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- 详细信息
- 文献和实验
- 技术资料
- CAS号:
305350-87-2
- 规格:
1mLx10mM(inDMSO)/1mg/2mg/5mg/10mg/25mg/50mg/100mg/500mg
| 规格: | 1mLx10mM(inDMSO) | 产品价格: | ¥306.0 |
|---|---|---|---|
| 规格: | 1mg | 产品价格: | ¥138.0 |
| 规格: | 2mg | 产品价格: | ¥174.0 |
| 规格: | 5mg | 产品价格: | ¥273.0 |
| 规格: | 10mg | 产品价格: | ¥330.0 |
| 规格: | 25mg | 产品价格: | ¥529.0 |
| 规格: | 50mg | 产品价格: | ¥794.0 |
| 规格: | 100mg | 产品价格: | ¥1320.0 |
| 规格: | 500mg | 产品价格: | ¥3176.0 |
Product Introduction
Bioactivity
| 名称 | SL327 |
| 描述 | SL327 is a selective inhibitor for MEK1/2 with IC50 of 0.18 μM/0.22 μM; able to transport through the blood-brain barrier. |
| 激酶实验 | The ligand binding competition assays are performed. Cytosolic cell extracts from Hepa-1 cells are generated by the resuspension of the cell pellets in HEDG buffer [25 mM Hepes, 1 mM EDTA, 1 mM dithiothreitol, and 10% (v/v) glycerol, pH 7.5] containing 0.4 mM leupeptin, 4 mg/mL aprotinin, and 0.3 mM phenylmethylsulfonyl fluoride, homogenization, and centrifugation at 100,000 g for 45 min. Aliquots of the supernatant (120 μg) are incubated at room temperature for 2 h with the indicated concentrations of Pifithrin-α in the presence of 3 nM [3H]TCDD in HEDG buffer. After incubation on ice with hydroxyapatite for 30 min, HEDG buffer with 0.5% Tween 80 is added. The samples are centrifuged, washed twice, resuspended in 0.2 mL of scintillation fluid, and subjected to scintillation counting. Nonspecific binding is determined using a 150-fold molar excess of TCDF and subtracted from the total binding to obtain the specific binding. The specific binding is reported relative to [3H]TCDD alone[2]. |
| 体外活性 | 30 mg/Kg SL327明显损害小鼠空间学习记忆.50 mg/kg SL327可以透过血-脑屏障,通过抑制MAPK/ERK磷酸化而抑制条件性恐惧. |
| 体内活性 | SL327对多种其他包括PKA,PKC或CamKII的激酶没有抑制效果。 |
| 存储条件 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| 溶解度 | DMSO : 50 mg/mL (149.1 mM), Sonication is recommended. Ethanol : 16.8 mg/mL (50.1 mM), Sonication is recommended. 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 2 mg/mL (5.96 mM), Sonication is recommended. |
| 关键字 | SL327 | RNASynthesis | RNA Synthesis | Mitogen-activated protein kinase kinase | MEK2 | MEK1 | MEK | MAPKK | MAP2K | Inhibitor | inhibit | DNASynthesis | DNA Synthesis | AP-1 |
| 相关产品 | Carbazole | Hexane-1,6-diol | Guanidine hydrochloride | Vidarabine | 1,4-Naphthoquinone | 5-Fluorouracil | Usnic Acid | Adenine hemisulfate | Erythromycin thiocyanate | Adenine | Docosanoic acid | Thymidine |
| 相关库 | Inhibitor Library | CNS-Penetrant Compound Library | Bioactive Compound Library | Bioactive Compounds Library Max | Anti-Colorectal Cancer Compound Library | Kinase Inhibitor Library | Anti-Aging Compound Library | Highly Selective Inhibitor Library | Immunology/Inflammation Compound Library | Pain-Related Compound Library | Reprogramming Compound Library | Anti-Prostate Cancer Compound Library |
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文献和实验网络 第十九章 杂环化合物和生物碱 杂环化合物在自然界分布很广,其数量几乎占已知有机化合物的三分之一,用途也很多。许多重要的物质如叶绿素、血红素、核酸以及临床应用的一些有显著疗效的天然药物和合成药物等,都含有杂环化合物的结构。生物碱多是中草药的有效成分,绝大多数是含氮的杂环化合物。本章内容与医学关系密切,具有重要意义。
分子中具有高能键的化合物。在生物体内主要有上式(Ⅰ)和(Ⅱ)两种结构的高能化合物。其作用为贮藏能量(例如 ATP、肌酸磷酸)和作为产生 ATP源的中间代谢产物(例如磷酸烯醇丙酮酸)以及合成反应的中间物质(例如酰基辅酶 A),在蛋白质的结构( conformation)变化周期的第一阶段上(例如钠钾 ATP酶的羧基磷酸中间体)也具有重要作用。多数高等化合物具有磷酸基,但也有例外。
由不同种元素组成的纯净物叫做化合物。化合物一般有固定的组成。化合物的组成一般可用化学式表示。化合物具有确定的物理性质和化学性质,不同于其组成元素的性质。化合物中的元素不能用简单的机械方法或物理方法分开,而必须用化学方法才能分离。
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