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Dihydroorotate Dehydrogenase as a Target for the Development of Novel Helicobacter pylori-Specific Antimicrobials.
Ohishi, Tomokazu; Inaoka, Daniel Ken; Kita, Kiyoshi; Kawada, Manabu.
Afiliação
  • Ohishi T; Institute of Microbial Chemistry (BIKAKEN), Numazu, Microbial Chemistry Research Foundation.
  • Inaoka DK; School of Tropical Medicine and Global Health, Nagasaki University.
  • Kita K; School of Tropical Medicine and Global Health, Nagasaki University.
  • Kawada M; Institute of Microbial Chemistry (BIKAKEN), Numazu, Microbial Chemistry Research Foundation.
Chem Pharm Bull (Tokyo) ; 66(3): 239-242, 2018.
Article em En | MEDLINE | ID: mdl-29491257
ABSTRACT
Helicobacter pylori (H. pylori) infection is the world's most common bacterial infection, affecting approximately 50% of the global population. H. pylori is the strongest known risk factor for stomach diseases, including cancer. Hence, treatment for H. pylori infection can help reduce the risk of these diseases. However, the emergence of drug-resistant strains of H. pylori and the occurrence of adverse effects resulting from current therapies have complicated the successful eradication of H. pylori infection. Although various antibiotics that target several bacterial enzymes have been discovered, dihydroorotate dehydrogenase (DHODH) may hold potential for the development of novel anti-H. pylori agents with reduced toxicity and side effects. Here we review the existing literature that has focused on strategies for developing novel therapeutic agents that target the DHODH of H. pylori.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Helicobacter pylori / Oxirredutases atuantes sobre Doadores de Grupo CH-CH / Inibidores Enzimáticos / Antibacterianos Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Chem Pharm Bull (Tokyo) Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Helicobacter pylori / Oxirredutases atuantes sobre Doadores de Grupo CH-CH / Inibidores Enzimáticos / Antibacterianos Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Chem Pharm Bull (Tokyo) Ano de publicação: 2018 Tipo de documento: Article