Reaction Details | |||
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Target | Mitogen-activated protein kinase kinase kinase kinase 1 | ||
Ligand | BDBM548830 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | HPK1-SLP76 TR-FRET ASSAY | ||
IC50 | 1.32±n/a nM | ||
Citation | A., CD; L., CJ; Anthony, D; Xavier, F; H., FP; Shuhei, K; Bing, L; Jongwon, L; Ping, L; L., MJ; G., NA; Alexander, P; A., VB; C., YE 7-PHENYL SUBSTITUTED 2-AMINOQUINAZOLINE INHIBITORS OF HPK1 WIPOWO2022098806 Publication Date 5/12/2022 | ||
More Info.: | Get all data from this article, Assay Method | ||
Mitogen-activated protein kinase kinase kinase kinase 1 | |||
Name: | Mitogen-activated protein kinase kinase kinase kinase 1 | ||
Synonyms: | HPK1 | M4K1_HUMAN | MAP4K1 | ||
Type: | PROTEIN | ||
Mol. Mass.: | 91316.07 | ||
Organism: | Homo sapiens (Human) | ||
Description: | ChEMBL_586597 | ||
Residue: | 833 | ||
Sequence: |
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BDBM548830 | |||
n/a | |||
Name | BDBM548830 | ||
Synonyms: | WO2022098806, Compound 2-91 | WO2022098806, Compound 2-92 | ||
Type | Small organic molecule | ||
Emp. Form. | C24H22ClFN6O3S | ||
Mol. Mass. | 528.986 | ||
SMILES | Cc1c2NCCOc2ncc1-c1c(F)c(N)c2cnc(Nc3ccc(CS(C)(=O)=O)cc3)nc2c1Cl |(1.67,-1.94,;3,-1.17,;4.33,-1.94,;4.34,-3.48,;5.67,-4.25,;7,-3.48,;7,-1.94,;5.67,-1.17,;5.67,.37,;4.33,1.14,;3,.37,;1.67,1.14,;1.67,2.68,;3,3.45,;.33,3.45,;.33,4.99,;-1,2.68,;-2.33,3.45,;-3.66,2.68,;-3.66,1.14,;-5,.37,;-5,-1.17,;-6.33,-1.94,;-6.33,-3.47,;-5,-4.25,;-5,-5.79,;-3.66,-6.56,;-2.33,-5.79,;-3.66,-8.1,;-3.66,-5.02,;-3.66,-3.48,;-3.66,-1.94,;-2.33,.37,;-1,1.14,;.33,.37,;.33,-1.17,)| | ||
Structure |