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View all H<sup>+</sup>,K<sup>+</sup>-ATPase products.Omeprazole is a H+,K+-ATPase inhibitor (IC50 = 5.8 μM) that displays antisecretory and antiulcer activity. Inhibits gastric acid secretion (IC50 = 0.16 μM for histamine-induced acid formation) and reduces gastric lesion formation induced by a variety of ulcerative stimuli. Antibacteral against Helicobacter pylori in vitro. Also inhibits CYP2C19, CYP2C9 and CYP3A (Ki values are 3.1, 40.1 and 84.4 μM respectively) and blocks swelling-dependent chloride channels (ICIswell). Enhances anti-SARS-CoV-2 acitvity of Remdesivir and Aprotinin (Cat. No. 4139).
分子量 | 345.42 |
公式 | C17H19N3O3S |
储存 | Desiccate at +4°C |
纯度 | ≥99% (HPLC) |
CAS Number | 73590-58-6 |
PubChem ID | 4594 |
InChI Key | SUBDBMMJDZJVOS-UHFFFAOYSA-N |
Smiles | COC1=CC=C2N=C(NC2=C1)S(=O)CC1=C(C)C(OC)=C(C)C=N1 |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
参考文献是支持产品生物活性的出版物。
Satoh et al (1989) Antisecretory and anitulcer activities of a novel proton pump inhibitor AG-1749 in dogs and rats. J.Pharmacol.Exp.Ther. 248 806 PMID: 2537418
Richardson et al (1998) Proton pump inhibitors. Drugs 56 307 PMID: 9777309
Schmarda et al (2000) The gastric H,K-ATPase blocker lansoprazole is an inhibitor of chloride channels. Br.J.Pharmacol. 129 598 PMID: 10711360
Bojkova et al (2020) SARS-CoV-2 and SARS-CoV differ in their cell tropism and drug sensitivity profiles. BioRxiv - Paper not yet peer reviewed.
关键词: Omeprazole, Omeprazole supplier, H+K+-ATPase, inhibitors, inhibits, Hydrogen, Potassium-ATPase, Ion, Transporters, Pumps, ATPases, cytochrome, p450, CYP2C19, CYP2C9, CYP3A, SARS-CoV-2, COVID-19, severe, acute, respiratory, syndrome, H+,K+-ATPase, Cytochrome, P450, Coronavirus, 2583, Tocris Bioscience
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We use it in the pharmacology lab for the assigment experiments
We prepare the solutions the same day of use