3-甲基腺嘌呤,3-Methyladenine
  • 3-甲基腺嘌呤,3-Methyladenine
  • 3-甲基腺嘌呤,3-Methyladenine
  • 3-甲基腺嘌呤,3-Methyladenine

3-甲基腺嘌呤|T1879主打

71篇文献
价格 449 668 2330
包装 50mg 100mg 500mg
最小起订量 50mg
发货地 上海
更新日期 2026-01-06
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产品详情

中文名称:3-甲基腺嘌呤英文名称:3-Methyladenine
CAS:5142-23-4品牌: TargetMol
产地: 美国保存条件: store at low temperature,keep away from direct sunlight,keep away from moisture,The compound is unstable in solution. Please use soon | Powder: -20°C for 3 years | Shipping with blue ice/Shipping at ambient temperature.
纯度规格: 98.00%产品类别: 抑制剂
货号: T1879
2026-01-06 3-甲基腺嘌呤 3-Methyladenine 50mg/449RMB;100mg/668RMB;500mg/2330RMB 449 TargetMol 美国 store at low temperature,keep away from direct sunlight,keep away from moisture,The compound is unstable in solution. Please use soon | Powder: -20°C for 3 years | Shipping with blue ice/Shipping at ambient temperature. 98.00% 抑制剂

Product Introduction

Bioactivity

名称3-Methyladenine
描述3-Methyladenine (3-MA) is a PI3K inhibitor that selectively inhibits class IB PI3Kγ (IC50=60 μM) and class III VPS34 (IC50=25 μM). 3-Methyladenine inhibits autophagy.
细胞实验Cells were seeded in an 8-well coverglass-bottomed chamber for 24 hours (6×10^3 cells per well). Images were acquired automatically at multiple locations on the coverglass using a Nikon TE2000E inverted microscope fitted with a 20× Nikon Plan Apo objective, a linearly-encoded stage, and a Hamamatsu Orca-ER CCD camera. A mercury-arc lamp with two neutral density filters (for a total 128-fold reduction in intensity) was used for fluorescence illumination. The microscope was controlled using NIS-Elements Advanced Research software and housed in a custom-designed 37°C chamber with a secondary internal chamber that delivered humidified 5% CO2. Fluorescence and differential interference contrast images were obtained every 10 min for a period of 48 hours. To analyze live cell imaging movies, the time-lapse records of live cell imaging experiments were exported as an image series and analyzed manually using NIS-Elements Advanced Research software. The criteria for analyses were described previously, and lagging chromosomes in prometaphase were defined as the red fluorescence-positive materials that lingered outside the roughly formed metaphase plate for more than 3 frames (30 min) [2].
动物实验All rats were fasted for 12 h with free access to water prior to operation. After anesthesia by intraperitoneal (i.p.) injection of 2% sodium pentobarbital (0.25 mL/100 g), they were laid and fixed on the table, routinely shaven, disinfected, and draped. The rat SAP model was induced by 0.1 mL/min speed uniformly retrograde infusion of a freshly prepared 3.5% sodium taurocholate solution (0.1 mL/100 g) into the biliopancreatic duct after laparotomy. Equivalent volume of normal saline solution was substituted for 3.5% sodium taurocholate solution in the sham-operation (SO) control group. The incision was closed with a continuous 3-0-silk suture, and 2 mL/100 g of saline was injected into the back subcutaneously to compensate for the fluid loss. 180 rats were randomly divided into four groups: (1) Acanthopanax treatment group (Aca group, n = 45) where the rats were injected with 0.2% Acanthopanax injection at a dose of 3.5 mg/100 g 3 h after successful modeling via the vena caudalis once, knowing that this dosage was effective as proven in our previous experiment; (2) 3-Methyladenine treatment group (3-methyladenine group, n = 45) where the rats were injected with 100 nmol/μL 3-methyladenine solution at a dose of 1.5 mg/100 g 3 h after successful modeling via the intraperitoneal route once, knowing that this dosage was effective as proven in the literature [6]; (3) SAP model group (SAP group, n = 45) where these rats received an equivalent volume of the normal saline instead of Acanthopanax injection 3 h after successful modeling via the vena caudalis once; (4) SO group (control, n = 45) where these rats received an equivalent volume of the normal saline instead of Acanthopanax injection 3 h after successful sham-operation via the vena caudalis once. The 45 animals in each of the four groups were equally randomized into 3, 12, and 24 h subgroups for postoperative observations [4].
体外活性方法:人宫颈癌细胞 HeLa 用 3-Methyladenine (2.5-10 mM) 处理 48 h,使用 Trypan blue dye exclusion assay 检测细胞生长抑制情况。 结果:3-Methyladenine 以时间和剂量依赖的方式降低 HeLa 细胞活力。[1] 方法:脂肪细胞 3T3-L1 在没有血清的情况下用 3-Methyladenine (5 mM) 处理 4 h,使用 Western Blot 方法检测靶点蛋白表达水平。 结果:3-Methyladenine 显著降低了自噬标记物 LC3-II 的细胞内水平,增加了 p62 的表达,表明 3-Methyladenine 有效抑制自噬。[2] 方法:小鼠黑色素瘤细胞 B16 用 2DG (5 mM)、rotenone (1 μM) 和 3-Methyladenine (1.2-5 mM) 处理 24 h,使用 LDH release assay 检测细胞毒性。 结果:3-Methyladenine 剂量依赖性降低 2DG/rotenone 引起的 LDH 释放上调,保护肿瘤细胞免受糖酵解和线粒体呼吸抑制。[3]
体内活性方法:为研究 3-Methyladenine 对动脉粥样硬化的影响,将 3-Methyladenine (30 mg/kg) 腹腔注射给 HFD 喂养的 ApoE−/− 小鼠,每周两次,持续八周。 结果:在高脂肪饮食喂养的小鼠中, 3-Methyladenine 治疗显著减少了动脉粥样硬化斑块的大小,并增加了病变的稳定性。3-Methyladenine 具有多种动脉粥样硬化保护作用,包括调节巨噬细胞自噬和泡沫细胞形成以及改变免疫微环境。[4] 方法:为研究自噬的调节作用,将 3-Methyladenine (15 mg/kg ) 单剂量腹腔注射给 LPS 诱导内毒素休克的 C57/BL6 小鼠。 结果: LPS 联合 3-Methyladenine 治疗的动物在内毒素血症后表现出存活率增加,血清炎症介质 TNF-α 和 IL-6 降低。[5]
存储条件store at low temperature,keep away from direct sunlight,keep away from moisture,The compound is unstable in solution. Please use soon | Powder: -20°C for 3 years | Shipping with blue ice/Shipping at ambient temperature.
溶解度DMSO : 10.9 mg/mL (73.08 mM), Sonication is recommended.
Ethanol : 4 mg/mL (26.82 mM), Sonication is recommended. The compound is unstable in solution, please use soon.
H2O : 3 mg/mL (20.11 mM), Sonication and heating are recommended. (The compound is unstable in solution, please use soon.)
关键字Vps34 | PI3Kγ | PI3K | Phosphoinositide 3-kinase | NSC-66389 | NSC66389 | Mitophagy | Mitochondrial Autophagy | Inhibitor | inhibit | EndogenousMetabolite | Endogenous Metabolite | Autophagy | 3-Methyladenine | 3Methyladenine | 3 Methyladenine
相关产品Chitosan oligosaccharide | Glycerol | Aceglutamide | Levulinic acid | Emtricitabine | L-Pyroglutamic acid | D-(+)-Trehalose dihydrate | Sucrose | Hemin | Gluconate Calcium | Thymidine | D(+)-Raffinose pentahydrate
相关库抗癌细胞代谢库
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关键字: NSC 66389|||3-甲基腺嘌呤|||3-MA|TargetMol

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