Reaction Details | |||
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Target | Focal adhesion kinase 1 | ||
Ligand | BDBM40960 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | Dose-response biochemical assay for inhibitors of Focal Adhesion Kinase (FAK) | ||
IC50 | 2179±n/a nM | ||
Citation | PubChem, PC Dose-response biochemical assay for inhibitors of Focal Adhesion Kinase (FAK) PubChem Bioassay(2007)[AID] | ||
More Info.: | Get all data from this article, Solution Info, Assay Method | ||
Focal adhesion kinase 1 | |||
Name: | Focal adhesion kinase 1 | ||
Synonyms: | FADK 1 | FAK | FAK1 | FAK1_HUMAN | FLT4 | FRNK | Focal adhesion kinase (FAK) | Focal adhesion kinase (PTK2) | Focal adhesion kinase 1 (FAK) | Focal adhesion kinase 1/vascular endothelial growth factor receptor 3 | Focal adhesion kinase-related nonkinase | PPP1R71 | PTK2 | Protein phosphatase 1 regulatory subunit 71 | Protein-tyrosine kinase 2 | VHL/Focal adhesion kinase 1 | p125FAK | pp125FAK | ||
Type: | Tyrosine-protein kinase | ||
Mol. Mass.: | 119233.17 | ||
Organism: | Homo sapiens (Human) | ||
Description: | Q05397 | ||
Residue: | 1052 | ||
Sequence: |
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BDBM40960 | |||
n/a | |||
Name | BDBM40960 | ||
Synonyms: | 2-[[[4-(4-chlorophenyl)-5-methyl-1H-pyrazol-3-yl]amino]methylene]-5,5-dimethyl-cyclohexane-1,3-quinone | 2-[[[4-(4-chlorophenyl)-5-methyl-1H-pyrazol-3-yl]amino]methylidene]-5,5-dimethyl-cyclohexane-1,3-dione | 2-[[[4-(4-chlorophenyl)-5-methyl-1H-pyrazol-3-yl]amino]methylidene]-5,5-dimethylcyclohexane-1,3-dione | MLS000084483 | SMR000048656 | cid_667314 | ||
Type | Small organic molecule | ||
Emp. Form. | C19H20ClN3O2 | ||
Mol. Mass. | 357.834 | ||
SMILES | Cc1n[nH]c(NC=C2C(=O)CC(C)(C)CC2=O)c1-c1ccc(Cl)cc1 |(8.76,5.94,;7.85,4.69,;6.31,4.69,;5.84,3.23,;7.08,2.32,;7.08,.78,;5.75,.01,;5.75,-1.53,;7.08,-2.3,;8.41,-1.53,;7.08,-3.84,;5.75,-4.61,;4.98,-5.94,;6.52,-5.94,;4.41,-3.84,;4.41,-2.3,;3.08,-1.53,;8.33,3.23,;9.79,2.75,;10.11,1.25,;11.58,.77,;12.72,1.8,;14.19,1.33,;12.4,3.31,;10.94,3.78,)| | ||
Structure |