CAS NO: | 1092788-83-4 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 |
PP121 is a multi-targeted kinase inhibitor withIC50s of 10, 60, 12, 14, 2 nM formTOR,DNK-PK,VEGFR2,Src,PDGFR, respectively. |
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IC50& Target[1] |
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体外研究 (In Vitro) |
PP121 blocks the PI3K pathway by direct inhibition of PI3K/mTOR in two glioblastoma cell lines, U87 and LN229. PP121 potently inhibits the proliferation of a diverse panel of tumor cell lines containing mutations in the PI3-K pathway components PIK3CA, PTEN, or RAS. PP121 induces a G0G1arrest in most tumor cells. PP121 directly inhibits Src in cells and reverses its biochemical and morphological effects. PP121 potently inhibits the Ret kinase domainin vitro(IC50<1 nm). pp121 potently blocks vegf stimulated activation of the pi3-k and mapk pathways. inhibits vegfr2 autophosphorylation at low nanomolar concentrations, confirming that this molecule directly targets in cells. bcr-abl induced tyrosine phosphorylation k562 cells as well baf3 express bcr-abl[1].
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体内研究 (In Vivo) |
Oral administration of PP121 remarkably inhibits Eca-109 xenograft growth. Mice body weights are not significantly affected by PP121 or the vehicle treatment. PP121 oral administration dramatically inhibits activations of Akt-mTOR and NFkB in xenograft tumors. p-Akt Ser 473 and p-IKKa/b are both inhibited by PP121 administration[2].
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分子量 |
319.36 |
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性状 |
Solid |
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Formula |
C17H17N7 |
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CAS 号 |
1092788-83-4 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 20 mg/mL(62.63 mM;Need ultrasonic)
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In Vivo:
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