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首页-小分子抑制剂&激动剂-Cell Cycle/DNA Damage-Cyclin-dependent Kinase (CDK)-Cdk5 inhibitor 25-106
Cdk5 inhibitor 25-106

Chemical Structure : Cdk5 inhibitor 25-106

CAS No.:

Cdk5 inhibitor 25-106 (Compound 25-106)

货号: PC-47009Not For Human Use, Lab Use Only.

Cdk5 inhibitor 25-106 is a potent, brain-penetrant inhibitor of Cdk5/p35 activity with IC50 of 178 nM.

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25 mg Get quote
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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

    生物&药学活性

    Cdk5 inhibitor 25-106 is a potent, brain-penetrant inhibitor of Cdk5/p35 activity with IC50 of 178 nM.
    Cdk5 inhibitor 25-106 demonstrated similar inhibition against highly homologous Cdk2/Cyclin E (IC50=149 nM), and weak inhibition against CDK9/Cyclin T1 (IC50=5710 nM) in in vitro selectivity assays.
    25-106 significantly reduced phospho-Ser549 synapsin I levels in the striatum 2 h after I.V. injection.
    25-106 inhibits Cdk5 activity in vivo and displays high potency for inhibition in vitro.
    25-106 (50 mg/kg) displayed an increased latency to suspend immobility and displayed a reduction in total immobility time as compared to vehicle-injected mice, modulated behavioral phenotypes linked to Cdk5 through previous characterizations of conditional knockout mice.

    物理化学性质&存储条件

    分子量 345.399
    分子式 C18H23N3O4
    外观性状 Solid
    CAS No.
    储存条件
    固体粉末
    -20°C 12 个月; 4°C 6 个月
    配置液
    -80°C 6 个月; -20°C 6 个月
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    N-(5-cyclobutyl-1H-pyrazol-3-yl)-2-(3,4,5-trimethoxyphenyl)acetamide

    参考文献

    1. Umfress A, et al. Front Pharmacol. 2022 May 12;13:863762.

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