Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Mar 24;19(3):3570-95.
doi: 10.3390/molecules19033570.

Structure-activity association of flavonoids in lung diseases

Affiliations
Review

Structure-activity association of flavonoids in lung diseases

João Henrique G Lago et al. Molecules. .

Abstract

Flavonoids are polyphenolic compounds classified into flavonols, flavones, flavanones, isoflavones, catechins, anthocyanidins, and chalcones according to their chemical structures. They are abundantly found in Nature and over 8,000 flavonoids have from different sources, mainly plant materials, have been described. Recently reports have shown the valuable effects of flavonoids as antiviral, anti-allergic, antiplatelet, antitumor, antioxidant, and anti-inflammatory agents and interest in these compounds has been increasing since they can be helpful to human health. Several mechanisms of action are involved in the biological properties of flavonoids such as free radical scavenging, transition metal ion chelation, activation of survival genes and signaling pathways, regulation of mitochondrial function and modulation of inflammatory responses. The anti-inflammatory effects of flavonoids have been described in a number of studies in the literature, but not frequently associated to respiratory disease. Thus, this review aims to discuss the effects of different flavonoids in the control of lung inflammation in some disorders such as asthma, lung emphysema and acute respiratory distress syndrome and the possible mechanisms of action, as well as establish some structure-activity relationships between this biological potential and chemical profile of these compounds.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Classification of flavonoids based on their chemical structure.
Figure 2
Figure 2
Chemical structures of flavonoids 150.
Figure 3
Figure 3
Inflammatory response and cells involved in inflammatory cascade. * shows the steps that provide evidence that flavonoids can act to counteract the inflammatory response.
Figure 4
Figure 4
Structure of quercetin as example of important requisites (unsaturation in the C ring, number and position of hydroxyl groups at ring B, carbonyl group at C-4 and non-glycosylation) for anti-inflammatory activity of flavonoids.

References

    1. Bravo L. Polyphenols: Chemistry, dietary sources, metabolism, and nutritional significance. Nutr. Rev. 1998;56:317–333. doi: 10.1111/j.1753-4887.1998.tb01670.x. - DOI - PubMed
    1. Caltagirone S., Ranelletti F.O., Rinelli A., Maggiano N., Colasante A., Musiani P., Aiello F.B., Piantelli M. Interaction with type II estrogen binding sites and antiproliferative activity of tamoxifen and quercetin in human non-small-cell lung cancer. Am. J. Respir. Cell Mol. Biol. 1997;17:51–59. doi: 10.1165/ajrcmb.17.1.2728. - DOI - PubMed
    1. Ranelletti F.O., Ricci R., Larocca L.M., Maggiano N., Capelli A., Scambia G., Benedetti-Panici P., Mancuso S., Rumi C., Piantelli M. Growth-inhibitory effect of quercetin and presence of type-II estrogen-binding sites in human colon-cancer cell lines and primary colorectal tumors. Int. J. Cancer. 1992;50:486–492. doi: 10.1002/ijc.2910500326. - DOI - PubMed
    1. Yoshida M., Sakai T., Hosokawa N., Marui N., Matsumoto K., Fujioka A., Nishino H., Aoike A. The effect of quercetin on cell cycle progression and growth of human gastric cancer cells. FEBS Lett. 1990;260:10–13. doi: 10.1016/0014-5793(90)80053-L. - DOI - PubMed
    1. Lee K.H., Yoo C.G. Simultaneous inactivation of GSK-3beta suppresses quercetin-induced apoptosis by inhibiting the JNK pathway. Am. J. Physiol. Lung Cell Mol. Physiol. 2013;304:L782–L789. doi: 10.1152/ajplung.00348.2012. - DOI - PubMed

Publication types

MeSH terms

LinkOut - more resources