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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
- 保质期:
Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
- 英文名:
Adenosine 5'-Monophosphate Monohydrate
- 库存:
现询
- 供应商:
北京索莱宝科技有限公司
- CAS号:
18422-05-4
- 规格:
500mg/250mg/100mg
| 规格: | 500mg | 产品价格: | ¥390.0 |
|---|---|---|---|
| 规格: | 250mg | 产品价格: | ¥300.0 |
| 规格: | 100mg | 产品价格: | ¥180.0 |
是腺苷 A1 受体 (adenosine A1 receptor) 激动剂。
| 基本信息 | |
| CAS | No.18422-05-4 |
| 中文名称 | 腺苷-5'-单磷酸一水 |
| 英文名称 | Adenosine 5'-Monophosphate Monohydrate |
| 别名 | 5-AMPmonohydrate;腺苷-5-磷酸;5’-磷酸腺苷;2-[(pyridine-2-ylmethyl)-amino]p; |
| 分子式 | C10H14N5O7P·H2O |
| 分子量 | 365.24 |
| 溶解性 | Soluble in DMSO ≥5mg/mL |
| 纯度 | HPLC≥98% |
| 外观(性状) | White to off-white Solid |
| 储存条件 | Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year |
| EC | EINECS 200-500-0 |
| MDL | MFCD00005750 |
| SMILES | O=P(O)(OC[C@@H]1[C@H]([C@H]([C@H](N2C=NC3=C2N=CN=C3N)O1)O)O)O.O |
| 靶点 | Adenosine Receptor |
| 通路 | GPCR & G Protein |
| 背景说明 | 是腺苷 A1 受体 (adenosine A1 receptor) 激动剂。 |
| 生物活性 | The physiologically relevant nucleotide AMP is a full agonist of A(1)R. Some of the physiological effects of AMP may be direct, and not indirect through ectonucleotidases that hydrolyze this nucleotide to adenosine.[1] |
| In Vitro | AMP and a non-hydrolyzable AMP analog(deoxyadenosine 5'-monophosphonate,ACP)directly activated the adenosine A(1)receptor(A(1)R). In contrast,AMP only activated the adenosine A(2B)receptor(A(2B)R)after hydrolysis to adenosine by ecto-5'-nucleotidase(NT5E,CD73)or prostatic acid phosphatase(PAP,ACPP). Adenosine and AMP were equipotent human A(1)R agonists. [1] Adenosine 5'-monophosphate monohydrate(5′-AMP)-induced cell toxicity is negligible at concentrations of 25 to 400μM in RAW264.7 cells. Adenosine 5'-monophosphate monohydrate significantly attenuates the mRNA expression of tumor necrosis factor-α(TNF-α)and interleukin(IL)-6 in RAW264.7 cells. The dose-dependence of TNF-α and IL-6 mRNA show that at concentration of 400μM,Adenosine 5'-monophosphate monohydrate exhibits the maximum inhibition. Exposure of cells to Adenosine 5'-monophosphate monohydrate significantly reduces recruitment of NF-κB p65 to TNF-α,IL-6,and IL-1β gene promoters[2]. |
| 细胞实验 | C57BL/6J mice treated with Adenosine 5'-monophosphate monohydrate(5′-AMP)markedly increases hepatic adenosine level. Survival rate in PBS-treated mice(n=15)is 60%(8 h)and 33.3%(24 h),whereas survival rate in Adenosine 5'-monophosphate monohydrate-treated mice(n=15)is 100%(8 h)and 93.3%(24 h). Serum aspartate transaminase(AST)and alanine transaminase(ALT)levels are significantly lowered in the Adenosine 5'-monophosphate monohydrate group than in the vehicle group. The area and extent of necrosis is attenuated and the infiltration of inflammatory cells is reduced in the Adenosine 5'-monophosphate monohydrate group[2]. |
| 数据来源文献 | [1]. Rittiner JE, et al. AMP is an adenosine A1 receptor agonist. J Biol Chem. 2012 Feb 17;287(8):5301-9. [2]. Zhan Y, et al. Adenosine 5'-monophosphate ameliorates D-galactosamine/lipopolysaccharide-induced liver injury through an adenosine receptor-independent mechanism in mice. Cell Death Dis. 2014 Jan 9;5:e985. |
| 单位 | 瓶 |
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文献和实验4)2・CaF2+2OH-。 此外,氟还可直接刺激细胞膜中G蛋白,激活腺苷酸环化酶或磷脂酶C,启动细胞内cAMP或磷脂酰肌醇信号系统,引起广泛生物效应。 氟过多亦可对机体产生损伤、如长期饮用高氟(>2mg/L)水。牙釉质受损出现斑纹、牙变脆易破碎等。 七、钒 钒在人体内含量极低,体内总量不足1mg。主要分布于内脏,尤其是肝、肾、甲状腺等部位,骨组织中含量也较高。人体对钒的正常需要量为100μg/d。 钒在胃肠吸收率仅5%,其吸收部位主要在上消化道。此外环境中的钒
肾毒性。DMSO是毒性比较强的东西,用的时候要避免其挥发,要准备1%-5%的氨水备用,皮肤沾上之后要用大量的水以及稀氨水洗涤。最为常见的为恶心、呕吐、皮疹及在皮肤和呼出的气体中发出大蒜、洋葱、牡蛎味。吸入:高挥发浓度可能导致头痛,晕眩和镇静。皮肤:能够灼伤皮肤并使皮肤有刺痛感,如同所见的皮疹及水泡一样。若二甲基亚砜与含水的皮肤接触会产生热反应。要避免接触含有毒性原料或物质的二甲基亚砜溶液,因其毒性不为人所知,而二甲基亚砜却可能会渗入肌肤,在一定条件下会将有毒物质代入肌肤。吸收:吸收危险性很低。2.EB
健康。当使用固体或高浓度储存液时,戴手套和护目镜,在通风橱中操作。 7.TEMED强神经毒性,防止误吸,操作时快速,存放时密封。 8.PMSF:苯甲基磺酰氟[(PMSF),C7H7FO2S或C6H5CH2SO2F]是一种高强度毒性的胆碱酯酶抑制剂。它对呼吸道黏膜、眼睛和皮肤有非常大的破坏性。可因吸入、咽下或皮肤吸收而致命。戴合适的手套和安全眼镜,始终在化学通风橱里使用。在接触到的情况下,要立即用大量的水冲洗眼睛或皮肤,已污染的工作服丢弃掉。 9. 氯仿(CHCl3)对皮肤、眼睛
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