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CAS No. :

MCE 國(guó)際站：Synucleozid hydrochloride

產(chǎn)品活性：Synucleozid (NSC 377363) 是可編碼 α-突觸核蛋白的 SNCA mRNA 的有效抑制劑 (IC₅₀=1.5 μM)。Synucleozid 選擇性靶向 α-synuclein mRNA 的 5'UTR的 IRE 位點(diǎn)，減少了加載到多核糖體中的 SNCA mRNA 的量，從而抑制了α-synuclein 蛋白的翻譯。Synucleozid 有潛力用于帕金森病的相關(guān)研究。

研究領(lǐng)域：Cell Cycle/DNA Damage

作用靶點(diǎn)：DNA/RNA Synthesis

In Vitro: Synucleozid (0.25-1 μM; 24 hours) abrogates cytotoxicity induced by α-synuclein preformed fibrils, which act as seeds and recruit endogenous α-synuclein to aggregate.
Synucleozid (0-1 μM; 24 hours) binds to the A bulge near the base of the IRE hairpin, reduced levels of α-synuclein in a dose-dependent manner with an IC₅₀ of 500 nM, and inhibits α-synuclein protein expression in SH-SY5Y neuroblastoma cells.
Synucleozid (100 nM-100 μM; 24 hours) binds to 2-AP-labeled and native IRE RNA with similar affinities. It decreases 2-AP emission with an EC₅₀ value of 2.7 μM, recovery of 2-AP emissions is observed as a function of unlabeled SNCA IRE RNA (RNA-0) concentration, affording a competitive K_d of 1.5 μM.
Synucleozid (0.25-1 μM; 24 hours) decreases α-synuclein and other proteins that have IREs in their mRNA’s UTR including APP, PrP, Ferritin and TfR as a dose-dependent mannner. All panels is completed in SH-SY5Y cells, except for PrP protein which is assessed in Neuro-2A cells.

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