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Linaprazan Linaprazan (AZD0865) can inhibit H+,K+ -ATPase in the stomach through K+ competitive binding, ( IC 50 : 1.0 ± 0.2 μM), it has a strong inhibitory effect on acid. Linaprazan (AZD0865) can be used for research on reflux esophagitis with oral activity [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AZD0865. CAS No. 248919-64-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100412. MedChemExpress MCE
Linaprazan Linaprazan is an acid-suppressing compound with a rapid onset of action and potent acid inhibition. It inhibits gastric H+, K+-ATPase by K+-competitive binding. Synonyms: Imidazo[1,2-a]pyridine-6-carboxamide, 8-[[(2,6-dimethylphenyl)methyl]amino]-N-(2-hydroxyethyl)-2,3-dimethyl-; 2, 3-Dimethyl-8-[ (2, 6-dimethylbenzyl) amino]-6-[N- (2-hydroxyethyl) aminocarbonyl]imidazo[1, 2-a]pyridine; AZD 0865; AZD-0865; AZD0865; 8-((2,6-dimethylbenzyl)amino)-N-(2-hydroxyethyl)-2,3-dimethylimidazo[1,2-a]pyridine-6-carboxamide. Grades: 98%. CAS No. 248919-64-4. Molecular formula: C21H26N4O2. Mole weight: 366.46. BOC Sciences 10
Linaprazan Linaprazan. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Linaprazan. Product Category: Heterocyclic Organic Compound. CAS No. 248919-64-4. Product ID: ACM248919644. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry. 4
Linaprazan glurate Linaprazan glurate inhibits exogenously or endogenously stimulated gastric acid secretion. Linaprazan glurate exhibits several advantageous properties, such as fast onset, high in vivo potency and/or long duration of action. Linaprazan glurate is useful in the research of gastrointestinal inflammatory diseases and peptic ulcer diseases (extracted from patent WO2010063876A1) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: X842. CAS No. 1228559-81-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145578. MedChemExpress MCE
Linaprazan mesylate Linaprazan can inhibit gastric H(+),K(+)-ATPase activity (IC 50: 1.0 ± 0.2 μM) and acid formation in vitro. Phase II clinical trials for the treatment of Gastroesophageal reflux disease (GERD) were discontinued. Uses: Gastroesophageal reflux disease (gerd). Synonyms: AR-h044277AW; AZD-0865 mesilate; AZD 0865 mesilate; AZD0865 mesilate; AZD-0865 mesylate; AZD 0865 mesylate; AZD0865 mesylate; Linaprazan mesilate; 8-((2,6-dimethylbenzyl)amino)-N-(2-hydroxyethyl)-2,3-dimethylimidazo[1,2-a]pyridine-6-carboxamide methanesulfonate;248919-64-4(base). Grades: 98%. CAS No. 855998-67-3. Molecular formula: C22H30N4O5S. Mole weight: 462.57. BOC Sciences 10

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