sodium:4-[(1R,2R,3aS,8bS)-2-hydroxy-1-[(E,3S)-3-hydroxy-4-methyloct-1-en-6-ynyl]-2,3,3a,8b-tetrahydro-1H-cyclopenta[b][1]benzofuran-5-yl]butanoate
中文名称 | sodium:4-[(1R,2R,3aS,8bS)-2-hydroxy-1-[(E,3S)-3-hydroxy-4-methyloct-1-en-6-ynyl]-2,3,3a,8b-tetrahydro-1H-cyclopenta[b][1]benzofuran-5-yl]butanoate |
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中文同义词 | 贝拉前列素钠盐(非对映异构体混合物);(RAC)-贝拉前列素钠;贝前列素钠盐(非对映异构体的混合物);贝前列素杂质27;贝前列素杂质10 钠盐;贝前列素钠(非对映体混合物) |
英文名称 | sodium:4-[(1R,2R,3aS,8bS)-2-hydroxy-1-[(E,3S)-3-hydroxy-4-methyloct-1-en-6-ynyl]-2,3,3a,8b-tetrahydro-1H-cyclopenta[b][1]benzofuran-5-yl]butanoate |
英文同义词 | sodium:4-[(1R,2R,3aS,8bS)-2-hydroxy-1-[(E,3S)-3-hydroxy-4-methyloct-1-en-6-ynyl]-2,3,3a,8b-tetrahydro-1H-cyclopenta[b][1]benzofuran-5-yl]butanoate;Beraprost sodium (Relative stereochemistry);Beraprost Impurity 10 Sodium Salt;Beraprost impurity 27;Beraprost Sodium (Mixture of Diastereomers) |
CAS号 | 496807-11-5 |
分子式 | C24H31NaO5 |
分子量 | 422.5 |
EINECS号 | |
相关类别 | 贝前列素杂质 |
Mol文件 | 496807-11-5.mol |
结构式 |
sodium:4-[(1R,2R,3aS,8bS)-2-hydroxy-1-[(E,3S)-3-hydroxy-4-methyloct-1-en-6-ynyl]-2,3,3a,8b-tetrahydro-1H-cyclopenta[b][1]benzofuran-5-yl]butanoate 性质
储存条件 | Store at -20°C |
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溶解度 | 二甲基亚砜:250 mg/mL(594.57 mM) |
形态 | 固体 |
颜色 | 白色至浅黄色 |
sodium:4-[(1R,2R,3aS,8bS)-2-hydroxy-1-[(E,3S)-3-hydroxy-4-methyloct-1-en-6-ynyl]-2,3,3a,8b-tetrahydro-1H-cyclopenta[b][1]benzofuran-5-yl]butanoate 用途与合成方法
prodrug of PGI2; Vasodilator
Beraprost sodium (0.1, 1.0, and 10.0 μM; 24 hours) treatment leads to a significant increase in the number of tube formation, BPS plays an important role on angiogenic activity. Beraprost sodium (0.1, 1.0, and 10.0 μM; 24 hours) treatment let VE-cadherin at regions of cell–cell contact becomes more abundant and the morphology of endothelial cells tends to be normal compared with those cultured under hypoxia conditions.
Beraprost sodium (oral adminstration; 0.6 mg/kg; once daily; 3 or 7 days) can mitigate the development of renal interstitial fibrosis, decrease renal oxidative stress through its potential vasodilation effect, and further prevent renal interstitial fibrosis.
Animal Model: | 6-8-week-old C57Bl/6J Male Mice |
Dosage: | 0.6 mg/kg |
Administration: | Oral adminstration; 0.6 mg/kg; once daily; 3 or 7 days |
Result: | Mitigated the development of renal interstitial fibrosis. |