
簡要描述:Alarelin 79561-22-1Alarelin acetate is a synthetic GnRH agonist.
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| 品牌 | absin | CAS | 79561-22-1 |
|---|---|---|---|
| 分子式 | C56H78N16O12 | 純度 | 98% |
| 分子量 | 1167.32 | 貨號 | abs47027724 |
| 規(guī)格 | 2mg | 供貨周期 | 現(xiàn)貨 |
| 主要用途 | is a synthetic GnRH agonist | 應(yīng)用領(lǐng)域 | 化工,生物產(chǎn)業(yè),農(nóng)林牧漁,制藥/生物制藥,綜合 |
Alarelin 79561-22-1
| 產(chǎn)品描述 | |
| 描述 | Alarelin acetate is a synthetic GnRH agonist. Alarelin is found in higher amounts than that of LH-RH in rat hypophyseal stimulation of gonadotropin secretion in vivo and in vitro and in ovulation inductions. |
| 純度 | 98% |
| 儲存/保存方法 | Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution. |
| 基本信息 | |
| 可溶性/溶解性 | 10 mM in DMSO |
| 生物活性 | |
| 靶點 | GNRH Receptor |
| In vitro(體外研究) | The cell viability in the presence of alarelin was significantly lower than that in the absence of alarelin. The maximum stimulatory effect on cell viability was achieved at a concentration of 10-5 M and it acted in a dose-dependent manner |
| In vivo(體內(nèi)研究) | Alarelin could inhibit the gastric acid secretion both by direct actions on parietal cells in rats and by inhibiting vagous function. Alarelin could significantly enhance ratio of G1 phase and decrease ratio of S phase of GSMC of rats. |
| 參考文獻 | |
| 參考文獻 |
| 研究領(lǐng)域 | |
| 研究領(lǐng)域 | NeuroscienceEndocrine system Drug DiscoverySmall Molecule DrugLead Compound Discovery |
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