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Cabergoline
CAS No. 81409-90-7
Cabergoline ( FCE-21336 )
产品货号. M22708 CAS No. 81409-90-7
卡麦角林是一种麦角衍生的多巴胺 D2 样受体激动剂。它对 D2、D3 和 5-HT2B 受体具有高亲和力(Ki 分别为 0.7、1.5 和 1.2)。卡麦角林通过使催乳素产生的垂体腺瘤水平正常化,可以快速有效地控制激素和肿瘤。卡麦角林可作为一种有效的药物D2、D3 和 5-HT2B 受体激动剂。
纯度: >98% (HPLC)
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规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥624 | 有现货 |
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10MG | ¥988 | 有现货 |
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25MG | ¥1968 | 有现货 |
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50MG | ¥3637 | 有现货 |
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100MG | ¥5338 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Cabergoline
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述卡麦角林是一种麦角衍生的多巴胺 D2 样受体激动剂。它对 D2、D3 和 5-HT2B 受体具有高亲和力(Ki 分别为 0.7、1.5 和 1.2)。卡麦角林通过使催乳素产生的垂体腺瘤水平正常化,可以快速有效地控制激素和肿瘤。卡麦角林可作为一种有效的药物D2、D3 和 5-HT2B 受体激动剂。
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产品描述Cabergoline is an ergot derived-dopamine D2-like receptor agonist. It has high affinity for D2, D3, and 5-HT2B receptors (Ki=0.7, 1.5, and 1.2, respectively).Cabergoline permits rapid and effective hormonal and tumor control by normalizing prolactin-producing pituitary adenomas levels.Cabergoline acts as a potent agonist of D2, D3 and 5-HT2B receptors. Cabergoline(10 μM) is used to investigate its neuroprotective effects. MAP2 staining reveals that Cabergoline significantly suppresses the loss of neurons caused by H2O2 incubation. Pretreatment with Cabergoline inhibits H2O2-induced neuronal cell death in a dose-dependent manner. The detection of apoptotic nuclear condensation suggested that Cabergoline prevents apoptotic cell death following H2O2 exposure[1].Cabergoline has a longer elimination half-life (63 to 109 h) compared with other D2-like receptor agonists, both a long-lasting clinical effect following single-dose administration. And an improvement in the quality of life of patients with chronic diseases are expected[1]. The most significant reduction in rapid eye movement (REM) sleep bout number occurred during the light phase. In which Cabergoline-injected female handled mice has 67.3% less REM sleep bouts (F(1,11)=12.892, P=0.004) than Cabergoline-injected females that are restrained, although the greatest number in reduction of REM sleep bouts occurr during the dark phase (82.3% fewer REM sleep bouts; F(1,11)=3.667, P=0.082). In male mice, Cabergoline reduces baseline Prolactin (PRL) levels (98.5%; F(1,6)=13.192, P=0.011) from 5.8±1.3 to 0.08 ng/mL within 2 hours of injection. PRL levels return to values that are not different from baseline (5.0±0.60 ng/mL; F(1,6)=0.715, P=0.43), after a 7-day recovery period.
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体外实验——
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体内实验——
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同义词FCE-21336
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通路GPCR/G Protein
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靶点Dopamine Receptor
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受体D2|D3|5-HT2B
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研究领域others
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适应症Infertility
化学信息
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CAS Number81409-90-7
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分子量451.60
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分子式C26H37N5O2
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纯度>98% (HPLC)
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溶解度DMSO:32 mg/mL(70.86 mM)
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SMILES[H][C@@]12Cc3c[nH]c4cccc(c34)[C@@]1([H])C[C@H](CN2CC=C)C(=O)N(CCCN(C)C)C(=O)NCC
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Odaka H, et al. Cabergoline, dopamine D2 receptor agonist, prevents neuronal cell death under oxidative stress via reducing excitotoxicity. PLoS One. 2014 Jun 10;9(6):e99271.
产品手册
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