Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4459 |
PK11000
|
DNA Alkylator/Crosslinker | DNA Damage/DNA Repair |
PK11000 是一种烷化剂,可通过共价半胱氨酸修饰来稳定野生型和突变型p53的 DNA 结合结构域。 | |||
T14554 |
BI-0252
|
Others | Others |
BI-0252 is an inhibitor of MDM2-p53 (IC50:4 nM). BI-0252 can induce tumor regressions in all animals of a mouse SJSA-1 xenograft. And it concomitant induction of the tumor protein p53 (TP53) target genes and markers of apoptosis. | |||
T26610 |
AM-6761
AM 6761,AM6761 |
||
AM-6761 is a potent inhibitor of the MDM2-p53 interaction. In the SJSA-1 osteosarcoma xenograft model, AM-6761 shows excellent antitumor activity with an ED50 of 11 mg/kg. | |||
T78753 | Aurora Kinases-IN-4 | Aurora Kinase | Cell Cycle/Checkpoint; Chromatin/Epigenetic |
Aurora Kinases-IN-4(Compound 11c)是共价ATP竞争型aurora kinaseA抑制剂,具有IC50为1.7 nM。该化合物对SJSA-1、MDA-MB-231、A549和HeLa细胞系的增殖抑制效果显著,其IC50分别为4.27、1.54、3.08和6.99 μM。Aurora Kinases-IN-4适用于三阴性乳腺癌(TNBC)的相关研究。 | |||
T73895 | MI-1061 TFA | ||
MI-1061 TFA 是一种有效、口服生物可用、化学稳定性高的MDM2(MDM2-p53 互作) 抑制剂,具有低纳摩尔级别的抑制活性(IC50=4.4 nM;Ki=0.16 nM)。它能在小鼠SJSA-1 异种移植瘤组织中激活p53并诱导凋亡,展现出抗肿瘤活性。 |