• NNZ 2591 是环状甘氨酸脯氨酸 (cGP) 小肽的合成类似物 | MedChemExpress (MCE)


    NNZ 2591

    CAS:847952-38-9

    品牌:MedChemExpress (MCE)

    存储条件:Please store the product under the recommended conditions in the Certificate of Analysis.

    生物活性:NNZ 2591 是环状甘氨酸脯氨酸 (cGP) 小肽的合成类似物。NNZ 2591 具有口服活性并能穿过血脑屏障。NNZ 2591 在缺血性脑损伤后显示出神经保护作用。NNZ 2591 改善帕金森病大鼠模型的运动功能。NNZ 2591 具有研究缺血性脑损伤和天使综合征的潜力。

    体内:NNZ 2591 (30 mg/kg; p.o.) prevented scopolamine-induced memory impairment in rats[1]. NNZ 2591 (2, 20, 100 ng/rat; i.c.v.) shows neuroprotection in rats[2]. NNZ 2591 (3 mg/kg; s.c.; daily for 5 days) completely preventes brain damage and significantly reduces the L/R ratio of time taken to touch to the patch at 5 d after injury in rats[2]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: 4 months, male young adult Wistar rats[1]. Dosage: 30 mg/kg Administration: P.o.; 10 min after the (scopolamine) i.p. administration. Result: Significantly reduced the number of M2AchR positive neurons, significantly reduced the density of synaptophysin in the CA3 and CA4 sub-regions, and altered TH terminal staining in the striatum. Animal Model: 280-310 g adult male Wistar rats[2]. Dosage: 2, 20, 100 ng/rat Administration: I.c.v.; 2 h after HI injury Result: Reduced overall tissue damage in the sub-regions of the hippocampus, DG, cerebral cortex and the striatum. Animal Model: 280-310 g adult male Wistar rats[2]. Dosage: 3 mg/kg Administration: S.c.; daily for 5 days Result: Significantly reduced the median of tissue damage scores in the CA1-2, CA3 and CA4 sub-regions of the hippocampus, the DG.

    参考文献:

    [1]. Guan J, et al. NNZ-2591, a novel diketopiperazine, prevented scopolamine-induced acute memory impairment in the adult rat. Behav Brain Res. 2010 Jul 11;210(2):221-8.
    [2]. Guan J, et al. Peripheral administration of a novel diketopiperazine, NNZ 2591, prevents brain injury and improves somatosensory-motor function following hypoxia-ischemia in adult rats. Neuropharmacology. 2007 Nov;53(6):749-62.
    [3]. Copping NA, et al. Emerging Gene and Small Molecule Therapies for the Neurodevelopmental Disorder Angelman Syndrome. Neurotherapeutics. 2021 Jul;18(3):1535-1547.

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  • 原文地址:https://blog.csdn.net/mmmm12134/article/details/139406117