OmberacetamN-(1-(苯基乙酰基)-L-脯氨酰)甘氨酸乙酯,157115-85-0

OmberacetamN-(1-(苯基乙酰基)-L-脯氨酰)

甘氨酸乙酯,157115-85-0
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  • HY-17456
  • 2025年12月05日
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    • 详细信息
    • 技术资料
    • 保存条件

      Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.

    • 英文名

      GVS-111; SGS-111

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • CAS号

      157115-85-0

    • 规格

      10 mM * 1 mL/5 mg/10 mg/25 mg/50 mg/100 mg

    规格:10 mM * 1 mL产品价格:¥418.0
    规格:5 mg产品价格:¥380.0
    规格:10 mg产品价格:¥500.0
    规格:25 mg产品价格:¥900.0
    规格:50 mg产品价格:¥1500.0
    规格:100 mg产品价格:¥2500.0

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    Omberacetam

    CAS No. : 157115-85-0

    MCE 国际站:Omberacetam

    产品活性:Omberacetam (GVS-111) 是可作为膳食补充剂的多肽。

    研究领域:Membrane Transporter/Ion Channel  |  Neuronal Signaling

    作用靶点:iGluR

    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].

    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].

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    OmberacetamN-(1-(苯基乙酰基)-L-脯氨酰)甘氨酸乙酯,157115-85-0
    ¥380 - 2500