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目錄:MedChemExpress LLC>>信號(hào)通路>> SH5-07 | MedChemExpress

SH5-07 | MedChemExpress
  • SH5-07 | MedChemExpress
參考價(jià) 2060
具體成交價(jià)以合同協(xié)議為準(zhǔn)
參考價(jià) 2060
具體成交價(jià)以合同協(xié)議為準(zhǔn)
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更新時(shí)間:2023-09-28 14:55:31瀏覽次數(shù):122評(píng)價(jià)

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CAS 1456632-41-9 純度 ≥98.0%
分子量 625.61 分子式 C??H??F?N?O?S
供貨周期 現(xiàn)貨 規(guī)格 10 mM * 1 mL
貨號(hào) HY-100494 應(yīng)用領(lǐng)域 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥
SH5-07 是一種基于異羥肟酸的 <b>Stat3</b> 抑制劑,在體外實(shí)驗(yàn)中的 <b>IC<sub>50</sub></b> 值為 3.9 μM<sup>[1]</sup>。

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SH5-07

CAS No. : 1456632-41-9

MCE 國(guó)際站:SH5-07

產(chǎn)品活性:SH5-07 是一種基于異羥肟酸的 Stat3 抑制劑,在體外實(shí)驗(yàn)中的 IC50 值為 3.9 μM。

研究領(lǐng)域:JAK/STAT Signaling  |  Stem Cell/Wnt

作用靶點(diǎn):STAT

In Vitro: SH5-07 is a hydroxamic acid analog of BP-1-102. SH5-07 dose-dependently inhibits Stat3 activity with an IC50 of 3.9±0.6 μM in in vitro assay. It preferentially inhibits Stat3:Stat3 DNA-binding activity, ahead of inhibiting Stat1:Stat3 activity, with minimal effects on Stat1:Stat1 activity. SH5-07 binds Stat3, disrupts Stat3 association with growth factor receptor, and thereby inhibits Stat3 phosphorylation. It induces antitumor cell effects against malignant cells harboring constitutively-active Stat3. SH5-07 inhibits the expression of known Stat3-regulated genes. Bcl-2, Bcl-xL, c-Myc, Survivin, Cyclin D1 and Mcl-1 expression is reduced in response to 24 h, 5 μM SH5-07 treatment.

In Vivo: Tail vein injection or oral gavage delivery of SH5-07 or SH4-54 inhibits growth of 90-150 mm3 established subcutaneous mouse xenografts of human glioma (U251MG) and breast (MDA-MB-231) tumors that harbor aberrantly-active Stat3, associated with decreased c-Myc, Mcl-1 and Cyclin D1 expression. No significant changes in body weights, blood cell counts, or the gross anatomy of organs, or obvious signs of toxicity are observed.

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