價(jià)格 | ¥263 | ¥369 | ¥663 |
包裝 | 1mg | 2mg | 5mg |
最小起訂量 | 1mg |
發(fā)貨地 | 上海 |
更新日期 | 2024-12-12 |
中文名稱:化合物 LY-294002 hydrochloride | 英文名稱:LY-294002 hydrochloride |
CAS:934389-88-5 | 品牌: TargetMol |
產(chǎn)地: 美國(guó) | 保存條件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
純度規(guī)格: 99.95% | 產(chǎn)品類別: 抑制劑 |
貨號(hào): T4079 |
名稱 | LY-294002 hydrochloride |
描述 | LY-294002 hydrochloride (NSC 697286) is a synthetic molecule inhibitor of PI3Kα/δ/β (IC50: 0.5/0.57/0.97 μM, in cell-free assays); more stable than Wortmannin in solution, and also is a blocker of autophagosome formation. |
細(xì)胞實(shí)驗(yàn) | Cell lines: Colon cancer cell lines DLD-1,LoVo,HCT15,and Colo205. Concentrations: 0–50 μM. Incubation Time: 0–48 hours. Method: 1.0×105 cells (100 μL volume/well) are inoculated into 96-well microtiter plates.LY294002 is added to triplicate wells and cultured at 37oC for 0–48 hours.After treatment,Premix WST-1 (10 μL) is added to each microculture well,and the plates are incubated for 60 minutes at 37oC,after which absorbance at 450 nm is measured with a microplate reader.[2] |
激酶實(shí)驗(yàn) | PI3K inhibition by LY294002 is determined in a radiometric assay using purified, recombinant enzymes with 1 μM ATP. The kinase reaction is carried out for 1 hour at room temperature (24oC) and is terminated by addition of PBS. IC50 values are subsequently determined using a sigmoidal dose-response curve fit (variable slope). CK2 and GSK3β (glycogen synthase kinase 3β) inhibition are established by kinase selectivity screening. LY294002 is tested against the Upstate panel of kinases in 10 μM ATP.[4] |
動(dòng)物實(shí)驗(yàn) | Animal Models: Two groups of athymic nude mice (5–7 weeks) are inoculated i.p.with OVCAR-3 cells. Formulation: Dissolved in DMSO plus 0.25 ml of PBS. Dosages: 0–100 mg/kg. Administration: i.p.[3] |
體外活性 | LY294002通過(guò)失活A(yù)kt/PKB,從而抑制細(xì)胞增殖并誘導(dǎo)凋亡。在這些結(jié)腸癌細(xì)胞系中,LY294002表現(xiàn)出顯著的生長(zhǎng)抑制和誘導(dǎo)凋亡效應(yīng),并降低磷酸化Akt(Ser473)[2]的表達(dá)。LY294002使腫瘤細(xì)胞的胞質(zhì)體積減小,核固縮明顯。此外,LY294002還特異性引起細(xì)胞生長(zhǎng)G1期阻滯,幾乎完全抑制黑色素瘤細(xì)胞的增殖,并部分抑制MG-63(成骨肉瘤細(xì)胞系)的增殖[3]。 |
體內(nèi)活性 | LY294002能有效抑制腫瘤生長(zhǎng)并誘導(dǎo)凋亡,特別是在LoVo腫瘤中表現(xiàn)出顯著效果。因此,在小鼠腹膜炎癌癥模型中展現(xiàn)出了卓越的效能[2]。LY294002顯著地抑制卵巢癌的生長(zhǎng)和腹水形成[3]。 |
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 : 50 mg/mL (145.43 mM) Ethanol : 5 mM |
關(guān)鍵字 | Phosphoinositide 3-kinase | NPC | tumor | nuclear | DNA-PK | Casein Kinase | Inhibitor | PI3K | CNE-2Z | Human | inhibit | LY-294002 Hydrochloride | Lysophosphatidic acid | nasopharyngeal | DNA-dependent protein kinase | Leptin | NSC-697286 | LY294002 Hydrochloride | phosphatidylinositol 3-kinase | spermatozoa | broad-spectrum | translocation | SF1101 | LY 294002 hydrochloride | LY-294002 | SF-1101 | LY294002 | LY294002 hydrochloride | Apoptosis | NSC697286 | reversibly | carcinoma | LY 294002 Hydrochloride |
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相關(guān)庫(kù) | 抑制劑庫(kù) | 經(jīng)典已知活性庫(kù) | 抗癌活性化合物庫(kù) | 已知活性化合物庫(kù) | 激酶抑制劑庫(kù) | 抗衰老化合物庫(kù) | 抗抑郁癥化合物庫(kù) | 糖酵解化合物庫(kù) | 神經(jīng)元分化化合物庫(kù) | 細(xì)胞重編程化合物庫(kù) |
成立日期 | 2013-04-18 (12年) | 注冊(cè)資本 | 566.265100萬(wàn)人民幣 |
員工人數(shù) | 100-500人 | 年?duì)I業(yè)額 | ¥ 1億以上 |
主營(yíng)行業(yè) | 天然產(chǎn)物,生化試劑,分子生物學(xué),分子砌塊,生物技術(shù)服務(wù) | 經(jīng)營(yíng)模式 | 貿(mào)易,工廠,試劑,定制,服務(wù) |
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