Advances in Phenazines over the Past Decade: Review of Their Pharmacological Activities, Mechanisms of Action, Biosynthetic Pathways and Synthetic Strategies
Autor: | Jiatong Cai, Hui-Ming Hua, Junjie Yan, Yiming Wang, Hao Cao, Dahong Li, Weiwei Liu |
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Rok vydání: | 2021 |
Předmět: |
Aquatic Organisms
Synthetic derivatives QH301-705.5 Antiparasitic medicine.drug_class Pharmaceutical Science Review Structure-Activity Relationship Bacterial Proteins Drug Discovery medicine Animals Biology (General) Pharmacology Toxicology and Pharmaceutics (miscellaneous) Chemistry phenazine Biological activity biosynthetic pathway Antimicrobial Biosynthetic Pathways Mechanism of action Biochemistry synthetic strategy Phenazines pharmacological activity medicine.symptom Large group mechanism of action |
Zdroj: | Marine Drugs, Vol 19, Iss 610, p 610 (2021) Marine Drugs |
ISSN: | 1660-3397 |
DOI: | 10.3390/md19110610 |
Popis: | Phenazines are a large group of nitrogen-containing heterocycles, providing diverse chemical structures and various biological activities. Natural phenazines are mainly isolated from marine and terrestrial microorganisms. So far, more than 100 different natural compounds and over 6000 synthetic derivatives have been found and investigated. Many phenazines show great pharmacological activity in various fields, such as antimicrobial, antiparasitic, neuroprotective, insecticidal, anti-inflammatory and anticancer activity. Researchers continued to investigate these compounds and hope to develop them as medicines. Cimmino et al. published a significant review about anticancer activity of phenazines, containing articles from 2000 to 2011. Here, we mainly summarize articles from 2012 to 2021. According to sources of compounds, phenazines were categorized into natural phenazines and synthetic phenazine derivatives in this review. Their pharmacological activities, mechanisms of action, biosynthetic pathways and synthetic strategies were summarized. These may provide guidance for the investigation on phenazines in the future. |
Databáze: | OpenAIRE |
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