Reaction Details |
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Target | Protein-tyrosine kinase 6 |
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Ligand | BDBM50354443 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_771345 (CHEMBL1839617) |
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IC50 | 15±n/a nM |
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Citation | Zeng, H; Belanger, DB; Curran, PJ; Shipps, GW; Miao, H; Bracken, JB; Arshad Siddiqui, M; Malkowski, M; Wang, Y Discovery of novel imidazo[1,2-a]pyrazin-8-amines as Brk/PTK6 inhibitors. Bioorg Med Chem Lett21:5870-5 (2011) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Protein-tyrosine kinase 6 |
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Name: | Protein-tyrosine kinase 6 |
Synonyms: | BRK | Breast tumor kinase | KH domain-containing, RNA-binding, signal transduction-associated protein 1 | PTK6 | PTK6_HUMAN | Protein-tyrosine kinase 6 (BRK) | Tyrosine Kinase BRK | Tyrosine-protein kinase 6 | Tyrosine-protein kinase BRK |
Type: | Tyrosine-protein kinase |
Mol. Mass.: | 51839.11 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 451 |
Sequence: | MVSRDQAHLGPKYVGLWDFKSRTDEELSFRAGDVFHVARKEEQWWWATLLDEAGGAVAQG
YVPHNYLAERETVESEPWFFGCISRSEAVRRLQAEGNATGAFLIRVSEKPSADYVLSVRD
TQAVRHYKIWRRAGGRLHLNEAVSFLSLPELVNYHRAQSLSHGLRLAAPCRKHEPEPLPH
WDDWERPREEFTLCRKLGSGYFGEVFEGLWKDRVQVAIKVISRDNLLHQQMLQSEIQAMK
KLRHKHILALYAVVSVGDPVYIITELMAKGSLLELLRDSDEKVLPVSELLDIAWQVAEGM
CYLESQNYIHRDLAARNILVGENTLCKVGDFGLARLIKEDVYLSHDHNIPYKWTAPEALS
RGHYSTKSDVWSFGILLHEMFSRGQVPYPGMSNHEAFLRVDAGYRMPCPLECPPSVHKLM
LTCWCRDPEQRPCFKALRERLSSFTSYENPT
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BDBM50354443 |
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n/a |
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Name | BDBM50354443 |
Synonyms: | CHEMBL1836800 |
Type | Small organic molecule |
Emp. Form. | C21H22N8O |
Mol. Mass. | 402.4524 |
SMILES | Cc1cn2c(cnc2c(Nc2ccc(cc2)C(=O)N2CCNCC2)n1)-c1cn[nH]c1 |
Structure |
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