N-Oleoyl glycine
CAS No. 2601-90-3
N-Oleoyl glycine ( —— )
产品货号. M26577 CAS No. 2601-90-3
N-油酰甘氨酸是一种脂肪氨基酸,能够通过激活 CB1 受体和增强胰岛素介导的 Akt 信号通路来促进 3T3-L1 脂肪生成。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥316 | 有现货 |
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| 10MG | ¥518 | 有现货 |
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| 25MG | ¥794 | 有现货 |
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| 50MG | ¥1239 | 有现货 |
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| 100MG | ¥1855 | 有现货 |
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| 200MG | ¥2770 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称N-Oleoyl glycine
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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N-油酰甘氨酸是一种脂肪氨基酸,能够通过激活 CB1 受体和增强胰岛素介导的 Akt 信号通路来促进 3T3-L1 脂肪生成。
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产品描述N-Oleoyl glycine, a lipoamino acid, was able to promote 3T3-L1 adipogenesis through the activation of CB1 receptor and the enhancement of insulin-mediated Akt signaling pathway.(In Vitro):N-Oleoyl glycine stimulated lipid accumulation and significantly increased adipogenic genes (PPARγ and aP2), in a dose- and time-dependent manner.?Additionally, N-Oleoyl glycine markedly increased the mRNA expression of CB1 receptor and the inhibition of CB1R by its antagonist SR141716 abolished the promotive effects of N-Oleoyl glycine on lipid accumulation and the protein expression of PPARγ and aP2.?Furthermore, N-Oleoyl glycine increased the ratio of p-Akt/Akt and p-FoxO1/FoxO1, which could be reversed by SR141716.?Moreover, N-Oleoyl glycine-induced enhancement of adipogenesis, activation of insulin-mediated Akt signaling pathway and inactivation of FoxO1 were effectively blocked by Wortmannin, a specific PI3K/Akt inhibitor, indicating the essential role of Akt signaling pathway in the process of N-Oleoyl glycine-stimulated 3T3-L1 adipogenesis.
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体外实验N-Oleoyl glycine is a lipoamino acid, which stimulates adipogenesis associated with activation of CB1 receptor and Akt signaling pathway in 3T3-L1 adipocyte. N-Oleoyl glycine (1, 5, 10, 20, 50 μM) dose- and time-dependently stimulates 3T3-L1 adipogenesis after treatment for 1-10 days via activation of CB1R. N-Oleoyl glycine also elevates Akt signaling pathway during the differentiation of 3T3-L1 adipocytes.
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体内实验——
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同义词——
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通路GPCR/G Protein
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靶点Cannabinoid Receptor
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受体CYP3A
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研究领域——
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适应症——
化学信息
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CAS Number2601-90-3
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分子量339.52
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分子式C20H37NO3
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (294.54 mM)
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SMILESCCCCCCCC\C=C/CCCCCCCC(=O)NCC(O)=O
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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.Method for increasing HDL cholesterol levels?using?heteroaromatic phenylmethanes. United States Patent 6103733
021-51111890
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