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Synthesis, Antiviral, and Antibacterial Activity of the Glycyrrhizic Acid and Glycyrrhetinic Acid Derivatives.
Mohammed, E A H; Peng, Y; Wang, Z; Qiang, X; Zhao, Q.
  • Mohammed EAH; Institute of Medicinal Chemistry, School of Pharmacy of Lanzhou University, 730000 Lanzhou, China.
  • Peng Y; Institute of Medicinal Chemistry, School of Pharmacy of Lanzhou University, 730000 Lanzhou, China.
  • Wang Z; Institute of Medicinal Chemistry, School of Pharmacy of Lanzhou University, 730000 Lanzhou, China.
  • Qiang X; Institute of Medicinal Chemistry, School of Pharmacy of Lanzhou University, 730000 Lanzhou, China.
  • Zhao Q; Institute of Medicinal Chemistry, School of Pharmacy of Lanzhou University, 730000 Lanzhou, China.
Russ J Bioorg Chem ; 48(5): 906-918, 2022.
Article in English | MEDLINE | ID: covidwho-1965693
ABSTRACT
Glycyrrhizic acid and its primary metabolite glycyrrhetinic acid, are the main active ingredients in the licorice roots (glycyrrhiza species), which are widely used in several countries of the world, especially in east asian countries (China, Japan). These ingredients and their derivatives play an important role in treating many diseases, especially infectious diseases such as COVID-19 and hepatic infections. This review aims to summarize the different ways of synthesising the amide derivatives of glycyrrhizic acid and the main ways to synthesize the glycyrrhitinic acid derivatives. Also, to determine the main biological and pharmacological activity for these compounds from the previous studies to provide essential data to researchers for future studies. Supplementary Information The online version contains supplementary material available at 10.1134/S1068162022050132.
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Full text: Available Collection: International databases Database: MEDLINE Language: English Journal: Russ J Bioorg Chem Year: 2022 Document Type: Article Affiliation country: S1068162022050132

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Full text: Available Collection: International databases Database: MEDLINE Language: English Journal: Russ J Bioorg Chem Year: 2022 Document Type: Article Affiliation country: S1068162022050132