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Peer-reviewedCC BY 4.0International Journal of Molecular Sciences

Structure–Activity Relationships of Natural and Synthetic Anthraquinones: Relevance for Pharmacology and Nutritional Supplementation

  1. 1Laboratory of Metabolomic and Proteomic Analysis, Federal Research Centre of Nutrition, Biotechnology and Food Safety, 109240 Moscow, Russia
  2. 2Department of Human Anatomy and Histology, Federal State Funded Educational Institution of Higher Education I.M. Sechenov First Moscow State Medical University, 119435 Moscow, Russia

Abstract

Anthraquinones constitute an extensive class of natural and synthetic derivatives. Natural anthraquinones are widely utilized as active ingredients in dietary supplements and traditional medicine. However, their inherent polypharmacology frequently complicates their biomedical application; while a broad spectrum of biological activities is advantageous in defined clinical settings, it often triggers off-target or adverse reactions under other conditions. Consequently, standardizing both chemical composition and biological efficacy remains a critical challenge for drug development and supplement formulation. Although extensive research has focused on the chemistry and pharmacology of anthraquinones, the underlying structure–activity relationships (SARs) remain fragmented across individual studies, lacking a unified framework that correlates substituent effects and electronic properties with specific biological endpoints. This review systematically evaluates the relationship between the chemical structure of anthraquinones and their biological properties. Specifically, we analyze how the pharmacological profiles and toxicity of anthraquinones are governed by three levels of structural modification: simple monomers, dimeric systems, and hybrid architectures, ultimately providing structure-guided principles for designing optimized therapeutics and safer dietary supplements.

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BibTeX
@article{yaglova2026structureactivity,
  title = {{Structure–Activity Relationships of Natural and Synthetic Anthraquinones: Relevance for Pharmacology and Nutritional Supplementation}},
  author = {Nataliya V. Yaglova and Sergey S. Obernikhin and Elina S. Tsomartova and Elizaveta V. Chereshneva and Dibakhan A. Tsomartova},
  journal = {International Journal of Molecular Sciences},
  year = {2026},
  month = oct,
  doi = {10.3390/ijms27208960},
  url = {https://www.mdpi.com/1422-0067/27/20/8960},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Structure–Activity Relationships of Natural and Synthetic Anthraquinones: Relevance for Pharmacology and Nutritional Supplementation
AU  - Nataliya V. Yaglova
AU  - Sergey S. Obernikhin
AU  - Elina S. Tsomartova
AU  - Elizaveta V. Chereshneva
AU  - Dibakhan A. Tsomartova
PY  - 2026
DA  - 2026/10/09
JO  - International Journal of Molecular Sciences
DO  - 10.3390/ijms27208960
UR  - https://www.mdpi.com/1422-0067/27/20/8960
AB  - Anthraquinones constitute an extensive class of natural and synthetic derivatives. Natural anthraquinones are widely utilized as active ingredients in dietary supplements and traditional medicine. However, their inherent polypharmacology frequently complicates their biomedical application; while a broad spectrum of biological activities is advantageous in defined clinical settings, it often triggers off-target or adverse reactions under other conditions. Consequently, standardizing both chemical composition and biological efficacy remains a critical challenge for drug development and supplement formulation. Although extensive research has focused on the chemistry and pharmacology of anthraquinones, the underlying structure–activity relationships (SARs) remain fragmented across individual studies, lacking a unified framework that correlates substituent effects and electronic properties with specific biological endpoints. This review systematically evaluates the relationship between the chemical structure of anthraquinones and their biological properties. Specifically, we analyze how the pharmacological profiles and toxicity of anthraquinones are governed by three levels of structural modification: simple monomers, dimeric systems, and hybrid architectures, ultimately providing structure-guided principles for designing optimized therapeutics and safer dietary supplements.
SN  - 1422-0067
ER  -