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Rabeprazole sodium (Habeprazole Sodium) 是一种质子泵抑制剂,不可逆地抑制胃 H+/K+-ATPase,可研究胃溃疡和胃食管反流。它诱导细胞凋亡,也抑制尿苷核苷核糖水解酶 ,IC50为 0.3 μM。
Rabeprazole sodium (Habeprazole Sodium) 是一种质子泵抑制剂,不可逆地抑制胃 H+/K+-ATPase,可研究胃溃疡和胃食管反流。它诱导细胞凋亡,也抑制尿苷核苷核糖水解酶 ,IC50为 0.3 μM。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
5 mg | ¥ 255 | 现货 | |
10 mg | ¥ 413 | 现货 | |
25 mg | ¥ 618 | 现货 | |
50 mg | ¥ 763 | 现货 | |
100 mg | ¥ 1,120 | 现货 | |
200 mg | ¥ 1,670 | 现货 | |
500 mg | ¥ 2,820 | 期货 | |
1 mL x 10 mM (in DMSO) | ¥ 455 | 现货 |
产品描述 | Rabeprazole sodium (Habeprazole Sodium) is a 4-(3-methoxypropoxy)-3-methylpyridinyl derivative of timoprazole that is used in the therapy of stomach ulcers and Zollinger-Ellison syndrome. The drug inhibits H(+)-K(+)-exchanging ATPase which is found in gastric parietal cells. |
靶点活性 | UNH:0.3 μM (IC50) |
体外活性 | 给予rabeprazole显著降低了MKN-28细胞的活力。rabeprazole的暴露显著诱导AGS细胞发生凋亡。rabeprazole完全抑制了MKN-28细胞中ERK 1/2的磷酸化,而在KATO III或MKN-45细胞中未观察到同样的效果。rabeprazole能有效抑制胃癌细胞中ERK 1/2的磷酸化。因此,rabeprazole通过失活ERK1/2信号通路,能减弱人类胃癌细胞的细胞活力[2]。 |
体内活性 | Rabeprazole似乎不会加剧胃切除大鼠的骨代谢障碍,反而缓解了TG诱导的BMD下降[1]。 |
细胞实验 | Rabeprazole is administrated to three gastric cancer cell lines, KATO III, MKN-28 and MKN-45, at a dosage of 0.2 mM for 16 h. The viability of these cells is determined by a trypan blue exclusion assay.(Only for Reference) |
别名 | 雷贝拉唑钠, Rebeprazole sodium, LY307640 sodium, Habeprazole Sodium, Dexrabeprazole Sodium, Aciphex Sodium |
分子量 | 381.42 |
分子式 | C18H20N3NaO3S |
CAS No. | 117976-90-6 |
Smiles | c12c([n-]c(n1)S(=O)Cc1c(c(ccn1)OCCCOC)C)cccc2.[Na+] |
密度 | 0.45~0.55 g/ml |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 58.82 mg/mL (154.21 mM), Sonication is recommended. H2O: 1.34 mg/mL (3.5 mM), Sonication is recommended. Ethanol: 71 mg/mL (186.1 mM) | ||||||||||||||||||||||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||||||||||||||||||||||
H2O/DMSO/Ethanol
DMSO/Ethanol
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