K-975

CAS: 2563855-03-6 货号: K655238 分子式: C16H14ClNO2 分子量: 287.74 PubChem CID: 155353714
有货
级别和纯度: 10mM in DMSO
储存条件
-80℃储存
运输条件
特低温运输
★
规格
库存
价格
数量
1ml
K655238-1ml
期货 Stock Image
¥1,650.90
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为什么选择此级别

,适用于对基线干扰要求严格的色谱和分析工作流程。

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-80℃储存。特低温运输 。请查阅批次 COA 获取详细规格。

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文献证明

在色谱分析、有机合成和交叉偶联反应领域已被 0 篇同行评审文献引用。

概述


K-975 is a potent, selective and orally active TEAD inhibitor, with a strong inhibitory effect against protein-protein interactions between YAP1/TAZ and TEAD. K-975 covalently binds to Cys359 located in the palmitate-binding pocket of TEAD via an acrylamide structure. K-975 exhibits antitumor activity on malignant pleural mesothelioma

In Vitro

K-975 (0.1-10000 nM; 144 h) inhibits the cell proliferation of NF2-non-expressing malignant pleural mesothelioma (MPM) cell lines. K-975 (10-10000 nM; 24 h) inhibits protein-protein interaction (PPI) between Halo-YAP and endogenous TEAD1/4 and Halo-TAZ and TEAD1/4 in NCI-H226 cells. K-975 (0.1-10000 nM; 24 h) strongly inhibits the reporter activity in NCI-H661/CTGF-Luc cells, with the maximum inhibition of ~70%, and does not inhibit the reporter activity in NCI-H661/NRF2-Luc cells. K-975 (1-10000 nM; 24 h) decreases the expressions of CTGF , IGFBP3 , and NPPB mRNAs, and increases the expression of FBXO32 mRNA in NCI-H226 cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Proliferation AssayCell Line: NF2-non-expressing MPM and NF2-expressing malignant MPM cells Concentration: 0.1, 1, 10, 100, 1000, 10000 nM Incubation Time: 144 hours Result: Had a stronger inhibitory effect against NF2-non-expressing cell lines than NF2-expressing cell lines. Inhibited the proliferation of MSTO-211H cells, an NF2-expressing cell line. Western Blot AnalysisCell Line: NCI-H226 cells Concentration: 10, 100, 1000, 10000 nM Incubation Time: 24 hours Result: Inhibited TEAD1-YAP1 PPI and TEAD4-YAP1 PPI. Inhibited TEAD1-TAZ PPI and TEAD4-TAZ PPI.

In Vivo

K-975 (10-300 mg/kg; p.o. twice a day for 14 days) inhibits the tumor growth by inhibiting YAP1/TAZ-TEAD signaling in MPM xenograft mouse models . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Male SCID mice (5 weeks) injected with NCI-H226 or MSTO-211H cells Dosage: 10, 30, 100, 300 mg/kg Administration: P.o. twice a day for 14 days Result: Exhibited strong anti-tumor effect in MPM s.c. xenograft mouse models.\nDecreased the expressions of CTGF , IGFBP3 , and NPPB , and increased the expression of FBXO32 in the NCI-H226 xenograft model.

IC50& Target:TEAD

规格

规格或纯度
10mM in DMSO
英文名称
K-975
生化机理
K-975 是一种强效、选择性和口服活性 TEAD 抑制剂,对 YAP1/TAZ 和 TEAD 之间的蛋白-蛋白相互作用有很强的抑制作用。K-975 通过丙烯酰胺与位于 TEAD 棕榈酸酯结合袋中的 Cys359 共价结合,从而抑制 TEAD 与 YAP1/TAZ 之间的蛋白质相互作用。
储存条件
-80℃储存
运输条件
特低温运输
作用类型
抑制剂
名称和识别符
分子类型
小分子
PubChem CID
分子量
287.74

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常见问题

本产品应如何储存?
请于?80 °C条件下保存。需超低温保存以维持规定的有效期。
本产品如何运输?
本产品采用干冰配冷袋冷冻运输。收货后请立即拆包,并按上述储存条件保存;处理干冰时请戴隔热手套并保持通风。
本产品的 CAS 号、分子式和分子量是多少?
本产品的 CAS 号为 2563855-03-6,分子式为 C16H14ClNO2,分子量为 287.74 g/mol。
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