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
. 2015:2015:816364.
doi: 10.1155/2015/816364. Epub 2015 May 27.

A Review on Pharmacological Properties of Zingerone (4-(4-Hydroxy-3-methoxyphenyl)-2-butanone)

Affiliations
Review

A Review on Pharmacological Properties of Zingerone (4-(4-Hydroxy-3-methoxyphenyl)-2-butanone)

Bilal Ahmad et al. ScientificWorldJournal. 2015.

Abstract

Humans have been using natural products for medicinal use for ages. Natural products of therapeutic importance are compounds derived from plants, animals, or any microorganism. Ginger is also one of the most commonly used condiments and a natural drug in vogue. It is a traditional medicine, having some active ingredients used for the treatment of numerous diseases. During recent research on ginger, various ingredients like zingerone, shogaol, and paradol have been obtained from it. Zingerone (4-(4-hydroxy-3-methoxyphenyl)-2-butanone) is a nontoxic and inexpensive compound with varied pharmacological activities. It is the least pungent component of Zingiber officinale. Zingerone is absent in fresh ginger but cooking or heating transforms gingerol to zingerone. Zingerone closely related to vanillin from vanilla and eugenol from clove. Zingerone has potent anti-inflammatory, antidiabetic, antilipolytic, antidiarrhoeic, antispasmodic, and so forth properties. Besides, it displays the property of enhancing growth and immune stimulation. It behaves as appetite stimulant, anxiolytic, antithrombotic, radiation protective, and antimicrobial. Also, it inhibits the reactive nitrogen species which are important in causing Alzheimer's disease and many other disorders. This review is written to shed light on the various pharmacological properties of zingerone and its role in alleviating numerous human and animal diseases.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Chemical structure of zingerone. IUPAC name: [4-(3-methoxy-4-hydroxyphenyl)-butan-2-one].
Figure 2
Figure 2
Pharmacological dimensions of zingerone.

References

    1. Park E. J., Pezzuto J. M. Botanicals in cancer chemoprevention. Cancer and Metastasis Reviews. 2002;21(3-4):231–255. doi: 10.1023/A:1021254725842. - DOI - PubMed
    1. Zhang Y.-X., Li J.-S., Chen L.-H., Peng W.-W., Cai B.-C. Simultaneous determination of five gingerols in raw and processed ginger by HPLC. Chinese Pharmaceutical Journal. 2012;47(6):471–474.
    1. Cotton W. J. Production of zingerone. Google Patents, 1945.
    1. Takizawa M., Sato M., Kusuoku H., Sakasai M. Lipolysis stimulator. Google Patents, 2012.
    1. Rajan I., Narayanan N., Rabindran R., Jayasree P. R., Manish Kumar P. R. Zingerone protects against stannous chloride-induced and hydrogen peroxide-induced oxidative DNA damage in vitro. Biological Trace Element Research. 2013;155(3):455–459. doi: 10.1007/s12011-013-9801-x. - DOI - PubMed

MeSH terms