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KA2507 monohydrochloride

    
10mM in DMSO

KA2507 monohydrochloride

源叶(MedMol)
T29126 一键复制产品信息
2972712-63-1
C16H15ClN6O2
358.78
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
T29126-1ml
10mM in DMSO

¥1000.00

货期:3-5天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述:

KA2507 hydrochloride 是一种高效、高选择性的 HDAC6 抑制剂 IC50=2.5 nM),无明显毒性。KA2507 hydrochloride 具有抗肿瘤和免疫调节作用。

体外研究: KA2507 hydrochloride does not inhibit the in vitro proliferation of mouse or human cancer cells at concentrations that are selective for HDAC6 inhibition. The anti-proliferative effects are only observed at high concentrations of KA2507 hydrochloride, which combines with the increased acetylation of histone H3 suggests that the anti-proliferative effects of KA2507 hydrochloride are attributable to off-target inhibition of class I HDAC as well as HDAC6.
体内研究: KA2507 hydrochloride (100-200 mg/kg; p.o.; daily; for 20 days) inhibits tumor growth in the syngeneic B16-F10 mouse melanoma model.
KA2507 hydrochloride also demonstrates antitumor efficacy in CT26 and MC38 colorectal cancer models.
Analysis of tumor samples also indicates modulation of biomarkers of antitumor immunity at efficacious dosing, with KA2507 hydrochloride administration resulting in reduced STAT3 activation (as measured by phospho-STAT3, an important suppressor of the antitumor immune response), reduced PD-L1 expression, and increased expression of MHC class I.
KA2507 hydrochloride exhibits poor oral bioavailability (mice 15%) and Cmax (mice 300 ng/mL) following oral administration (mice 200 mg/kg).
参考文献: 1. Tsimberidou AM, et al. Preclinical Development and First-in-Human Study of KA2507, a Selective and Potent Inhibitor of Histone Deacetylase 6, for Patients with Refractory Solid Tumors. Clin Cancer Res. 2021;27(13):3584-3594.
保存条件: -80℃(运输条件:冰袋低温运输)
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.787 ml 13.936 ml 27.872 ml
5 mM 0.557 ml 2.787 ml 5.574 ml
10 mM 0.279 ml 1.394 ml 2.787 ml
50 mM 0.056 ml 0.279 ml 0.557 ml
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参考文献

质检证书(COA)

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摩尔浓度计算器

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