Metabolism of Some Drugs Which Contain Carbonyl Group Make It Stereogenic Drug by Reductase Enzyme

Authors

  • Rezk R. Ayyad Pharmaceutical Medicinal Chemistry Department, Faculty of Pharmacy, Hilla University, Babylon, Iraq
  • Yasser Abdel Allem Hassan Pharmaceutics and Pharmaceutical Technology Department, Faculty of Pharmacy, Al-Kitab University, Kirkuk, Iraq
  • Ahmed G. El-Dahshan Ministry of Health, Arab Republic of Egypt
  • Mennah G. El-Dahshan Ministry of Health, Arab Republic of Egypt
  • Sherif G. El-Dahshan Ministry of Health, Arab Republic of Egypt
  • Ahmed R. Ayyad Faculty of Medicine, Asfendiyarov Kazakh National Medical University, Almaty, Kazakhstan

Keywords:

metabolism, reductase enzyme, carbonyl group, stereogenic drug, chiral carbon

Abstract

The metabolism is biotransformation refers to the processes by which the body chemically alters drugs, transforming them into different chemical compounds called metabolites. One of these processes is reduction of the drugs by reductase enzyme which add hydrogen to the compound, e.g. acetohexamide (oral hypoglycemic drug), loxoprofen (analgesic), haloperidol (antipsychotic drug), oxisuran (immunosuppressive agent), bupropion (antidepressant drug). All of these drugs contain a carbonyl group, which is reduced by reductase enzyme and converted into a chiral carbon, which makes the drug stereogenic.

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Published

2025-12-15

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Section

Articles