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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。
T36934	PK7242 (maleate) PK7242 (maleate)
	The protein p53, often called the 'guardian of the genome,' is a transcription factor that is activated in response to cellular stress (low oxygen levels, heat shock, DNA damage, etc.) and acts to prevent further proliferation of the stressed cell by promoting cell cycle arrest or apoptosis. Its role as a tumor suppressor is evident by the observation that approximately 50% of human tumors have mutated or non-functional p53. PK7242 is an inducer of reactivation of mutant p53 in cancer cells. In ...
T73533	ADH-6
	ADH-6，一种三吡啶酰胺化合物，消除突变p53 DBD聚集成核亚结构域的自组装，并靶向解离人类癌细胞中的突变p53聚集体。通过此过程，ADH-6恢复p53的转录活性，导致细胞周期停滞与细胞凋亡(apoptosis)，展示了其研究癌症疾病的潜力。
T74443	ADH-6 TFA
	ADH-6 TFA为三吡啶酰胺类化合物，通过靶向并解离人类癌细胞中突变p53聚集体，阻止突变p53 DBD聚集成核亚结构域的自组装，从而恢复p53的转录活性。这一过程导致细胞周期停滞和细胞凋亡(apoptosis)，显示出其在研究癌症疾病中的应用潜力。
T35696	Olomoucine II
	Olomoucine II is an inhibitor of cyclin-dependent kinases (CDKs; IC50s = 7.6, 0.1, 19.8, 0.45, and 0.06 μM for Cdk1, -2, -4, -7, and -9, respectively).1It is selective for CDKs over 10 additional kinases (IC50s = >100 μM for all) but does inhibit ERK2 (IC50= 32 μM) and the ATP-binding cassette transporter B1 (ABCB1; IC50= 6.4 μM).1,2Olomoucine II inhibits proliferation of a variety of cancer cells, including those expressing wild-type p53 or mutant p53 (mean IC50s = 7.4 and 10.1 μM, respectively...
T35874	CC260
	CC260 is a selective PI5P4Kα and PI5P4Kβ inhibitor with Kis of 40 nM and 30 nM, respectively. CC260 does not inhibit or weakly inhibits other protein kinases, such as Plk1 and RSK2. CC260 can be used for cell energy metabolism, diabetes and cancer research[1]. In cultured C2C12 myotubes, CC260 (20 μM) enhances Insulin-induced Akt phosphorylation at both Thr-308 and Ser-473 but suppresses S6K phosphorylation (Thr-389) by mTORC1[1]. CC260 (2.5 μM, 5 μM, 10 μM, 20 μM) significantly increases phosph...