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TargetFocal adhesion kinase 1 [410-689]
LigandBDBM25121
Substrate/Competitorn/a
Meas. Tech.In Vitro Activity Assay
IC50 121±n/a nM
Citation Luzzio, MJFreeman-Cook, KDBhattacharya, SKHayward, MMHulford, CAAutry, CLZhao, XXiao, JNelson, KL Sulfonyl amide derivatives for the treatment of abnormal cell growth US Patent US10450297 Publication Date 10/22/2019
More Info.:Get all data from this article,  Assay Method
 
Focal adhesion kinase 1 [410-689]
Name:Focal adhesion kinase 1 [410-689]
Synonyms:FAK | FAK1 | FAK1_HUMAN | Focal adhesion kinase 1 (FAK) (aa 410-689) | PTK2
Type:Enzyme Catalytic Domain
Mol. Mass.:32163.33
Organism:Homo sapiens (Human)
Description:aa 410-689
Residue:280
Sequence:
PSTRDYEIQRERIELGRCIGEGQFGDVHQGIYMSPENPALAVAIKTCKNCTSDSVREKFL
QEALTMRQFDHPHIVKLIGVITENPVWIIMELCTLGELRSFLQVRKYSLDLASLILYAYQ
LSTALAYLESKRFVHRDIAARNVLVSSNDCVKLGDFGLSRYMEDSTYYKASKGKLPIKWM
APESINFRRFTSASDVWMFGVCMWEILMHGVKPFQGVKNNDVIGRIENGERLPMPPNCPP
TLYSLMTKCWAYDPSRRPRFTELKAQLSTILEEEKAQQEE
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM25121
n/a
NameBDBM25121
Synonyms:4-{[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-5,6,7,8-tetrahydropteridin-2-yl]amino}-3-methoxy-N-(1-methylpiperidin-4-yl)benzamide | BI 2536 | CHEMBL513909 | US10450297, Example 300 | US8598172, 5
TypeSmall organic molecule
Emp. Form.C28H39N7O3
Mol. Mass.521.6544
SMILESCC[C@H]1N(C2CCCC2)c2nc(Nc3ccc(cc3OC)C(=O)NC3CCN(C)CC3)ncc2N(C)C1=O |r|
Structure
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