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omeprazole and Chromosome-Defective Micronuclei

omeprazole has been researched along with Chromosome-Defective Micronuclei in 1 studies

Omeprazole: A 4-methoxy-3,5-dimethylpyridyl, 5-methoxybenzimidazole derivative of timoprazole that is used in the therapy of STOMACH ULCERS and ZOLLINGER-ELLISON SYNDROME. The drug inhibits an H(+)-K(+)-EXCHANGING ATPASE which is found in GASTRIC PARIETAL CELLS.
omeprazole : A racemate comprising equimolar amounts of (R)- and (S)-omeprazole.
5-methoxy-2-{[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]sulfinyl}-1H-benzimidazole : A member of the class of benzimidazoles that is 1H-benzimidazole which is substituted by a [4-methoxy-3,5-dimethylpyridin-2-yl)methyl]sulfinyl group at position 2 and a methoxy group at position 5.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Sinués, B1
Fanlo, A1
Bernal, ML1
Val, M1
Mayayo, E1

Trials

1 trial available for omeprazole and Chromosome-Defective Micronuclei

ArticleYear
Omeprazole treatment: genotoxicity biomarkers, and potential to induce CYP1A2 activity in humans.
    Human & experimental toxicology, 2004, Volume: 23, Issue:3

    Topics: Adolescent; Adult; Anti-Ulcer Agents; Aryl Hydrocarbon Hydroxylases; Caffeine; Cell Division; Chromo

2004