货号:A601702 同义名: RW22164 acetate;RWJ22164 acetate
Atosiban acetate是一种宫缩抑制剂,可通过抑制催产素介导的肌层细胞钙离子释放,达到快速抑制子宫收缩的效果,常用于治疗早产。
There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.
Type | HazMat fee for 500 gram (Estimated) |
Excepted Quantity | USD 0.00 |
Limited Quantity | USD 15-60 |
Inaccessible (Haz class 6.1), Domestic | USD 80+ |
Inaccessible (Haz class 6.1), International | USD 150+ |
Accessible (Haz class 3, 4, 5 or 8), Domestic | USD 100+ |
Accessible (Haz class 3, 4, 5 or 8), International | USD 200+ |
规格 | 价格 | 会员价 | 库存 | 数量 | |||
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快速发货 顺丰冷链运输,1-2 天到达
品质保证
技术支持
免费溶解
产品名称 | Vasopressin receptor 1 ↓ ↑ | Vasopressin receptor 2 ↓ ↑ | 其他靶点 | 纯度 | |||||||||||||||
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Conivaptan hydrochloride | ✔ | 98% | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | Atosiban acetate (also known as RW22164 acetate or RWJ22164 acetate), a nonapeptide, functions as a competitive antagonist to vasopressin/oxytocin receptors and is an analog of desamino-oxytocin. It is primarily used as a tocolytic agent for the investigation of spontaneous preterm labor[1]. |
体内研究 | The neuropeptides oxytocin and arginine vasopressin, which only differ by two amino acids, are both posterior pituitary hormones. Atosiban modulates the arginine vasopressin-induced physiological impacts on the cardiovascular and renal systems of the fetus and mother. In experiments involving late-gestation sheep, administering Atosiban for one hour does not result in any fetomaternal cardiovascular modifications[1]. Atosiban also inhibits the activation of neurons expressing oxytocin receptors in the parabrachial nucleus of mice[2]. |
体外研究 | Atosiban prevents the release of IP3 triggered by oxytocin from the myometrial cell membrane, thereby reducing the release and influx of calcium within myometrial cells, and diminishing oxytocin-induced release of PGE and PGF from the decidua[1]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
0.95mL 0.19mL 0.09mL |
4.74mL 0.95mL 0.47mL |
9.49mL 1.90mL 0.95mL |
CAS号 | 914453-95-5 |
分子式 | C45H71N11O14S2 |
分子量 | 1054.241 |
别名 | RW22164 acetate;RWJ22164 acetate |
运输 | 蓝冰 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Keep in dark place,Inert atmosphere,Store in freezer, under -20°C |
溶解方案 |
DMSO: 105 mg/mL(99.6 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO H2O: 50 mg/mL(47.43 mM),配合低频超声助溶 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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动物实验配方 |