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- 文献和实验
- 技术资料
- CAS号:
163042-96-4
- 规格:
1mg/1mLx10mM(inDMSO)/5mg/10mg/25mg/50mg/100mg
| 规格: | 1mg | 产品价格: | ¥268.0 |
|---|---|---|---|
| 规格: | 1mLx10mM(inDMSO) | 产品价格: | ¥690.0 |
| 规格: | 5mg | 产品价格: | ¥596.0 |
| 规格: | 10mg | 产品价格: | ¥984.0 |
| 规格: | 25mg | 产品价格: | ¥1992.0 |
| 规格: | 50mg | 产品价格: | ¥3192.0 |
| 规格: | 100mg | 产品价格: | ¥4544.0 |
Product Introduction
Bioactivity
| 名称 | Namodenoson |
| 描述 | Namodenoson (2-Cl-IB-MECA) is an adenosine A3 receptor agonist. |
| 动物实验 | Rats were randomly assigned to two treatment groups of 6 animals, which received either two subsequent intravenous infusions of 200 μg/kg 2-chloro-N^6-(3-iodobenzyl)adenosine-5′-N-methylcarboxamide (2-Cl-IB-MECA) during 15 min or two subsequent infusions of the vehicle during 15 min. 2-Cl-IB-MECA was dissolved in dimethylsulfoxide (DMSO) and diluted with a sodium chloride solution to a final 30% (v/v) DMSO solution (a total volume of 765 μl).?Fresh solutions were prepared prior to each experiment.The effect measurements were started at least 45 min prior to the first drug infusion and lasted until 4.5 h after this infusion.?Heart rate and blood pressure were recorded continuously and serial arterial blood samples were drawn for determination of plasma histamine concentrations.?2 h after the first administration the second dose of 2-Cl-IB-MECA (or vehicle) was administered[1]. |
| 体内活性 | 首次注入Namodenoson后,血压迅速下降至初始水平的约50%。这种低血压状态持续时间短。大约15分钟后,血压开始恢复,并迅速回升至稳定值,这一稳定值显著低于对照组的血压值。在第一次注入后150分钟给予Namodenoson的第二剂量,并未引起任何低血压现象。在第二次注入期间,平均动脉压的轻微增加并不特异性于Namodenoson[1]。 |
| 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 : 31 mg/mL (56.91 mM), Sonication is recommended. 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 2 mg/mL (3.67 mM), Sonication is recommended. |
| 关键字 | P1 receptor | Namodenoson | Inhibitor | inhibit | CF102 | CF 102 | AdenosineReceptor | Adenosine Receptor | A3 |
| 相关产品 | Adenosine 5'-monophosphate monohydrate | Inosine | Theophylline | Acefylline | Adenosine 5'-monophosphate disodium salt | Theobromine | Theophylline monohydrate | Adenosine monophosphate | Sulcatone | Diphylline | Xanthine | Doxofylline |
| 相关库 | Anti-Cancer Active Compound Library | Bioactive Compound Library | Bioactive Compounds Library Max | Neurotransmitter Receptor Compound Library | Preclinical Compound Library | Anti-COVID-19 Compound Library | GPCR Compound Library | Clinical Compound Library | Membrane Protein-targeted Compound Library | Drug Repurposing Compound Library | Anti-Cancer Clinical Compound Library | Anti-Cancer Drug 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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