Prexasertib dimesylate

CAS: 1234015-58-7 货号: P656593 分子式: C20H27N7O8S2 分子量: 557.60 PubChem CID: 137364590
有货
级别和纯度: 10mM in DMSO
别名
普雷沙替布二甲磺酸盐
储存条件
充氩,-80℃储存
运输条件
特低温运输
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规格
库存
价格
数量
1ml
P656593-1ml
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¥1,350.90
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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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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


Prexasertib dimesylate (LY2606368 dimesylate) is a selective, ATP-competitive second-generation checkpoint kinase 1 (CHK1) inhibitor with a K i of 0.9 nM and an IC 50 of <1 nM. Prexasertib dimesylate inhibits CHK2 (IC 50 =8 nM) and RSK1 (IC 50 =9 nM). Prexasertib dimesylate causes double-stranded DNA breakage and replication catastrophe resulting in apoptosis . Prexasertib dimesylate shows potent anti-tumor activity

In Vitro

Prexasertib dimesylate (LY2606368 dimesylate) inhibits MELK (IC 50 =38 nM), SIK (IC 50 =42 nM), BRSK2 (IC 50 =48 nM), ARK5 (IC 50 =64 nM). Prexasertib dimesylate requires CDC25A and CDK2 to cause DNA damage. Prexasertib dimesylate (33, 100 nM; for 7 hours) results in DNA damage during S-phase in HeLa cells. Prexasertib dimesylate (8-250 nM; pre-treated for 15 minutes) inhibits CHK1 autophosphorylation (S296) and CHK2 autophosphorylation (S516) in HT-29 cells. Prexasertib dimesylate (4 nM; 24 hours) results in a large shift in cell-cycle populations from G1 and G2-M to S-phase with an accompanied induction of H2AX phosphorylation in U-2 OS cells. Prexasertib dimesylate (33 nM; for 12 hours) causes chromosomal fragmentation in HeLa cells. Prexasertib dimesylate (100 nM; 0.5 to 9 hours) induces replication stress and depletes the pool of available RPA2 for binding to DNA. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Cycle AnalysisCell Line: HeLa cells Concentration: 33, 100 nM Incubation Time: For 7 hours Result: Had an IC 50 of 37 nM and resulted in the G2-M population received DNA damage during S-phase but continued to progress through the cell cycle into an early mitosis. Western Blot AnalysisCell Line: HT-29 cells Concentration: 8, 16, 31, 63, 125, 250 nM Incubation Time: Pre-treated for 15 minutes Result: Inhibited CHK1 autophosphorylation (S296) and CHK2 autophosphorylation (S516) (IC 50 of less than 31 nM) in HT-29 cells.

In Vivo

Prexasertib dimesylate (LY2606368 dimesylate; 1-10 mg/kg; SC; twice daily for 3 days, rest 4 days; for three cycles) causes growth inhibition in tumor xenografts . Prexasertib dimesylate (15 mg/kg; SC) causes CHK1 inhibition in the blood and the phosphorylation of both H2AX (S139) and RPA2 (S4/S8) . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Female CD-1 nu-/nu- mice (26-28 g) with Calu-6 cells Dosage: 1, 3.3, or 10 mg/kg Administration: SC; twice daily for 3 days, rest 4 days; for three cycles Result: Caused statistically significant tumor growth inhibition (up to 72.3%). Animal Model: Female CD-1 nu-/nu- mice (26-28 g) with Calu-6 cells Dosage: 15 mg/kg (Pharmacokinetic Analysis) Administration: SC (200 μL) Result: CHK1 was 7 ng/mL at 12 hours and 3 ng/mL by 24 hours in plasma exposures. Phosphorylation of both H2AX (S139) and RPA2 (S4/S8) was detectable at 4 hours, showing the rapid occurrence of DNA damage.

IC50& Target:Chk1 0.9 nM (Ki) Chk1 <1 nM (IC 50 ) Chk2 8 nM (IC 50 )

规格

别名
普雷沙替布二甲磺酸盐
规格或纯度
10mM in DMSO
英文名称
Prexasertib dimesylate
生化机理
Prexasertib dimesylate(LY2606368 dimesylate)是一种选择性的 ATP 竞争性第二代检查点激酶 1(CHK1)抑制剂,其 K i 为 0.9 nM,IC 50 小于 1 nM。Prexasertib dimesylate 可抑制 CHK2(IC 50 =8 nM)和 RSK1(IC 50 =9 nM)。前
储存条件
充氩,-80℃储存
运输条件
特低温运输
名称和识别符
分子类型
小分子
PubChem CID
分子量
557.60

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本产品的 CAS 号、分子式和分子量是多少?
本产品的 CAS 号为 1234015-58-7,分子式为 C20H27N7O8S2,分子量为 557.60 g/mol。
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