官方微信|手機(jī)版|本站服務(wù)|買家中心|行業(yè)動(dòng)態(tài)|幫助

產(chǎn)品|公司|采購(gòu)|招標(biāo)

LY294002 抑制劑

參考價(jià)650.00-950.00
具體成交價(jià)以合同協(xié)議為準(zhǔn)
  • 公司名稱杭州昊鑫生物科技股份有限公司
  • 品       牌MCE
  • 型       號(hào)HY-10108
  • 所  在  地杭州市
  • 廠商性質(zhì)代理商
  • 更新時(shí)間2023/5/23 15:33:10
  • 訪問(wèn)次數(shù)683
產(chǎn)品標(biāo)簽:

LY294002

規(guī)格
10 mM * 1 mL in DMSO715.00元10000 可售
5 mg650.00元10000 可售
10 mg950.00元10000 可售
在線詢價(jià) 收藏產(chǎn)品 查看電話 同類產(chǎn)品

聯(lián)系我們時(shí)請(qǐng)說(shuō)明是 制藥網(wǎng) 上看到的信息,謝謝!

杭州昊鑫生物科技股份有限公司成立于2009年初,是一家面向生命科學(xué)領(lǐng)域,從事科研機(jī)構(gòu)、高校、院所及生產(chǎn)企業(yè)所需科研試劑、耗材,儀器銷售和服務(wù)面向全國(guó)。

產(chǎn)品和服務(wù)涵蓋生命科學(xué)研究技術(shù)的諸多方面,提供覆蓋分子生物學(xué)、細(xì)胞生物學(xué)、植物學(xué)、生物化學(xué)、蛋白組學(xué)、免疫學(xué)等領(lǐng)域的實(shí)驗(yàn)產(chǎn)品以及生物技術(shù)服務(wù)等。目前一級(jí)代理品牌有:MCE(Medchemexpress)、Biochannel、AATbio、invivogen、Abnova、Atlas、Origene、Biovision、云克?。–loud-clone)、艾德萊(Aidlab)、Cayman、Jackson、Epigentek、Prospec、Sciencell、icellbioscience(賽百慷)、hkABCbio、chondrex、Mybiosource、Abbexa、Innovrsrch、HPI、Hitobiotec、Greerlabs,Ostex,4ADI,LDN等。

經(jīng)營(yíng)理念:以誠(chéng)信為本,保證產(chǎn)品質(zhì)量求生存,創(chuàng)造企業(yè)核心競(jìng)爭(zhēng)力求發(fā)展 , 堅(jiān)持用戶至上、服務(wù)至上的原則 。


胎牛血清、MCE抑制劑激動(dòng)劑、RNA提取試劑盒、ELISA試劑盒、重組蛋白
產(chǎn)地 進(jìn)口 級(jí)別 其他
LY294002 抑制劑
LY294002 是一種廣譜 PI3K 抑制劑,抑制 PI3Kα, PI3Kδ 和 PI3Kβ 的 IC50 分別為 0.5, 0.57, 0.97 μM。LY294002 也可抑制 CK2 的活性,IC50 為 98 nM。LY294002 是一種競(jìng)爭(zhēng)性 DNA-PK 抑制劑,可逆結(jié)合 DNA-PK 的激酶結(jié)構(gòu)域,IC50 為 1.4 μM
LY294002 抑制劑 產(chǎn)品信息

LY294002 抑制劑 

注:本產(chǎn)品僅用于科研,不可用于臨床

生物活性

LY294002 is a broad-spectrum inhibitor of PI3K with IC50s of 0.5, 0.57, and 0.97 μM for PI3Kα, PI3Kδ and PI3Kβ, respectively[1]. LY294002 also inhibits CK2 with an IC50 of 98 nM[2]. LY294002 is a competitive DNA-PK inhibitor that binds reversibly to the kinase domain of DNA-PK with an IC50 of 1.4?μM. LY294002 is an apoptosis activator[3].

IC50 & Target[1][2][4]












p110α

0.5 μM (IC50)

p110δ

0.57 μM (IC50)

p110β

0.97 μM (IC50)

human CK2

98 nM (IC50)

human CK2α2

3.869 μM (IC50)

DNA-PK

1.4 μM (IC50)

體外研究
(In Vitro)

LY294002 (0-75 μM; 24 hours and 48 hours) remarkably decreases human nasopharyngeal carcinoma CNE-2Z cells in a dose-dependent fashion[4].
LY294002 (0-75 μM; 24 hours and 48 hours ) induces CNE-2Z cells apoptosis rate in dose-dependent[4].
LY294002 (10-75 μM) significantly decreases p-Akt (S473) expression levels and up-regulates caspase-9 activity in CNE-2Z cells. Total Akt protein level is not difference with different concentration[4].
LY294002 (5, 10, 100 µM; for 2 hours) treatment partially suppresses Lysophosphatidic acid (LPA)-induced (20 µM; for 4 hours) nuclear translocation of YAP, accompanied by a reduction in p-AKT levels[6].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Proliferation Assay[4]

Cell Line:CNE-2Z cells
Concentration:0 μM, 10 μM, 25 μM, 50 μM, and 75 μM
Incubation Time:24 hours and 48 hours
Result:Decreased CNE-2Z cells in a dose-dependent fashion.
體內(nèi)研究
(In Vivo)

LY294002 (10, 25, 50, 75 mg/kg; i.p.; twice weekly; for 4 weeks) significantly reduces mean NPC tumor burden in a dose-dependent manner. LY294002 (10, 25 mg/kg) is less effective in decreasing tumor burden[4].
LY294002 (1.2 mg/kg per day; i.p.; for 14 days) prevents Leptin (60 ug/kg)-induced adverse effects on spermatozoa in Sprague-Dawley rats[5].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model:Athymic nude mice (6-8 weeks) with CNE-2Z xenograft[4]
Dosage:10 mg/kg, 25 mg/kg, 50 mg/kg, and 75 mg/kg
Administration:Intraperitoneal injection; twice weekly, for 4 weeks
Result:Mean Nasopharyngeal carcinoma (NPC) tumor burden was remarkably decreased in a dose-dependent manner.
分子量

307.34

性狀

Solid

Formula

C19H17NO3

CAS 號(hào)

154447-36-6

運(yùn)輸條件

Room temperature in continental US; may vary elsewhere.

儲(chǔ)存方式
Powder-20°C3 years

4°C2 years
In solvent-80°C6 months

-20°C1 month
溶解性數(shù)據(jù)
In Vitro:

DMSO : 50 mg/mL (162.69 mM; Need ultrasonic)

Ethanol : 50 mg/mL (162.69 mM; Need ultrasonic)

配制儲(chǔ)備液
濃度溶劑體積質(zhì)量1 mg5 mg10 mg
1 mM3.2537 mL16.2686 mL32.5373 mL
5 mM0.6507 mL3.2537 mL6.5075 mL
10 mM0.3254 mL1.6269 mL3.2537 mL
*

請(qǐng)根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合適的溶劑配制儲(chǔ)備液;一旦配成溶液,請(qǐng)分裝保存,避免反復(fù)凍融造成的產(chǎn)品失效
儲(chǔ)備液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C 儲(chǔ)存時(shí),請(qǐng)?jiān)?6 個(gè)月內(nèi)使用,-20°C 儲(chǔ)存時(shí),請(qǐng)?jiān)?1 個(gè)月內(nèi)使用。

In Vivo:

請(qǐng)根據(jù)您的實(shí)驗(yàn)動(dòng)物和給藥方式選擇適當(dāng)?shù)娜芙夥桨?。以下溶解方案都?qǐng)先按照 In Vitro 方式配制澄清的儲(chǔ)備液,再依次添加助溶劑:

——為保證實(shí)驗(yàn)結(jié)果的可靠性,澄清的儲(chǔ)備液可以根據(jù)儲(chǔ)存條件,適當(dāng)保存;體內(nèi)實(shí)驗(yàn)的工作液,建議您現(xiàn)用現(xiàn)配,當(dāng)天使用; 以下溶劑前顯示的百
分比是指該溶劑在您配制終溶液中的體積占比;如在配制過(guò)程中出現(xiàn)沉淀、析出現(xiàn)象,可以通過(guò)加熱和/或超聲的方式助溶

  • 1.


    請(qǐng)依序添加每種溶劑: 0.5% CMC-Na/saline water

    Solubility: 15.71 mg/mL (51.12 mM); Suspended solution; Need ultrasonic


  • 2.


    請(qǐng)依序添加每種溶劑: 5% DMSO    95% (20% SBE-β-CD in saline)

    Solubility: 2.87 mg/mL (9.34 mM); Suspended solution; Need ultrasonic


  • 3.


    請(qǐng)依序添加每種溶劑: 10% DMSO    40% PEG300    5% Tween-80    45% saline

    Solubility: ≥ 2.25 mg/mL (7.32 mM); Clear solution


  • 4.


    請(qǐng)依序添加每種溶劑: 10% DMSO    90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.25 mg/mL (7.32 mM); Clear solution


  • 5.


    請(qǐng)依序添加每種溶劑: 10% DMSO    90% corn oil

    Solubility: ≥ 2.25 mg/mL (7.32 mM); Clear solution





同類產(chǎn)品推薦
在找 LY294002 抑制劑 產(chǎn)品的人還在看

提示

×

*您想獲取產(chǎn)品的資料:

以上可多選,勾選其他,可自行輸入要求

個(gè)人信息: