...
机译:吡啶嗪酮和吡唑的发现[1,5-A]吡啶抑制剂的C-末端SRC激酶
Bristol Myers Squibb Co Res &
Dev Route 206 &
Prov Line Rd Princeton NJ 08543 USA;
Bristol Myers Squibb Co Res &
Dev Route 206 &
Prov Line Rd Princeton NJ 08543 USA;
Bristol Myers Squibb Co Res &
Dev Route 206 &
Prov Line Rd Princeton NJ 08543 USA;
Bristol Myers Squibb Co Res &
Dev Route 206 &
Prov Line Rd Princeton NJ 08543 USA;
Bristol Myers Squibb Co Res &
Dev Route 206 &
Prov Line Rd Princeton NJ 08543 USA;
Bristol Myers Squibb Co Res &
Dev Route 206 &
Prov Line Rd Princeton NJ 08543 USA;
Bristol Myers Squibb Co Res &
Dev Route 206 &
Prov Line Rd Princeton NJ 08543 USA;
Bristol Myers Squibb Co Res &
Dev Route 206 &
Prov Line Rd Princeton NJ 08543 USA;
Bristol Myers Squibb Co Res &
Dev Route 206 &
Prov Line Rd Princeton NJ 08543 USA;
Bristol Myers Squibb Co Res &
Dev Route 206 &
Prov Line Rd Princeton NJ 08543 USA;
Bristol Myers Squibb Co Res &
Dev Route 206 &
Prov Line Rd Princeton NJ 08543 USA;
Bristol Myers Squibb Co Res &
Dev Route 206 &
Prov Line Rd Princeton NJ 08543 USA;
Bristol Myers Squibb Co Res &
Dev Route 206 &
Prov Line Rd Princeton NJ 08543 USA;
Bristol Myers Squibb Co Res &
Dev Route 206 &
Prov Line Rd Princeton NJ 08543 USA;
CSK inhibitor; kinase inhibitor; immuno-oncology; Metabolite ID;
机译:吡啶嗪酮和吡唑的发现[1,5-A]吡啶抑制剂的C-末端SRC激酶
机译:新型吡唑并(1,5-a)嘧啶类作为c-Src激酶抑制剂,可减少IKr通道阻滞。
机译:具有改善的水溶性作为P110α选择性PI3激酶抑制剂的新型吡唑[1,5-A]吡啶
机译:Pyrrolo 2,3-D嘧啶和吡唑3,4-D嘧啶衍生物作为EGF受体酪氨酸激酶的选择性抑制剂
机译:磷酸酪氨酸依赖性蛋白相互作用筛选揭示了酪氨酸14上小窝蛋白1磷酸化的作用:招募C端Src激酶。
机译:C端Src激酶同源激酶(CHK)是一种独特的抑制剂可以使Src家族酪氨酸激酶的多个活性构象失活。
机译:C-末端SRC激酶 - 同源激酶(CHK),独特的抑制剂灭活SRC家族酪氨酸激酶的多重活性构象。
机译:四唑(1,5-a)吡啶和呋咱(4,5-B)吡啶-1-氧化物作为含能材料