3.85,-.67,;5.39,-.67,;6.16,-2,;5.39,-3.33,;7.7,-2,;8.47,-3.33,;10.01,-3.33,;8.47,-.67,;7.7,.67,;8.47,2,;7.7,3.33,;6.16,.67,;5.39,2,;3.08,-2,;3.85,-3.33,;3.08,-4.67,;1.54,-4.67,;.77,-3.33,;1.54,-2,;-3.85,-.67,)| | ||
Structure |