
Ceranib1
CAS No. 328076-61-5
Ceranib1 ( —— )
产品货号. M26103 CAS No. 328076-61-5
Ceranib1 是神经酰胺酶的抑制剂。它可以抑制卵巢癌细胞的增殖。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥786 | 有现货 |
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5MG | ¥1175 | 有现货 |
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10MG | ¥1434 | 有现货 |
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25MG | ¥3183 | 有现货 |
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50MG | ¥4747 | 有现货 |
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100MG | ¥6788 | 有现货 |
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500MG | ¥13932 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Ceranib1
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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Ceranib1 是神经酰胺酶的抑制剂。它可以抑制卵巢癌细胞的增殖。
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产品描述Ceranib1 is an inhibitor of ceramidase. It inhibits the proliferation of ovarian cancer cells. Ceranib1 inhibits ceramidase activity toward an exogenous ceramide analog, induces the accumulation of multiple ceramide species, decreases levels of S1P and sphingosine.(In Vitro):Ceranib1 produces a dose-dependent decrease in ceramidase activity, with 50% inhibition at 55 and 28 μM in SKOV3 cells. Ceranib1 prevents the hydrolysis of endogenous ceramide species and reduces intracellular sphingosine and S1P. Ceranib1 (10 nM-10 μM; 72 hours) exhibits antiproliferative activity for SKOV3 cells. Ceranib1 (24 hours) does not cause significant acute cytotoxicity at concentrations up to at least those used in the ceramidase assay in SKOV3 cells.
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体外实验Ceranib1 produces a dose-dependent decrease in ceramidase activity, with 50% inhibition at 55 and 28 μM in SKOV3 cells.Ceranib1 (24 hours) does not cause significant acute cytotoxicity at concentrations up to at least those used in the ceramidase assay in SKOV3 cells.Ceranib1 prevents the hydrolysis of endogenous ceramide species and reduces intracellular sphingosine and S1P.Ceranib1 (10 nM-10 μM; 72 hours) exhibits antiproliferative activity for SKOV3 cells. Cell Proliferation Assay Cell Line:SKOV3 cellsConcentration:10 nM-10 μM (varying concentrations)Incubation Time:72 hours Result:Inhibited cell proliferation with IC50 values of 3.9 ± 0.3 μM.
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体内实验——
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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PROTAC Linker
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研究领域——
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适应症——
化学信息
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CAS Number328076-61-5
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分子量395.458
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分子式C26H21NO3
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纯度>98% (HPLC)
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溶解度——
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SMILESCOc1ccc(\C=C\C(=O)c2c(-c3ccccc3)c3cc(C)ccc3[nH]c2=O)cc1
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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
1.Khan S, et al. A selective BCL-XL PROTAC degrader achieves safe and potent antitumor activity. Nat Med. 2019 Dec;25(12):1938-1947.
产品手册




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