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TargetTyrosine-protein kinase JAK1 [837-1142]
LigandBDBM400485
Substrate/Competitorn/a
Meas. Tech.In Vitro JAK Kinase Assay
IC50<5±n/a nM
Citation Huang, TXue, C Piperidin-4-yl azetidine derivatives as JAK1 inhibitors US Patent US11285140 Publication Date 3/29/2022
More Info.:Get all data from this article,  Assay Method
 
Tyrosine-protein kinase JAK1 [837-1142]
Name:Tyrosine-protein kinase JAK1 [837-1142]
Synonyms:JAK1 | JAK1 (aa 837-1142) | JAK1A | JAK1B | JAK1_HUMAN | Tyrosine-protein kinase JAK1 | Tyrosine-protein kinase JAK1 (837-1142) | Tyrosine-protein kinase JAK1 (aa 837-1142)
Type:n/a
Mol. Mass.:35230.04
Organism:Homo sapiens (Human)
Description:P23458[837-1142]
Residue:306
Sequence:
FFRAIMRDINKLEEQNPDIVSEKKPATEVDPTHFEKRFLKRIRDLGEGHFGKVELCRYDP
EGDNTGEQVAVKSLKPESGGNHIADLKKEIEILRNLYHENIVKYKGICTEDGGNGIKLIM
EFLPSGSLKEYLPKNKNKINLKQQLKYAVQICKGMDYLGSRQYVHRDLAARNVLVESEHQ
VKIGDFGLTKAIETDKEYYTVKDDRDSPVFWYAPECLMQSKFYIASDVWSFGVTLHELLT
YCDSDSSPMALFLKMIGPTHGQMTVTRLVNTLKEGKRLPCPPNCPDEVYQLMRKCWEFQP
SNRTSF
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM400485
n/a
NameBDBM400485
Synonyms:3-[(3-{3-(Cyanomethyl)-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]azetidin-1-yl}-8-azabicyclo[3.2.1]oct-8-yl)methyl]-6-(dimethylamino)-2-fluorobenzonitrile | US10695337, Example 240 | US11285140, Example 240 | US9999619, Example 240
TypeSmall organic molecule
Emp. Form.C31H33FN10
Mol. Mass.564.6591
SMILESCN(C)c1ccc(CN2C3CCC2CC(C3)N2CC(CC#N)(C2)n2cc(cn2)-c2ncnc3[nH]ccc23)c(F)c1C#N |THB:16:14:8:10.11|
Structure
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