38562-01-5

基本信息
二诺前列特罗莫
地诺前列素氮三丁醇
氨丁三醇地诺前列素
地诺前列素氨丁三醇
地诺前列腺素 氨丁三醇
前列腺素 F2ΑTRIS 盐
地诺前列素氨丁三醇 EP标准品
地诺前列素氨丁三醇 USP标准品
地诺前列素氨丁三醇/前列腺素F2ΑTRIS盐
u14585
lutalyse
PGF2αTris
Ensaprost
u-14,583e
PGF2ALPHA
Zinoprost
PGF2a-THAM
THAM PGF2α
物理化学性质
ethanol: 50mg/mL
安全数据
制备方法

551-11-1

77-86-1

38562-01-5
以(Z)-7-((1R,2R,3R,5S)-3,5-二羟基-2-((S,E)-3-羟基-1-烯-1-基)环戊基)庚-5-烯酸(前列腺素F2α,式6)和三(羟甲基)氨基甲烷为原料合成地诺前列素氨丁三醇的一般步骤:将150g前列腺素F2α(式6)的油状物与5L乙腈混合,加热至完全溶解。控制反应温度在43至47℃之间,搅拌15分钟。随后进行热过滤,收集滤液,并用乙腈洗涤残渣。将乙腈的总体积调整至21L,合并所有滤液,搅拌约5分钟。在搅拌过程中,向滤液中缓慢加入由49.2g三(羟甲基)氨基甲烷和90ml水配制成的氨丁三醇溶液。将反应混合物加热至53~57℃,保持5分钟以促进结晶沉淀的形成。加入结晶后,继续搅拌反应18~24小时。反应完成后,让反应混合物自然冷却至室温,进行过滤。用乙腈洗涤结晶三次,每次100ml。将所得结晶置于五水磷酸盐干燥剂中,进行真空干燥直至恒重,通常需要5小时以上。最终得到约180g地诺前列素氨丁三醇(7),产率为89%。
参考文献:
[1] Patent: CN106810484, 2017, A. Location in patent: Paragraph 0025
报价日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
2025/05/22 | HY-12956A | 地诺前列素氨丁三醇 Dinoprost tromethamine salt | 38562-01-5 | 1 mg | 220元 |
2025/05/22 | HY-12956A | 地诺前列素氨丁三醇 Dinoprost tromethamine salt | 38562-01-5 | 5mg | 550元 |
2025/05/22 | HY-12956A | 地诺前列素氨丁三醇 Dinoprost tromethamine salt | 38562-01-5 | 10mM * 1mLin DMSO | 605元 |
常见问题列表
FP Receptor
|
Human Endogenous Metabolite
|
Dinoprost tromethamine salt (Prostaglandin F2α tromethamine salt; 1 μM; for 24 hours) induces ER stress, autophagy, and apoptosis in goat luteal cells.
Dinoprost tromethamine salt (1 μM; for 24 hours) significantly increases the expression of GRP78 and UPR sensors.
Apoptosis Analysis
Cell Line: | Goat luteal cells |
Concentration: | 1 μM |
Incubation Time: | For 24 hours |
Result: | Significantly increased the apoptotic rate (15.62±3.12%). |
Cell Autophagy Assay
Cell Line: | Goat luteal cells |
Concentration: | 1 μM |
Incubation Time: | For 24 hours |
Result: | There was extensive overlap between LC3 and LAMP1 in luteal cells and autophagolysosomes were formed in goat luteal cells. |
Western Blot Analysis
Cell Line: | Goat luteal cells |
Concentration: | 1 μM |
Incubation Time: | For 24 hours |
Result: | The expression of GRP78 and UPR sensors including cleaved ATF6, phosphorylated-EIF2S1, EIF2S1, ATF4, phosphorylated-IRE1, autophagy-related protein LC3-II, and pro-apoptosis factor cleaved Caspase3 increased significantly in the cells. |