SH-4-54
CAS No. 1456632-40-8
SH-4-54 ( SH-4-54 | SH 4-54 | SH4-54 | SH-454 | SH 454 | SH454. )
产品货号. M11971 CAS No. 1456632-40-8
一种有效的 BBB 渗透性非磷酸化 STAT3 抑制剂,可与 STAT3 蛋白强烈结合,Kd 为 300 nM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥938 | 有现货 |
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| 10MG | ¥1568 | 有现货 |
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| 25MG | ¥2771 | 有现货 |
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| 50MG | ¥4166 | 有现货 |
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| 100MG | ¥5652 | 有现货 |
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| 200MG | ¥7641 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥1321 | 有现货 |
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生物学信息
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产品名称SH-4-54
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述一种有效的 BBB 渗透性非磷酸化 STAT3 抑制剂,可与 STAT3 蛋白强烈结合,Kd 为 300 nM。
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产品描述A potent, BBB permeable, nonphosphorylated STAT3 inhibitor that strongly binds to STAT3 protein with Kd of 300 nM; potently kills glioblastoma brain cancer stem cells (BTSCs) and effectively suppresses STAT3 phosphorylation and its downstream transcriptional targets at low nM concentrations; potently suppresses glioma tumor growth, and inhibits pSTAT3 in vivo.(In Vitro):SH-4-54 potently kills glioblastoma brain cancer stem cells (BTSCs) and effectively suppresses STAT3 phosphorylation and its downstream transcriptional targets at low nM concentrations.SH-4-54 shows unprecedented cytotoxicity in human BTSCs, displays no toxicity in human fetal astrocytes, potently suppresses pSTAT3 with nanomolar IC50s, inhibiting STAT3's downstream targets, and shows no discernible off-target effects at therapeutic doses.(In Vivo):SH-4-54 exhibits blood-brain barrier permeability potently controls glioma tumor growth, and inhibits pSTAT3 in vivo. SH-4-54 demonstrates the power of STAT3 inhibitors for the treatment of BTSCs and validates the therapeutic efficacy of a STAT3 inhibitor for GBM clinical application.SH-4-54 decreases pSTAT3 expression in tumor cells of treated mice. SH-4-54 appears to decrease proliferation and increase apoptosis of treated tumors.
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体外实验SH-4-54 potently kills glioblastoma brain cancer stem cells (BTSCs) and effectively suppresses STAT3 phosphorylation and its downstream transcriptional targets at low nM concentrations.SH-4-54 shows unprecedented cytotoxicity in human BTSCs, displays no toxicity in human fetal astrocytes, potently suppresses pSTAT3 with nanomolar IC50s, inhibiting STAT3's downstream targets, and shows no discernible off-target effects at therapeutic doses.
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体内实验SH-4-54 exhibits blood-brain barrier permeability potently controls glioma tumor growth, and inhibits pSTAT3 in vivo. SH-4-54 demonstrates the power of STAT3 inhibitors for the treatment of BTSCs and validates the therapeutic efficacy of a STAT3 inhibitor for GBM clinical application.SH-4-54 decreases pSTAT3 expression in tumor cells of treated mice. SH-4-54 appears to decrease proliferation and increase apoptosis of treated tumors.
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同义词SH-4-54 | SH 4-54 | SH4-54 | SH-454 | SH 454 | SH454.
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通路JAK/STAT Signaling
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靶点STAT
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受体STAT3|STAT5
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研究领域Cancer
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适应症——
化学信息
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CAS Number1456632-40-8
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分子量610.5921
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分子式C29H27F5N2O5S
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纯度>98% (HPLC)
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溶解度10 mM in DMSO
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SMILESO=C(O)C1=CC=C(N(CC2=CC=C(C3CCCCC3)C=C2)C(CN(C)S(=O)(C4=C(F)C(F)=C(F)C(F)=C4F)=O)=O)C=C1
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化学全称Benzoic acid, 4-[[(4-cyclohexylphenyl)methyl][2-[methyl[(2,3,4,5,6-pentafluorophenyl)sulfonyl]amino]acetyl]amino]-
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Haftchenary S, et al. ACS Med Chem Lett. 2013 Sep 8;4(11):1102-7.
2. Arpin CC, et al. Mol Cancer Ther. 2016 May;15(5):794-805.
3. Linher-Melville K, et al. PLoS One. 2016 Aug 11;11(8):e0161202.
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