生物活性 | |||
---|---|---|---|
描述 | Furthermore, treatment with 0.5 μM of either KAI407 or BQR695 leads to the redistribution of GFP-PHOsh2 to the plasma membrane of parasites, aligning with the depletion of intracellular PI4P upon inhibition of PfPI4K function. BQR695, in particular, demonstrates no toxicity against mature red blood cells (RBCs), induces a schizont-stage arrest similar to that observed with imidazopyrazine-treated parasites, and exhibits cross-resistance with imidazopyrazine-resistant lines[2]. |
实验方案 | |||
---|---|---|---|
1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.84mL 0.57mL 0.28mL |
14.19mL 2.84mL 1.42mL |
28.38mL 5.68mL 2.84mL |
参考文献 |
---|