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3-Methyladenine (3-甲基腺嘌呤)

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  • 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-19312
  • 所  在  地杭州市
  • 廠商性質(zhì)代理商
  • 更新時(shí)間2023/5/22 11:58:18
  • 訪問(wèn)次數(shù)410
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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
CAS號(hào) 5142-23-4 產(chǎn)地 進(jìn)口
級(jí)別 其他
3-Methyladenine 純度 0. 9991
3-Methyladenine (3-MA) 是 PI3K 的抑制劑。它通過(guò)抑制class III PI3K廣泛作為自噬 (autophagy) 的抑制劑使用。
3-Methyladenine (3-甲基腺嘌呤) 產(chǎn)品信息

3-Methyladenine  (3-甲基腺嘌呤)

注:本產(chǎn)品僅用于科研,不可用于臨床

生物活性

3-Methyladenine (3-MA) is a PI3K inhibitor. 3-Methyladenine is a widely used inhibitor of autophagy via its inhibitory effect on class III PI3K

IC50 & Target[1]











PtdIns3Kγ

60 μM (IC50, Cell Assay)

Vps34

25 μM (IC50, Cell Assay)

Autophagy

Mitophagy

Human Endogenous Metabolite










體外研究
(In Vitro)

3-Methyladenine (0-10 mM; 0-48 hours) induces caspase-dependent cell death in HeLa cells in a time-and dose-dependent manner[2].
3-Methyladenine (5 mM; 24 hours) suppresses autophagy in HeLa cells under both glucose-free conditions and normal conditions[2].
3-Methyladenine (5 mM; 0-48 hours) suppresses conversion of LC3-I to LC3-II (autophagy markers) between 12hours and 48 hours, confirms the inhibitory effects on autophagy[2].
3-Methyladenine induces cell death is independent of autophagy inhibition[2].
3-Methyladenine significantly shortens the duration of nocodazole-induced-prometaphase arrest[2].
Note:
在體外細(xì)胞培養(yǎng)實(shí)驗(yàn)中,3-MA 常用的濃度為 0.5-10 mM,所以優(yōu)先推薦直接稱取本次實(shí)驗(yàn)所需粉末量,用培養(yǎng)基全都溶解,0.22 μm 過(guò)濾器過(guò)濾除菌之后使用。建議溶液現(xiàn)配現(xiàn)用,盡快用完。

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

Cell Viability Assay[2]

Cell Line:HeLa cells
Concentration:0 mM, 2.5 mM or 5 mM, 10 mM
Incubation Time:0 hour, 24 hours and 48 hours
Result:Decreased cell viability in a time-and dose-dependent manner, and was associated with caspase-3 activation.








體內(nèi)研究
(In Vivo)

3-Methyladenine (1.5?mg/100?g; intraperitoneal injection; 3-24?hours) treatment alleviates sodium taurocholate-induced severe acute pancreatitis (SAP) in rats at both 12 hours and 24?hours[3].
3-Methyladenine inhibits autophagy of pancreatic acinar cells in sodium taurocholate-tnduced SAP[3].
3-Methyladenine also shows inhibitory effects on PI3K/Akt signaling pathway and NF-κB signaling pathway in sodium taurocholate-induced SAP[3].

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

Animal Model:10–12 weeks Specific pathogen free- (SPF-) grade healthy male Sprague-Dawley (SD) rats (250–290?g)[3]
Dosage:1.5?mg/100?g (1000 μM)
Administration:Intraperitoneal injection
Result:Alleviated Sodium Taurocholate-Induced SAP.








分子量

149.15

性狀

Solid

Formula

C6H7N5

CAS 號(hào)

5142-23-4

中文名稱

3-甲基腺嘌呤

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)



關(guān)鍵詞:過(guò)濾器
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