• 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

A 779(3TFA)

CAS No. 159432-28-7

A 779(3TFA) ( —— )

产品货号. M21034 CAS No. 159432-28-7

779(3TFA) 是血管紧张素-(1-7) 受体的有效拮抗剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥502 有现货
10MG ¥745 有现货
25MG ¥1353 有现货
50MG ¥2025 有现货
100MG ¥3038 有现货
200MG 获取报价 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    A 779(3TFA)
  • 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
    779(3TFA) 是血管紧张素-(1-7) 受体的有效拮抗剂。
  • 产品描述
    A 779(3TFA) is a potent antagonist of angiotensin-(1-7) receptor.
  • 体外实验
    A-779 inhibits the effect of Ang-(1-7), which suppresses the proliferating cell nuclear antigen (PCNA) protein expression up-regulated by Ang II, but A-779 alone has no effect to induce proliferation and migration of VSMCs. Pretreatment with Ang-(1-7) significantly retards Ang II-induced inflammatory responses of VSMCs associated with up-regulated MCP-1, VCAM-1 and IL-1β expressions, and this effect of Ang-(1-7) is blocked by A-779. But A-779 alone has no effect to induce inflammatory response of VSMCs. Pretreatment VSMCs with Ang-(1-7) for 5?min significantly inhibits Akt and ERK1/2 phosphorylation induced by Ang II, and this effect is also blocked by A-779, but alone has no effect to induce phosphorylation of Akt and ERK1/2 in VSMCs.
  • 体内实验
    Infusion of Ang(1-7) and A-779 (400ng/kg/min, s.c.) alone or combined for 6 weeks does not prevent uterus atrophy or inhibit the body weight gain of OVX rats. A-779 markedly elevates serum bone specific alkaline phosphatase (BALP), telopeptides of collagen type I (CTX), tartarate resistant acid phosphatase (TRAcP 5b), osteocalcin (OC) and urinary deoxypyridinoline (DPD). Infusion of Ang(1-7) and/or A-779 does not significantly change serum minerals concentrations in sham or OVX groups. A-779 in the OVX animals does not change AngII, Ang(1-7), AT1R, AT2R, ACE, ACE-2, Mas receptor, RANKL and OPG proteins expressions in relation to OVX group, while AngII (P0.05), AT1R (P0.05), ACE (P0.01) and RANKL (P0.01) expressions are significantly higher and Ang(1-7), AT2R, ACE-2, MasR and OPG are significantly (P0.01) lower than sham group. Blocking of the G-protein coupled receptor (Mas) by A-779 markedly abolishes Ang(1-7) favorable effects on bone health suggesting the vital role of Mas receptor in mediating Ang(1-7) osteo-protective effects. Inhibition of Ang1-7 cascade by A-779 (400ng/kg/min) significantly eradicates captopril protective effects on bone metabolism, mineralization and micro-structure. A-779 also restores OVX effects on RANKL expression and ACE-1/AngII/AT1R cascade and down-regulates OPG expression and ACE-2/Ang1-7/Mas pathway.
  • 同义词
    ——
  • 通路
    Endocrinology/Hormones
  • 靶点
    RAAS
  • 受体
    Angiotensin Receptor
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    159432-28-7
  • 分子量
    872.97
  • 分子式
    C39H60N12O11
  • 纯度
    >98% (HPLC)
  • 溶解度
    H2O:50 mg/mL (57.28 mM; Need ultrasonic)
  • SMILES
    CCC(C)C(NC(=O)C(Cc1ccc(O)cc1)NC(=O)C(NC(=O)C(CCCNC(=N)N)NC(=O)C(N)CC(=O)O)C(C)C)C(=O)NC(Cc1cnc[nH]1)C(=O)NC(C)C(=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.Yan W F Xue J J Yang H Y et al. [Effects and related mechanism of angiotensin-(1-7) on Toll-like receptor 4-mediated oxidative stress in human umbilical vein endothelial cells].[J]. Zhonghua Xin Xue Guan Bing Za Zhi 2017 45(3):223.
产品手册
关联产品
  • A 779 3TFA(159432-28...

    A 779(3TFA) 是血管紧张素 (1-7) 受体的有效拮抗剂 A-779 抑制 Ang II 上调的增殖细胞核抗原 (PCNA) 蛋白表达,但单独使用 A-779 没有诱导增殖的作用和 VSMC 的迁移。

  • Vicenin 3

    Vicenin 3 是一种来自 Desmodium styracifolium 地上部分的血管紧张素转换酶 (ACE; IC50: 46.91 μM) 抑制剂。

  • Fosinopril sodium

    Fosinopril Sodium 是血管紧张素转换酶 (ACE) 抑制剂的酯前药。