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TargetTyrosine-protein kinase JAK2 [828-1132]
LigandBDBM400285
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 US9999619 Publication Date 6/19/2018
More Info.:Get all data from this article,  Assay Method
 
Tyrosine-protein kinase JAK2 [828-1132]
Name:Tyrosine-protein kinase JAK2 [828-1132]
Synonyms:JAK2 | JAK2 (aa 828-1132) | JAK2_HUMAN | Tyrosine-protein kinase JAK2
Type:n/a
Mol. Mass.:35579.28
Organism:Homo sapiens (Human)
Description:O60674[828-1132]
Residue:305
Sequence:
GALGFSGAFEDRDPTQFEERHLKFLQQLGKGNFGSVEMCRYDPLQDNTGEVVAVKKLQHS
TEEHLRDFEREIEILKSLQHDNIVKYKGVCYSAGRRNLKLIMEYLPYGSLRDYLQKHKER
IDHIKLLQYTSQICKGMEYLGTKRYIHRDLATRNILVENENRVKIGDFGLTKVLPQDKEY
YKVKEPGESPIFWYAPESLTESKFSVASDVWSFGVVLYELFTYIEKSKSPPAEFMRMIGN
DKQGQMIVFHLIELLKNNGRLPRPDGCPDEIYMIMTECWNNNVNQRPSFRDLALRVDQIR
DNMAG
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM400285
n/a
NameBDBM400285
Synonyms:US10695337, Example 39 | US11285140, Example 39 | US9999619, Example 40
TypeSmall organic molecule
Emp. Form.C27H27FN8O2
Mol. Mass.514.5541
SMILESCOc1cccc(F)c1C(=O)N1CCC(CC1)N1CC(CC#N)(C1)n1cc(cn1)-c1ncnc2[nH]ccc12
Structure
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