Reaction Details | |||
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Target | Tyrosine-protein kinase JAK2 [808-1132] | ||
Ligand | BDBM127726 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | Inhibition Assay | ||
IC50 | >1000±n/a nM | ||
Citation | Allen, S; Andrews, SW; Condroski, KR; Haas, J; Huang, L; Jiang, Y; Kercher, T; Seo, J Substituted pyrazolo[l,5-a]pyrimidine compounds as Trk kinase inhibitors US Patent US10758542 Publication Date 9/1/2020 | ||
More Info.: | Get all data from this article, Assay Method | ||
Tyrosine-protein kinase JAK2 [808-1132] | |||
Name: | Tyrosine-protein kinase JAK2 [808-1132] | ||
Synonyms: | JAK2 | JAK2_HUMAN | Janus kinase 2 (JAK2) | Tyrosine-protein kinase JAK2 | Tyrosine-protein kinase JAK2 (808-1132) | ||
Type: | n/a | ||
Mol. Mass.: | 37984.02 | ||
Organism: | Homo sapiens (Human) | ||
Description: | 808-1132 aa of O60674 | ||
Residue: | 325 | ||
Sequence: |
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BDBM127726 | |||
n/a | |||
Name | BDBM127726 | ||
Synonyms: | US10251889, Example 100 | US10758542, Example 100 | US8791123, 99 | US9782415, Example 99 | US9796724, Example 100 | ||
Type | Small organic molecule | ||
Emp. Form. | C22H25FN6O2 | ||
Mol. Mass. | 424.4713 | ||
SMILES | O[C@H]1CCC(CC1)NC(=O)c1cnn2ccc(nc12)N1CCC[C@@H]1c1cncc(F)c1 |r,wD:23.27,1.0,(7.01,-5.81,;6.24,-4.48,;7.01,-3.14,;6.24,-1.81,;4.7,-1.81,;3.93,-3.14,;4.7,-4.48,;3.93,-.47,;5.02,.61,;6.5,.22,;4.62,2.1,;5.52,3.35,;4.62,4.59,;3.15,4.12,;1.82,4.89,;.49,4.12,;.49,2.58,;1.82,1.81,;3.15,2.58,;-.85,1.81,;-.37,.34,;-1.62,-.56,;-2.86,.34,;-2.39,1.81,;-3.16,3.14,;-2.39,4.48,;-3.16,5.81,;-4.7,5.81,;-5.47,4.48,;-7.01,4.48,;-4.7,3.14,)| | ||
Structure |