Omberacetam (Synonyms: N-(1-(苯基乙酰基)-L-脯氨酰)甘氨酸乙酯; GVS-111; SGS-111)
目录号: PL04722 纯度: ≥99%
CAS No. :157115-85-0
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中文名称
Omberacetam
中文别名
N-(1-(苯基乙酰基)-L-脯氨酰)甘氨酸乙酯;N-(1-(苯基乙酰基)-L-脯氨酰)甘氨酸乙酯(Noopept);Noopept(GVS-111) 抑制剂;苯乙酰甘氨酸乙酯;N-(1-(苯基乙酰基)-L-脯氨酰)甘氨酸乙酯生产厂家
英文名称
Omberacetam
英文别名
Noopept;(S)-Ethyl 2-(1-(2-phenylacetyl)pyrrolidine-2-carboxamido)acetate;ethyl 2-[[(2S)-1-(2-phenylacetyl)pyrrolidine-2-carbonyl]amino]acetate;N-(1-(Phenylacetyl)-L-prolyl)glycine ethyl ester;1-(2-Phenylacetyl)-L;1-(2-Phenylacetyl)-L-prolylglycine Ethyl Ester;N-Phenylacetyl-L-prolylglycine ethyl ester;GVS111;GVS-111;Omberacetam;SGS 111;SGS-111;NOOPEPT(GVS-111);1-(2-Phenylacetyl)-L-prolyl-glycine ethyl ester;Ethyl N-[1-(Phenylacetyl)-L-prolyl]glycinate;N-[1-(Phenylacetyl)-L-prolyl]glycine Ethyl Ester;skype;Noopept,N-Phenylacetyl-L-Prolylglycine ethyl ester
Cas No.
157115-85-0
分子式
C17H22N2O4
分子量
318.37
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
Omberacetam (GVS-111) 是可作为膳食补充剂的多肽。
生物活性
Omberacetam (GVS-111) is a medication promoted and prescribed in Russia and neighbouring countries as a nootropic.
性状
Solid
体外研究(In Vitro)
Nooglutil exhibits pharmacologically significant competition with a selective agonist of AMPA receptors ([G-3H]Ro 48-8587) for the receptor binding sites (with IC50 = 6.4 +/- 0.2 microM), while the competition of noopept for these receptor binding sites was lower by an order of magnitude (IC50 = 80 +/- 5.6 microM) [1]. GVS-111 significantly increased neuronal survival after H(2)O(2)-treatment displaying a dose-dependent neuroprotective activity from 10 nM to 100 microM, and an IC(50) value of 1.21+/-0.07 microM. GVS-111 inhibited the accumulation of intracellular free radicals and lipid peroxidation damage in neurons treated with H(2)O(2) or FeSO(4), suggesting an antioxidant mechanism of action [2]. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
N-Phenylacetyl-L-prolylglycine ethyl ester (GVS-111) administered intravenously at a dose of 0.5 mg/kg/day, for the first time 1 h after ischaemic lesion and then for 9 post-operative days, with the last administration 15 min before testing, attenuated the deficit [3]. GVS-111 itself was not found in rat brain 1 h after 5 mg/kg i.p. administration up to limit of detection (LOD) under high performance liquid chromatography (HPLC) conditions [4]. The most pronounced antiinflammatory effect of dipeptide was observed on the model of adjuvant arthritis in rats, where the drug administered over 25 days in a daily dose of 0.5 mg/kg (i.m.) or 5 mg/kg (p.o.) significantly reduced the chronic immune inflammation (on the 12th day, by 94.0 and 74.1%, respectively) [5]. has not independently confirmed the accuracy of these methods.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Firstova IuIu, et al. Studying specific effects of nootropic drugs on glutamate receptors in the rat brain. Eksp Klin Farmakol. 2011;74(1):6-10.
[2]. Pelsman A, et al. GVS-111 prevents oxidative damage and apoptosis in normal and Downs syndrome human cortical neurons. Int J Dev Neurosci. 2003 May;21(3):117-24.
溶解度数据
In Vitro: DMSO : ≥ 100 mg/mL (314.10 mM)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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