名稱 | Torin 2 |
描述 | Torin 2(IC50=0.25 nM), a specific and effective mTOR inhibitor, is the 800-fold greater specific activity for mTOR than PI3K and improves pharmacokinetic properties. The EC50 of Torin 2 for ATM/ATR/DNA-PK inhibition is 28 nM/35 nM/118 nM, respectively. |
細(xì)胞實(shí)驗(yàn) | For viability, MZ-CRC-1 and TT cells are seeded in quadruplicate in 96-well plates (1.0×104 cells per well) in culture media with 2.5% and 4% FBS, respectively. After 24 hours, cells are treated with Torin 2. At the indicated time point, cells are incubated for 3 hours with 10 μL of CellTiter96 AQueous One solution in 100 μL of culture media and absorbance is measured at 490 nm.(Only for Reference) |
激酶實(shí)驗(yàn) | mTOR and PI3K Cellular Assays: Cellular IC50 values for mTOR are determined using p53?/? MEFs. Cells are treated with vehicle or increasing concentrations of Torin 2 for 1 h and then lyse. Phosphorylation of S6K1 Thr-389 is monitored by immunoblotting using a phospho-specific antibody. Meanwhile, cellular IC50 values for PI3Ka are determined based on phosphorylation of Akt Thr-308 in p53?/?/mLST8?/? MEFs or human PC3 cells expressing the S473D mutant of Akt1. |
體外活性 | 在Th-MYCN 小鼠體內(nèi),Torin 2(20 mg/kg)消除MYCN腫瘤,減少M(fèi)YCN蛋白質(zhì)水平,并誘導(dǎo)細(xì)胞凋亡.在小鼠肝微粒體穩(wěn)定性試驗(yàn)中,Torin 2表現(xiàn)出>95%的藥效學(xué)響應(yīng),半衰期為11.7分鐘.在雄性Swiss albino小鼠中,靜脈內(nèi)或口服Torin 2后,體內(nèi)表現(xiàn)出最好的生物利用度為51%,半衰期為0.72小時(shí),和低清除率是19.6 mL/min/kg. |
體內(nèi)活性 | 在MZ-CRC-1和TT細(xì)胞中, Torin 2(< 50 nM)引起細(xì)胞的的活性明顯減少,Torin 2(100 nM)使細(xì)胞的遷移明顯減少。Torin 2抑制mTORC1,因此通過(guò)促進(jìn)其核轉(zhuǎn)運(yùn)激活TFEB,EC50為1.666 mM。Torin 2與PI3Kγ具有相同的結(jié)合模式,V882作為鉸鏈結(jié)合點(diǎn),在內(nèi)部疏水袋Y867,D841 和D964再提供三個(gè)作用于氨基比林側(cè)鏈的氫鍵,類似于mTOR的Y2225,D2195 和D2357。 |
存儲(chǔ)條件 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
溶解度 | DMSO : 1 mg/ml, Sonication is recommended.
|
關(guān)鍵字 | DNA-dependent protein kinase | mTOR | Autophagy | Torin-2 | inhibit | Mammalian target of Rapamycin | DNA-PK | Torin2 | Inhibitor | Torin 2 | Apoptosis |
相關(guān)產(chǎn)品 | Guanidine hydrochloride | Naringin | Valproic Acid | L-Glutamic acid | Gefitinib | Hydroxychloroquine | Dextran sulfate sodium salt (MW 4500-5500) | Stavudine | Tributyrin | L-Ascorbic acid | Paeonol | Sodium 4-phenylbutyrate |
相關(guān)庫(kù) | 抑制劑庫(kù) | 經(jīng)典已知活性庫(kù) | 已知活性化合物庫(kù) | 激酶抑制劑庫(kù) | 含氟化合物庫(kù) | 抗衰老化合物庫(kù) | 高選擇性抑制劑庫(kù) | 抗肝癌化合物庫(kù) | 酪氨酸激酶分子庫(kù) | 細(xì)胞重編程化合物庫(kù) |