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DUBs-IN-2

  • 產(chǎn)品貨號:CS-01Y70604
  • 產(chǎn)品價格:電議
  • 產(chǎn)品產(chǎn)地:進口、國產(chǎn)
  • 包裝類型:10 mM * 1 mL in DMSO 2mg 5mg 10mg 50mg 100mg
  • 采購熱度:252
  • 庫存:100
  • CAS號:924296-19-5
  • 方法:
  • 含量:>98.00%
  • 品牌名稱:莼試
  • 分子式:C15H9N5O
  • 分子量:275.26

簡介內(nèi)容:質(zhì)量保證、價格優(yōu)惠

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標(biāo)簽:DUBs-IN-2 

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商品詳情購物流程代測服務(wù)付款方式常見問題

化學(xué)性質(zhì):                                                                                                             

規(guī)格

10 mM * 1 mL in DMSO 2mg 5mg 10mg 50mg 100mg

CAS

924296-19-5

別名

N/A

化學(xué)名

(E)-9-(ethoxyimino)-9H-indeno[1,2-b]pyrazine-2,3-dicarbonitrile

分子式

C15H9N5O

分子量

275.26

溶解度

Soluble in DMSO

儲存條件

Store at -20°C

General tips

For obtaining a higher solubility , please warm the tube at 37 and shake it in the ultrasonic bath for a while.

Shipping Condition

Evaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request

 

產(chǎn)品描述:                                                                                                            

IC50s: 7.2 M/0.93 M for USP7/USP8, respectively.

DUBs-IN-2 is a potent deubiquitinase enzyme inhibitor.

USP7 (or HAUSP) associated with the protein Mdm2 (an E3 ubiquitin ligase) recognizes the N-terminal transactivation domain of the p53 tumor suppressor and elicites its degradation by ubiquitination. USP7 also interacts with directly essential viral proteins (p53, FOXO4, PTEN) and oncogenic pathways. In addition, phenotypes connected with USP7 silencing strongly reveal that targeting USP7 by small-molecule inhibitors may be an potential direction for antiviral and anticancer therapies. USP8 (or UBPY) interacts with many substrates, such as the epidermal growth factor receptor (EGFR), an essential for the regulating cell survival, proliferation, and differentiation pathways), and is a critical regulator of receptor endocytosis and trafficking [1].

In vitro: Human USP7 and USP8 enzymes in baculovirus-infected insect cells were overexpressed in their full-length forms, then purified by the His-tag affinity chromatography procedure. using ubiquitin C-terminal 7-amido-4-methylcoumarin (Ub–AMC) evaluates inhibition of USP7 and USP8 deubiquitinating activity. Ub–AMC is hydrolyzed by deubiquitinating enzymes, thus releasing AMC. IC50 values were calculated based on dose–response curve after dilution of this compound in eight final concentrations, ranging from 100 mm to 10 nm [1].

DUBs-IN-2 as potent inhibitors of USP7 and USP8 deubiquitinating enzymes was identified functionalized cyanopyrazines by high-throughput screening of 65092 chemically diverse compounds for activity toward full-length USP7 cysteine protease in a fluorescence-based biochemical assay [1].

In vivo: So far, no study in vivo has been conducted.

Clinical trial: So far, no clinical study has been conducted.

特別提醒:                                                                                                              

1. 本產(chǎn)品僅供科研使用。請勿用于醫(yī)藥、臨床診斷或治療,食品及化妝品等用途。請勿存放于普通住宅區(qū)。

2. 為了您的安全和健康,請穿好實驗服并佩戴一次性手套和口罩操作。

原創(chuàng)作者:上海莼試生物技術(shù)有限公司

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