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Dinoprost tromethamine salt (Synonyms: 地诺前列素氨丁三醇; Prostaglandin F2α tromethamine salt; PGF2α THAM; Prostaglandin F2α THAM) 纯度: ≥98.0%
Dinoprost tromethamine salt (Prostaglandin F2α tromethamine salt) 是一种口服有效的前列腺素 F (PGF) 受体 (FP receptor) 激动剂。Dinoprost tromethamine salt 是在子宫内膜腔上皮和黄体 (CL) 中局部产生的溶酶激素。Dinoprost tromethamine salt 在分娩过程中起关键作用。

Dinoprost tromethamine salt Chemical Structure
CAS No. : 38562-01-5
规格 | 价格 | 是否有货 | 数量 |
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10 mM * 1 mL in DMSO | ¥605 | In-stock | |
1 mg | ¥220 | In-stock | |
5 mg | ¥550 | In-stock | |
10 mg | ¥780 | In-stock | |
25 mg | ¥1550 | In-stock | |
50 mg | ¥2500 | In-stock | |
100 mg | ¥3950 | In-stock | |
200 mg | 询价 | ||
500 mg | 询价 |
* Please select Quantity before adding items.
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生物活性 |
Dinoprost tromethamine salt (Prostaglandin F2α tromethamine salt) is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist. Dinoprost tromethamine salt is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost tromethamine salt plays a key role in the onset and progression of labour[1][2]. |
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IC50 & Target[1][2] |
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体外研究 (In Vitro) |
Dinoprost tromethamine salt (Prostaglandin F2α tromethamine salt; 1 μM; for 24 hours) induces ER stress, autophagy, and apoptosis in goat luteal cells[1]. Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only. Apoptosis Analysis[1]
Cell Autophagy Assay[1]
Western Blot Analysis[1]
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Clinical Trial |
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分子量 |
475.62 |
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Formula |
C24H45NO8 |
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CAS 号 |
38562-01-5 |
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性状 |
固体 |
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颜色 |
White to off-white |
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中文名称 |
地诺前列素氨丁三醇;缓血酸胺盐 |
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结构分类 |
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初始来源 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) |
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溶解性数据 |
In Vitro:
H2O 中的溶解度 : ≥ 100 mg/mL (210.25 mM) DMSO 中的溶解度 : ≥ 100 mg/mL (210.25 mM; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO) * “≥” means soluble, but saturation unknown. 配制储备液
查看完整储备液配制表
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 * 备注:如您选择水作为储备液,请稀释至工作液后,再用 0.22 μm 的滤膜过滤除菌后使用。
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
Concentration (start) × Volume (start) = Concentration (final) × Volume (final) This equation is commonly abbreviated as: C1V1 = C2V2
In Vivo:
请根据您的 实验动物和给药方式 选择适当的溶解方案。 以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:
以下溶解方案,请直接配置工作液。建议现用现配,在短期内尽快用完。 以下溶剂前显示的百分比是指该溶剂在您配制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。
动物溶解方案计算器
请输入动物实验的基本信息:
给药剂量 mg/kg 动物的平均体重 g 每只动物的给药体积 μL 动物数量 只 由于实验过程有损耗,建议您多配一只动物的量
计算结果
工作液所需浓度 : mg/mL
该产品水溶性佳,请具体参考实测 水 / PBS / Saline 中的溶解度数据。
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纯度 & 产品资料 |
纯度: ≥98.0%
Data Sheet (629 KB) SDS (0 KB)
COA (198 KB) HNMR (266 KB) 产品使用指南 (1538 KB) |
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参考文献 |
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