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TargetTyrosine-protein kinase JAK2 [826-1132]
LigandBDBM458852
Substrate/Competitorn/a
Meas. Tech.In Vitro JAK kinase Assays
IC50 0.500±n/a nM
Citation Esteve Trias, CTaltavull Moll, JGonzalez Rodriguez, JVidal Juan, B 2-(pyrazolopyridin-3-yl)pyrimidine derivatives as JAK inhibitors US Patent US10759793 Publication Date 9/1/2020
More Info.:Get all data from this article,  Assay Method
 
Tyrosine-protein kinase JAK2 [826-1132]
Name:Tyrosine-protein kinase JAK2 [826-1132]
Synonyms:JAK2 | JAK2_HUMAN | Tyrosine-protein kinase JAK2 (826-1132) | Tyrosine-protein kinase JAK2 JH1 (826-1132)
Type:Enzyme Catalytic Domain
Mol. Mass.:35849.63
Organism:Homo sapiens (Human)
Description:aa 826-1132
Residue:307
Sequence:
RIGALGFSGAFEDRDPTQFEERHLKFLQQLGKGNFGSVEMCRYDPLQDNTGEVVAVKKLQ
HSTEEHLRDFEREIEILKSLQHDNIVKYKGVCYSAGRRNLKLIMEYLPYGSLRDYLQKHK
ERIDHIKLLQYTSQICKGMEYLGTKRYIHRDLATRNILVENENRVKIGDFGLTKVLPQDK
EYYKVKEPGESPIFWYAPESLTESKFSVASDVWSFGVVLYELFTYIEKSKSPPAEFMRMI
GNDKQGQMIVFHLIELLKNNGRLPRPDGCPDEIYMIMTECWNNNVNQRPSFRDLALRVDQ
IRDNMAG
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  Blast E-value cutoff:
BDBM458852
n/a
NameBDBM458852
Synonyms:US10759793, Example 5
TypeSmall organic molecule
Emp. Form.C21H23FN6O2
Mol. Mass.410.4447
SMILESOCCOc1nc(nc(N[C@H]2CC[C@H](CC#N)CC2)c1F)-c1cnn2ccccc12 |r,wU:13.13,wD:10.9,(-6.69,6.76,;-6.21,5.3,;-4.71,4.98,;-4.23,3.51,;-2.73,3.19,;-2.25,1.73,;-.74,1.41,;.29,2.55,;-.19,4.02,;.84,5.16,;2.35,4.84,;2.82,3.38,;4.33,3.06,;5.36,4.2,;6.87,3.88,;7.9,5.02,;8.93,6.17,;4.88,5.67,;3.38,5.99,;-1.7,4.34,;-2.17,5.8,;-.27,-.06,;-1.17,-1.3,;-.27,-2.55,;1.2,-2.07,;2.53,-2.84,;3.86,-2.07,;3.86,-.53,;2.53,.24,;1.2,-.53,)|
Structure
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