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Editorial

Special Issue “Structure–Activity Relationship of Natural Products”

Laboratory INSERM UMR 1097, Aix-Marseille University, 163, Parc Scientifique et Technologique de Luminy, Avenue de Luminy, Bâtiment TPR2, Case 939, 13288 Marseille, France
Molecules 2017, 22(5), 697; https://doi.org/10.3390/molecules22050697
Submission received: 25 April 2017 / Revised: 25 April 2017 / Accepted: 26 April 2017 / Published: 27 April 2017
(This article belongs to the Special Issue Structure-Activity Relationship of Natural Products)
This Special Issue of Molecules deals with the structure–activity relationship of natural compounds which possess some pharmacological/chemical properties of potential interest (from basic research to the clinical applications) in a wide range of areas, such as bacteriology, parasitology, cancerology, inflammation, etc.
The molecules that have been studied in the eleven published articles of the Special Issue are mainly derived from plants and are of a varied nature/complexity, ranging from glycyrrhizic acid to alkaloids. Echeverría, J. et al. [1] focus on the antibacterial properties of natural (plant-derived) flavones and flavanones. The potential of the natural flavonoid phloretin as an antimycobacterial agent (anti-tuberculosis), as well as an anti-inflammatory compound, was also investigated by Jeon and collaborators [2]. The capacity of the natural plant, pterostilbene, and its derivatives to act as anti-biofilm agents against Candida albicans was described by Hu et al. [3]. Finally, the antiparasitic (antiprotozoal) activity of triazole derivatives of dehydroabietic and oleanolic acids was reported by Pertino et al. [4]. Activities other than antimicrobial, such as anti-inflammatory activities, were further described by Li et al. [5] for plant diterpenoid alkaloids, and Nam et al. [6] for anthraquinone and its hydroxy derivatives, i.e. purpurin, anthrarufin and chrysazin (the latter also exhibiting antioxidative effects). The antioxidant properties of ferulates was investigated by Karamac et al. [7] whereas the free radical scavenging activity of soy isoflavone glycosides (Daidzin and Genistin)—and their 3’hydroxylated derivatives—was reported by Chiang et al. [8]. Such radical-scavenging activity, together with anti-tumor effects, were further described for Xanthoceras sorbifolia bunge/yellow horn plant polyphenols by Yang et al. [9]. Another interesting research article by Singh et al. [10] focused on the potential of glycyrrhizic acid to help both heart contractions and blood pressure. Finally, the last article of this Special Issue, by Liu et al. [11], dealt with the change in molecular content (organic acids, soluble sugars, anthocyanins, etc.) of the Chinese apple cultivar “Starkrimson” during the ripening period.
All these articles are actually highlighting the great potential of natural compounds—and their structural analogs—to act as candidate drugs to treat various diseases, including microbial infections. I would like to thank the authors for their outstanding work in the field of natural compounds.

References

  1. Echeverría, J.; Opazo, J.; Mendoza, L.; Urzúa, A.; Wilkens, M. Structure-Activity and Lipophilicity Relationships of Selected Antibacterial Natural Flavones and Flavanones of Chilean Flora. Molecules 2017, 22, 608. [Google Scholar] [CrossRef] [PubMed]
  2. Jeon, D.; Jeong, M.-C.; Jnawali, H.N.; Kwak, C.; Ryoo, S.; Jung, I.D.; Kim, Y. Phloretin Exerts Anti-Tuberculosis Activity and Suppresses Lung Inflammation. Molecules 2017, 22, 183. [Google Scholar] [CrossRef] [PubMed]
  3. Hu, D.-D.; Zhang, R.-L.; Zou, Y.; Zhong, H.; Zhang, E.-S.; Luo, X.; Wang, Y.; Jiang, Y.-Y. The Structure-Activity Relationship of Pterostilbene against Candida albicans Biofilms. Molecules 2017, 22, 360. [Google Scholar] [CrossRef] [PubMed]
  4. Pertino, M.W.; Vega, C.; Rolón, M.; Coronel, C.; Rojas de Arias, A.; Schmeda-Hirschmann, G. Antiprotozoal Activity of Triazole Derivatives of Dehydroabietic Acid and Oleanolic Acid. Molecules 2017, 22, 369. [Google Scholar] [CrossRef] [PubMed]
  5. Li, X.; Li, N.; Sui, Z.; Bi, K.; Li, Z. An Investigation on the Quantitative Structure-Activity Relationships of the Anti-Inflammatory Activity of Diterpenoid Alkaloids. Molecules 2017, 22, 363. [Google Scholar] [CrossRef] [PubMed]
  6. Nam, W.; Kim, S.P.; Nam, S.H.; Friedman, M. Structure-Antioxidative and Anti-Inflammatory Activity Relationships of Purpurin and Related Anthraquinones in Chemical and Cell Assays. Molecules 2017, 22, 265. [Google Scholar] [CrossRef] [PubMed]
  7. Karamać, M.; Koleva, L.; Kancheva, V.D.; Amarowicz, R. The Structure–Antioxidant Activity Relationship of Ferulates. Molecules 2017, 22, 527. [Google Scholar] [CrossRef] [PubMed]
  8. Chiang, C.-M.; Wang, D.-S.; Chang, T.-S. Improving Free Radical Scavenging Activity of Soy Isoflavone Glycosides Daidzin and Genistin by 3′-Hydroxylation Using Recombinant Escherichia coli. Molecules 2016, 21, 1723. [Google Scholar] [CrossRef] [PubMed]
  9. Yang, C.-Y.; Ha, W.; Lin, Y.; Jiang, K.; Yang, J.-L.; Shi, Y.-P. Polyphenols Isolated from Xanthoceras sorbifolia Husks and Their Anti-Tumor and Radical-Scavenging Activities. Molecules 2016, 21, 1694. [Google Scholar] [CrossRef] [PubMed]
  10. Singh, K.; Zaw, A.M.; Sekar, R.; Palak, A.; Allam, A.A.; Ajarem, J.; Chow, B.K.C. Glycyrrhizic Acid Reduces Heart Rate and Blood Pressure by a Dual Mechanism. Molecules 2016, 21, 1291. [Google Scholar] [CrossRef] [PubMed]
  11. Liu, Y.; Chen, N.; Ma, Z.; Che, F.; Mao, J.; Chen, B. The Changes in Color, Soluble Sugars, Organic Acids, Anthocyanins and Aroma Components in “Starkrimson” during the Ripening Period in China. Molecules 2016, 21, 812. [Google Scholar] [CrossRef] [PubMed]

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MDPI and ACS Style

Sabatier, J.-M. Special Issue “Structure–Activity Relationship of Natural Products”. Molecules 2017, 22, 697. https://doi.org/10.3390/molecules22050697

AMA Style

Sabatier J-M. Special Issue “Structure–Activity Relationship of Natural Products”. Molecules. 2017; 22(5):697. https://doi.org/10.3390/molecules22050697

Chicago/Turabian Style

Sabatier, Jean-Marc. 2017. "Special Issue “Structure–Activity Relationship of Natural Products”" Molecules 22, no. 5: 697. https://doi.org/10.3390/molecules22050697

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