Powder: -20°C for 3 years | In solvent: -80°C for 1 year
(+)-Fluprostenol (AL-5848) 是前列腺素 F2 α 的类似物,是一种前列腺素 F2α 受体 PTGFR 激动剂,可降低输卵管糖蛋白 1 (OVGP1) 的表达。
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
1 mg | ¥ 628 | 现货 | ||
5 mg | ¥ 1,570 | 现货 | ||
10 mg | ¥ 2,520 | 现货 | ||
25 mg | ¥ 4,280 | 现货 | ||
50 mg | ¥ 6,100 | 现货 | ||
100 mg | ¥ 8,390 | 现货 | ||
1 mL * 10 mM (in DMSO) | ¥ 1,580 | 现货 |
产品描述 | (+)-Fluprostenol (AL-5848), an analogue of prostaglandin F2 alpha, is a prostaglandin F2α receptor PTGFR agonist and decreases the expression of Oviductal glycoprotein 1 (OVGP1). |
体内活性 | (+)-Fluprostenol(s.c. to rats on day 18 of pregnancy) increased cervical creep, or softness, by the following day. Doses of (+)-Fluprostenol 100-fold larger were necessary to increase uterine contractions. (+)-Fluprostenol produced falls in serum progesterone concentrations, increases in 20 alpha-dihydroprogesterone concentrations, no changes in oestradiol or relaxin concentrations and a reduction in the ovarian human chorionic gonadotrophin binding capacity in vitro. (+)-Fluprostenol was less potent in inducing cervical softness when administered per vaginam, and a dose which produced softening in pregnant rats was ineffective in ovariectomized steroid-maintained pregnant or pro-oestrous rats[3]. |
别名 | Fluprostenol, (+)-, Travoprost acid, AL-5848, 曲伏前列素酸 |
分子量 | 458.47 |
分子式 | C23H29F3O6 |
CAS No. | 54276-17-4 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 325 mg/mL (708.88 mM), Sonication is recommended.
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
DMSO | 1 mM | 2.1812 mL | 10.9058 mL | 21.8117 mL | 54.5292 mL |
5 mM | 0.4362 mL | 2.1812 mL | 4.3623 mL | 10.9058 mL | |
10 mM | 0.2181 mL | 1.0906 mL | 2.1812 mL | 5.4529 mL | |
20 mM | 0.1091 mL | 0.5453 mL | 1.0906 mL | 2.7265 mL | |
50 mM | 0.0436 mL | 0.2181 mL | 0.4362 mL | 1.0906 mL | |
100 mM | 0.0218 mL | 0.1091 mL | 0.2181 mL | 0.5453 mL |
对于不同动物的给药剂量换算,您也可以参考 更多...
请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。
母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。
您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。
(+)-Fluprostenol 54276-17-4 GPCR/G Protein Immunology/Inflammation Prostaglandin Receptor AL 5848 PTGER2 Fluprostenol, (+)- Travoprost acid Oviductal glycoprotein 1 Fluprostenol, (+) Fluprostenol inhibit Fluprostenol (+)Fluprostenol AL-5848 OVGP1 曲伏前列素酸 Inhibitor AL5848 inhibitor