ANGIOTENSIN IV TFA(12676-15-2(free base))

CAS号

分子式

C42H55F3N8O10

主要靶点

RAAS

仅限科研使用

Cat No : CM11335

Print datasheet

Synonyms

ANGIOTENSIN IV TFA(12676 15 2(free base))|ANGIOTENSIN IV TFA(12676152(free base))|ANGIOTENSIN IV TFA(12676-15-2(free base))|angiotensin AT1?receptor



产品信息

CAS号
分子式 C42H55F3N8O10
主要靶点 RAAS
主要通路 内分泌与激素
分子量 888.92
纯度 ≥98%, 此纯度可做参考,具体纯度与批次有关系,可咨询客服
储存条件 Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
别名 ANGIOTENSIN IV TFA(12676 15 2(free base))|ANGIOTENSIN IV TFA(12676152(free base))|ANGIOTENSIN IV TFA(12676-15-2(free base))|angiotensin AT1?receptor

体内活性

Rats with CCH exhibited higher levels of Aβ42, p-tau and pro-inflammatory cytokines in the brain when compared with controls. Infusion of Ang IV significantly reduced the expression of pro-inflammatory cytokines in the brains of rats with CCH. Meanwhile, the reduction of pro-inflammatory cytokines levels caused by Ang IV was reversed by divalinal-Ang IV. During the treatment, the SBP in rats was not significantly altered[1]

溶解度

DMSO:25 mg/mL (28.12 mM)

动物实验

Eight weeks after bilateral CCA ligation surgery, rats were anaesthetized with 10% chloral hydrate and placed in a stereotactic frame. The scalp was reflected under sterile surgical conditions. A brain-infusion cannula coupled via vinyl tubing to an osmotic pump was implanted into the third cerebral ventricle by surgeons who were blinded to the experimental groups. Osmotic pumps were placed subcutaneously between the scapulae and used to infuse two doses of Ang IV (20 nM, 0.15 μl/h and 100 nM, 0.15 μl/h), divalinal-Ang IV (500 nM, 0.15 μl/h) or aCSF (0.15 μl/h) into the third cerebral ventricle, lasting for six weeks. Following this surgery, the wounds were carefully closed with sutures[1]

参考文献

1.Wang QG, Xue X, Yang Y,et al.Angiotensin IV suppresses inflammation in the brains of rats with chronic cerebral hypoperfusion[J].J Renin Angiotensin Aldosterone Syst. 2018 Jul-Sep;19(3):1470320318799587.
2.Park B M , Cha S A , Lee S H , et al. Angiotensin IV protects cardiac reperfusion injury by inhibiting apoptosis and inflammation via AT4R in rats[J]. Peptides, 2016, 79:66-74.

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