
Rabeprazole
CAS No. 117976-89-3
Rabeprazole ( —— )
产品货号. M33636 CAS No. 117976-89-3
Rabeprazole (LY307640) 是一种二代质子泵抑制剂 (pump inhibitor, PPI),不可逆地抑制胃 H+/K+-ATPase。Rabeprazole 诱导细胞凋亡 (apoptosis)。Rabeprazole 也抑制尿苷核苷核糖水解酶 (UNH) ,IC50 为 0.3 μM。Rabeprazole 可用于胃溃疡和胃食管反流的研究。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥250 | 有现货 |
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10MG | ¥388 | 有现货 |
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25MG | ¥602 | 有现货 |
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50MG | ¥884 | 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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生物学信息
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产品名称Rabeprazole
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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Rabeprazole (LY307640) 是一种二代质子泵抑制剂 (pump inhibitor, PPI),不可逆地抑制胃 H+/K+-ATPase。Rabeprazole 诱导细胞凋亡 (apoptosis)。Rabeprazole 也抑制尿苷核苷核糖水解酶 (UNH) ,IC50 为 0.3 μM。Rabeprazole 可用于胃溃疡和胃食管反流的研究。
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产品描述Rabeprazole (LY307640) is a second-generation proton pump inhibitor (PPI) that irreversibly inactivates gastric H+/K+-ATPase. Rabeprazole induces apoptosis. Rabeprazole acts as an uridine nucleoside ribohydrolase (UNH) inhibitor with an IC50 of 0.3 μM. Rabeprazole can be used for the research of gastric ulcerations and gastroesophageal reflux.
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体外实验Rabeprazole attenuates the cell viability of the human gastric cancer cells following treatment with 0.2 mM for 16 hours.Rabeprazole completely inhibits the phosphorylation of ERK1/2 in the MKN-28 cells. The gastric cancer cell line MKN-28 is cultured in acidic culture media (pH 5.4) for 2 hours. Pretreatment with Rabeprazole (0.2 mM for 2 hours) leads to strong inhibition of ERK1/2 phosphorylation in the MKN-28 cells.Cell Viability Assay Cell Line:Three gastric cancer cell lines KATO III, MKN-28 and MKN-45 Concentration:0.2 mM Incubation Time:16 hours Result:Treatment resulted in the attenuation of viability in all cancer cell lines tested, the cell viability of the MKN-28 cells significantly decreased compared with the KATO III and MKN-45 cells, respectively. Cell Viability Assay Cell Line:Three gastric cancer cell lines (KATO III, MKN-28 and MKN-45) Concentration: 0.2 mM Incubation Time:Pretreatment for 2 hours Result:Led to strong inhibition of ERK 1/2 phosphorylation in the MKN-28 cells, but a similar effect was not observed in the KATO III and MKN-45 cells.
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体内实验Rabeprazole (10 mg/kg; P.O.; every 48 h for 18 weeks) course leads to a significant decline in bone mineral density (BMD) and decreases serum calcium level and produces secondary hyperparathyroidism in female mice.Animal Model:Female Swiss albino mice (body weight equals 18-26 g) Dosage:10 mg/kg Administration:Oral administration; every 48 h for 18 weeks Result:Showed significantly lower serum calcium level compared to the vehicle treated group (5.5±2.07 vs. 9.68±2.77).
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同义词——
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通路Cell Cycle/DNA Damage
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靶点Potassium Channel
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受体Potassium Channel | STAT
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研究领域——
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适应症——
化学信息
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CAS Number117976-89-3
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分子量359.44
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分子式C18H21N3O3S
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纯度>98% (HPLC)
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溶解度——
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SMILESCOCCCOc1ccnc(CS(=O)c2nc3ccccc3[nH]2)c1C
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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. Tara A Shea, et al.Identification of Proton-Pump Inhibitor Drugs That Inhibit Trichomonas Vaginalis Uridine Nucleoside Ribohydrolase. Bioorg Med Chem Lett. 2014 Feb 15;24(4):1080-4.?
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