957196-63-3Relevant academic research and scientific papers
Synthesis and structure-activity relationships of 1,2,3,4-tetrahydropyrido[2,3-b]pyrazines as potent and selective inhibitors of the anaplastic lymphoma kinase
Milkiewicz, Karen L.,Weinberg, Linda R.,Albom, Mark S.,Angeles, Thelma S.,Cheng, Mangeng,Ghose, Arup K.,Roemmele, Renee C.,Theroff, Jay P.,Underiner, Ted L.,Zificsak, Craig A.,Dorsey, Bruce D.
, p. 4351 - 4362 (2010)
Dysregulation of the anaplastic lymphoma kinase (ALK) is implicated in a variety of cancers. A series of tetrahydropyrido[2,3-b]pyrazines was constructed as ring-constrained analogs of a known aminopyridine kinase scaffold. Chemistry was developed to rapidly elaborate the SAR, structural elements impacting ALK inhibitory activity were exploited, and kinase selective analogs were identified that inhibit ALK with IC50 values ～10 nM (enzyme) and ～150 nM (cell).
