Literature DB >> 3858974

Structure activity relationships of substituted benzimidazoles.

A Brändström, P Lindberg, U Junggren.   

Abstract

The omeprazole molecule consists of three parts, a substituted pyridine ring, a substituted benzimidazole ring and CH2SO chain connecting the 2-positions of these ring systems. All three are essential for the antisecretory effect. In order to maintain a good effect the pyridine ring has to be substituted by alkyl or alkoxy groups, but not in the 6-position. The substituents in the benzimidazole ring are not that important, but substituents with strongly electron withdrawing groups such as NO2 or highly hydrophilic groups such as NHCOCH3 tend to give compounds with low antisecretory effects.

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Year:  1985        PMID: 3858974     DOI: 10.3109/00365528509095816

Source DB:  PubMed          Journal:  Scand J Gastroenterol Suppl        ISSN: 0085-5928


  3 in total

1.  Comparative bioavailability study of two oral omeprazole formulations after single and repeated administrations in healthy volunteers.

Authors:  T Duvauchelle; L Millerioux; V Gualano; E Evene; A Alcaide
Journal:  Clin Drug Investig       Date:  1998       Impact factor: 2.859

2.  Effects of NC-1300-B, a new benzimidazole derivative, on hog gastric H+, K+-ATPase, gastric acid secretion and HCl.ethanol-induced gastric lesions in rats.

Authors:  S Okabe; Y Akimoto; S Yamasaki; H Nagai
Journal:  Dig Dis Sci       Date:  1988-11       Impact factor: 3.199

Review 3.  Omeprazole. A preliminary review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in peptic ulcer disease and Zollinger-Ellison syndrome.

Authors:  S P Clissold; D M Campoli-Richards
Journal:  Drugs       Date:  1986-07       Impact factor: 9.546

  3 in total

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