轻松扫码查看产品文档 | TCIMAIL No.197 已上新 | TCI试剂——品质可靠,值得信赖
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CAS RN: 144689-24-7 | 产品编码: O0507
Olmesartan
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* 无具体发货日期的情况,如:显示“8个工作日后发货”,将在您订购日起的8个工作日后发货。
* 我们将以最优方式从上海/天津两大仓库发货。国内库存不足,需两周左右向日本总部调货。
* 对于可分装产品,11:30前的订单,当天发货;11:30后的订单,隔天发货。
* 如需大包装,请点击“大包装询价”按钮(对于某些产品我们无法提供大包装)。
* TCI会经常复审储藏条件以对其进行优化,请以在线目录为准,敬请留意。
* 更多信息,请联系营业部:021-67121386 / Sales-CN@TCIchemicals.com 。任何货期、规格或包装方面的需求,请联系我们 。
产品编码 | O0507 |
纯度/分析方法 | >98.0%(HPLC) |
分子式/分子量 | C__2__4H__2__6N__6O__3 = 446.51 |
外观与形状(20°C) | 固体 |
储存温度 | 冷冻 (<0°C) |
应避免的情况 | 加热 |
包装和容器 | 100MG-带有塑料内管的玻璃瓶 (查看图片) |
CAS RN | 144689-24-7 |
Reaxys-RN | 7502669 |
PubChem物质ID | 354335584 |
MDL编号 | MFCD00914967 |
技术规格
Appearance | White to Light yellow powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Purity(Neutralization titration) | min. 95.0 % |
物性(参考值)
熔点 | 177 °C(dec.) |
GHS
相关法规
RTECS# | NI4014100 |
新化学物质备案回执号 | B1A232215179 |
运输信息
监管条件代码(*) |
应用
Olmesartan: A Selective AT1 Subtype Angiotensin II Receptor Antagonist (“sartan”)
Olmesartan, an active metabolite of olmesartan medoxomil [O0510], is a selective AT1 subtype angiotensin II receptor antagonist (“sartan”), such as candesartan [C2635], eprosartan [E1161], irbesartan [I0859], losartan [L0232], olmesartan [O0507], telmisartan [T2861] and valsartan [V0112].
Angiotensin II is formed from angiotensin I in a reaction catalyzed by angio-tensin converting angiotensin conversion enzyme (ACE), and can active two different receptors, AT1 and AT2, both of which are coupled to G-protein. The vasopressor actions of angiotensin II are mediated through AT1 receptors. Olmesartan and sartans bind selectively to AT1 receptor with almost no binding to AT2 receptor in vascular smooth muscle. Therefore, olmesartan and sartans show blood pressure lowering effect. Recently, some combination agents with a calcium channel antagonist (e.g. amlodipine [A2353], azelnidipine [A2433]) are also used for the treatment of hypertension and cardiovascular disease. (The product is for research purpose only.)
Angiotensin II is formed from angiotensin I in a reaction catalyzed by angio-tensin converting angiotensin conversion enzyme (ACE), and can active two different receptors, AT1 and AT2, both of which are coupled to G-protein. The vasopressor actions of angiotensin II are mediated through AT1 receptors. Olmesartan and sartans bind selectively to AT1 receptor with almost no binding to AT2 receptor in vascular smooth muscle. Therefore, olmesartan and sartans show blood pressure lowering effect. Recently, some combination agents with a calcium channel antagonist (e.g. amlodipine [A2353], azelnidipine [A2433]) are also used for the treatment of hypertension and cardiovascular disease. (The product is for research purpose only.)
References
- In vitro and in vivo pharmacology of olmesartan medoxomil, an angiotensin II type AT1 receptor antagonist (a review)
- Angiotensin II Receptor Antagonists and Angiotensin-Converting Enzyme Inhibitors Lower In Vitro the Formation of Advanced Glycation End Products: Biochemical Mechanisms
- Olmesartan medoxomil, a novel potent angiotensin II blocker (a review)
- H. Koike, T. Konse, T. Sada, T. Ikeda, A. Hyogo, D. Hinman, H. Saito, H. Yanagisawa, Annu. Rep. Sankyo Res. Lab. 2004, 55, 1.
- Calcium channel blocker azelnidipine enhances vascular protective effects of AT1 receptor blocker olmesartan
- Olmesartan/amlodipine: a review of its use in the management of hypertension
- Quantitative determination of olmesartan in human plasma and urine by liquid chromatography coupled to tandem mass spectrometry
- Identification of a degradation product in stressed tablets of olmesartan medoxomil by the complementary use of HPLC hyphenated techniques
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