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TargetTyrosine-protein kinase FRK
LigandBDBM255338
Substrate/Competitorn/a
Meas. Tech.ChEMBL_2071889 (CHEMBL4727423)
IC50 154±n/a nM
Citation Liu, JGuiadeen, DKrikorian, AGao, XWang, JBabu Boga, SAlhassan, ABYu, WSelyutin, OYu, YAnand, RXu, JKelly, JDuffy, JLLiu, SYang, CWu, HCai, JBennett, CMaloney, KMTyagarajan, SGao, YDFischmann, TOPresland, JMansueto, MXu, ZLeccese, EZhang-Hoover, JKnemeyer, IGarlisi, CGStivers, PBrandish, PEHicks, AKim, RKozlowski, JA Potent, non-covalent reversible BTK inhibitors with 8-amino-imidazo[1,5-a]pyrazine core featuring 3-position bicyclic ring substitutes. Bioorg Med Chem Lett30:0 (2020) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Tyrosine-protein kinase FRK
Name:Tyrosine-protein kinase FRK
Synonyms:FRK | FRK_HUMAN | FYN-related kinase | Nuclear tyrosine protein kinase RAK | PTK5 | RAK | SRC | Tyrosine Kinase FRK
Type:Tyrosine-protein kinase
Mol. Mass.:58254.41
Organism:Homo sapiens (Human)
Description:P42685
Residue:505
Sequence:
MSNICQRLWEYLEPYLPCLSTEADKSTVIENPGALCSPQSQRHGHYFVALFDYQARTAED
LSFRAGDKLQVLDTLHEGWWFARHLEKRRDGSSQQLQGYIPSNYVAEDRSLQAEPWFFGA
IGRSDAEKQLLYSENKTGSFLIRESESQKGEFSLSVLDGAVVKHYRIKRLDEGGFFLTRR
RIFSTLNEFVSHYTKTSDGLCVKLGKPCLKIQVPAPFDLSYKTVDQWEIDRNSIQLLKRL
GSGQFGEVWEGLWNNTTPVAVKTLKPGSMDPNDFLREAQIMKNLRHPKLIQLYAVCTLED
PIYIITELMRHGSLQEYLQNDTGSKIHLTQQVDMAAQVASGMAYLESRNYIHRDLAARNV
LVGEHNIYKVADFGLARVFKVDNEDIYESRHEIKLPVKWTAPEAIRSNKFSIKSDVWSFG
ILLYEIITYGKMPYSGMTGAQVIQMLAQNYRLPQPSNCPQQFYNIMLECWNAEPKERPTF
ETLRWKLEDYFETDSSYSDANNFIR
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM255338
n/a
NameBDBM255338
Synonyms:US9481682, 116 | US9481682, 88
TypeSmall organic molecule
Emp. Form.C28H26F3N7O3
Mol. Mass.565.5463
SMILESCOc1cc(ccc1-c1nc([C@@H]2CC[C@H]3CCC(=O)N3C2)n2ccnc(N)c12)C(=O)Nc1cc(ccn1)C(F)(F)F |r|
Structure
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