Reaction Details | |||
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Target | Focal adhesion kinase 1 | ||
Ligand | BDBM31754 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | Dose-response biochemical assay for inhibitors of Focal Adhesion Kinase (FAK) | ||
IC50 | 3572±n/a nM | ||
Citation | ![]() | ||
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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BDBM31754 | |||
n/a | |||
Name | BDBM31754 | ||
Synonyms: | MLS-0010366.0001 | N-(5-phenyl-1,2,4-thiadiazol-3-yl)-2-[(5-phenyl-3-thiazolo[2,3-c][1,2,4]triazolyl)thio]acetamide | N-(5-phenyl-1,2,4-thiadiazol-3-yl)-2-[(5-phenyl-[1,3]thiazolo[2,3-c][1,2,4]triazol-3-yl)sulfanyl]acetamide | N-(5-phenyl-1,2,4-thiadiazol-3-yl)-2-[(5-phenyl-[1,3]thiazolo[2,3-c][1,2,4]triazol-3-yl)sulfanyl]ethanamide | N-(5-phenyl-1,2,4-thiadiazol-3-yl)-2-[(5-phenylthiazolo[2,3-c][1,2,4]triazol-3-yl)thio]acetamide | cid_1589738 | ||
Type | Small organic molecule | ||
Emp. Form. | C20H14N6OS3 | ||
Mol. Mass. | 450.56 | ||
SMILES | O=C(CSc1nnc2scc(-c3ccccc3)n12)Nc1nsc(n1)-c1ccccc1 | ||
Structure | ![]() |