價格 | ¥186 | ¥413 | ¥662 |
包裝 | 1mg | 5mg | 10mg |
最小起訂量 | 1mg |
發(fā)貨地 | 上海 |
更新日期 | 2024-12-12 |
中文名稱:靛玉紅-3' -單肟 | 英文名稱:Indirubin-3'-monoxime |
CAS:160807-49-8 | 品牌: TargetMol |
產(chǎn)地: 美國 | 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: 99.65% | 產(chǎn)品類別: 抑制劑 |
貨號: T5200 |
名稱 | Indirubin-3'-monoxime |
描述 | Indirubin-3'-monoxime (Indirubin-3'-oxime) is a potent inhibitor of GSK3β (IC50: 22 nM) and also inhibits CDKs ( (IC50s: 100/180/250 nM for Cdk5/p35, Cdk1/cyclin B, Cdk2/cyclin E). |
細胞實驗 | To determine the effects of aminopurvalanol and indirubin-3′-monoxime on tau phosphorylation, Sf9 cells infected with baculovirus expressing htau23 protein were treated 36 h post-infection (when cells have already expressed levels of tau sufficient for the outgrowth of cell processes) with 20 μM inhibitors for 3 h before being harvested [1]. |
激酶實驗 | Kinase activities were assayed in Buffer A or C (unless otherwise stated), at 30?°C, at a final ATP concentration of 15 μM. Blank values were subtracted, and activities were calculated as picomoles of phosphate incorporated for a 10-min incubation. The activities are usually expressed in percentage of the maximal activity, i.e. in the absence of inhibitors. Controls were performed with appropriate dilutions of dimethyl sulfoxide. In a few cases, phosphorylation of the substrate was assessed by autoradiography after SDS-PAGE [1]. |
動物實驗 | Male mice (5–6 weeks old) were randomly assigned into five groups (n = 10). Group 1: received normal pellet diet (NPD); Group 2: received a HFD; Group 3–5 received HFD for 8 weeks followed by Indirubin-3'-monoxime (IMX) treatment (0.1, 0.2 and 0.4 mg/kg i.p, respectively) once daily for 1 week. IMX was dissolved in (2.5% v/v) DMSO in saline. The mice in NPD and HFD groups received an equivalent volume of vehicle (2.5% v/v DMSO in saline). The composition of HFD was similar as described by Srinivasan. Doses of IMX were selected based on the reports available in literature. Mice were kept under standard husbandry conditions (22 ± 1 C and 60% humidity) and maintained on a 12/12-h light/dark schedule with free access to food and water for 8 weeks. Body weight was recorded weekly throughout the experimental period [4]. |
體外活性 | Indirubins是強效的GSK-3 beta抑制劑(IC50:5-50 nM)。通過GSK-3β,細菌表達的重組人tau蛋白確實在體外被磷酸化,且這種磷酸化作用可被Indirubin-3'-monoxime 以劑量依賴的方式抑制,IC50值約為100 nM [1]。Indirubin-3'-monoxime可可逆性地在G2期阻滯異步HBL-100細胞。它抑制了共識CDK磷酸化位點以及在特定CDK1/cyclin B磷酸化位點上的核仁蛋白的磷酸化 [2]。在基于細胞和無細胞的實驗中,Indirubin-3'-monoxime選擇性地抑制了5-脂氧合酶(5-LO),這是LT生物合成中的關鍵酶,其IC50值處于低μM范圍內(nèi) [3]。 |
體內(nèi)活性 | 經(jīng)IMX處理的小鼠,在血漿中的葡萄糖、甘油三酯、膽固醇、胰島素水平方面顯示出顯著下降,并在學習記憶能力上表現(xiàn)出改善;同時減輕了氧化應激和AChE活性。此外,IMX還能劑量依賴性地提高高脂飲食(HFD)喂養(yǎng)小鼠大腦中的胰島素和BDNF水平[4]。 |
存儲條件 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
溶解度 | H2O : Insoluble Ethanol : 15 mg/mL DMSO : 55 mg/mL (198.36 mM) |
關鍵字 | Indirubin 3' monoxime | Lipoxygenase | GSK-3 | LOX | inhibit | Indirubin3'monoxime | Inhibitor | CDK | Glycogen synthase kinase-3 | Glycogen synthase kinase 3 | Indirubin-3'-monoxime | Cyclin dependent kinase |
相關產(chǎn)品 | Sodium Oxamate | 5-LOX inhibitor | 5-Aminosalicylic Acid | 4-Chloro-2'-bromoacetophenone | Ribociclib | Resveratrol | CASIN | Caffeic Acid | CHIR-99021 | Abemaciclib | Malotilate | NNK |
相關庫 | 抑制劑庫 | 神經(jīng)保護化合物庫 | 經(jīng)典已知活性庫 | 已知活性化合物庫 | 抗癌細胞代謝庫 | 細胞周期化合物庫 | 激酶抑制劑庫 | 抗衰老化合物庫 | 抗氧化化合物庫 | 神經(jīng)退行性疾病化合物庫 |
成立日期 | 2013-04-18 (12年) | 注冊資本 | 566.265100萬人民幣 |
員工人數(shù) | 100-500人 | 年營業(yè)額 | ¥ 1億以上 |
主營行業(yè) | 天然產(chǎn)物,生化試劑,分子生物學,分子砌塊,生物技術服務 | 經(jīng)營模式 | 貿(mào)易,工廠,試劑,定制,服務 |
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