• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号
首页- Products - Endocrinology/Hormones - AChR - Adenosine 5'-monophosphate monohydrate

Adenosine 5'-monophosphate monohydrate

CAS No. 18422-05-4

Adenosine 5'-monophosphate monohydrate ( 5′-AMP | 5′-Adenylic acid | A-5′-P )

产品货号. M12845 CAS No. 18422-05-4

单磷酸腺苷 (AMP) 也称为 5'-腺苷酸,是一种用作 RNA 单体的核苷酸。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
200MG ¥102 有现货
500MG ¥147 有现货
1G ¥237 有现货
1 mL x 10 mM in DMSO ¥185 有现货

生物学信息

  • 产品名称
    Adenosine 5'-monophosphate monohydrate
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    单磷酸腺苷 (AMP) 也称为 5'-腺苷酸,是一种用作 RNA 单体的核苷酸。
  • 产品描述
    Adenosine monophosphate (AMP), also known as 5'-adenylic acid, is a nucleotide that is used as a monomer in RNA. It is an ester of phosphoric acid and the nucleoside adenosine. AMP consists of a phosphate group, the sugar ribose, and the nucleobase adenine. (In Vitro):Adenosine 5'-monophosphate monohydrate is an adenosine A1 receptor agonist. Adenosine 5'-monophosphate monohydrate (5′-AMP)-induced cell toxicity is negligible at concentrations of 25 to 400?μM 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 400?μM, 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. (In Vivo):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.
  • 体外实验
    Adenosine 5'-monophosphate monohydrate is an adenosine A1 receptor agonist. Adenosine 5'-monophosphate monohydrate (5′-AMP)-induced cell toxicity is negligible at concentrations of 25 to 400?μM 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 400?μM, 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.
  • 体内实验
    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.
  • 同义词
    5′-AMP | 5′-Adenylic acid | A-5′-P
  • 通路
    Endocrinology/Hormones
  • 靶点
    AChR
  • 受体
    Adenosine A1?receptor
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    18422-05-4
  • 分子量
    365.24
  • 分子式
    C10H14N5O7P·H2O
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO: 10 mM
  • SMILES
    C1=NC2=C(C(=N1)N)N=CN2[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)O)O)O.O
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Miao Z, et al. Rheumatol Int. 2013 Aug; 33(8):2085-92.
产品手册
关联产品
  • Carbaryl

    氨基甲酸酯类杀虫剂和杀寄生虫剂。它是一种有效的抗胆碱酯酶剂,属于氨基甲酸酯类可逆胆碱酯酶抑制剂。

  • Dibucaine hydrochlor...

    Dibucaine hydrochloride (Cinchocaine hydrochloride) 是一种钠通道抑制剂。 Dibucaine hydrochloride 是有效的 SChE 抑制剂。

  • 2-Chloroadenosine

    2-氯腺苷 (CADO) 是一种代谢稳定的腺苷类似物,可与腺苷 A1、A2A 和 A3 受体结合(Ki 分别为 300、80 和 1,900 nM)。