
Isoangustone A
CAS No. 129280-34-8
Isoangustone A ( —— )
产品货号. M31517 CAS No. 129280-34-8
Isoangustone A has antitumor activity, it can induce G1 cycle arrest in DU145 human prostate and 4T1 murine mammary cancer cells, it inhibits cell proliferation by targeting PI3K, MKK4, and MKK7 in human melanoma.
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥4040 | 有现货 |
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50MG | 获取报价 | 有现货 |
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100MG | 获取报价 | 有现货 |
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生物学信息
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产品名称Isoangustone A
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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Isoangustone A has antitumor activity, it can induce G1 cycle arrest in DU145 human prostate and 4T1 murine mammary cancer cells, it inhibits cell proliferation by targeting PI3K, MKK4, and MKK7 in human melanoma.
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产品描述Isoangustone A has antitumor activity, it can induce G1 cycle arrest in DU145 human prostate and 4T1 murine mammary cancer cells, it inhibits cell proliferation by targeting PI3K, MKK4, and MKK7 in human melanoma. Isoangustone A dampens mesangial sclerosis associated with inflammation in response to high glucose through hindering TGF-β and NF-?oB signaling. Isoangustone A also shows strong ferric reducing activities and effectively scavenged DPPH, ABTS(+), and singlet oxygen radicals.
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体外实验Cell Proliferation Assay Cell Line:SK-MEL-28 Concentration:10 and 20 μM Incubation Time:48 and 72 h Result:Inhibited proliferation in a dose- and time-dependent manner.Cell Cycle Analysis Cell Line:SK-MEL-28 Concentration: 10 and 20 μM Incubation Time:48 h Result:Caused cell cycle arrest at G1 phase.Western Blot Analysis Cell Line:SK-MEL-28 Concentration:10 and 20 μM Incubation Time:48 h Result:Inhibited the expression of cyclin D1 and cyclin E. Suppressed phosphorylation of Rb in a dose-dependent manner. Inhibited the phosphorylation of Akt (Ser473, Thr308) and GSK3β (Ser9). Suppressed the phosphorylation of JNK1/2, but had no effect on ERK1/2 or p38.Cell Autophagy Assay Cell Line:SW480 cells Concentration:20 μM Incubation Time:0.5, 2 and 4 h Result:Deformed mitochondria, nondegradable cellular debris were all observable together with autophagic vacuoles in cells after 4 h.Apoptosis Analysis Cell Line:SW480 cells Concentration:15 μM Incubation Time:6 hResult:Induced elevation of apoptotic Annexin V+/PI- and Annexin V+/PI+ cell populations.
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体内实验Animal Model:Male Balb/c nu/nu mice, SK-MEL-28 xenograft modelDosage:2 or 10 mg/kg Administration:Intraperitoneal injection, daily for 35 days Result:Significantly suppressed tumor weight compared to the control group. Markedly inhibited the expression of proliferating cell nuclear antigen (PCNA). Decreased phosphorylation levels of Akt.
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同义词——
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通路Others
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靶点Other Targets
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受体——
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研究领域——
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适应症——
化学信息
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CAS Number129280-34-8
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分子量422.47
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分子式C25H26O6
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纯度>98% (HPLC)
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溶解度——
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SMILES——
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化学全称——
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
产品手册




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