Limonin

Limonin
Ball-and-stick model of limonin
Names
IUPAC name
7,16-Dioxo-7,16-dideoxylimondiol
Other names
limonoate D-ring-lactone,
limonoic acid di-delta-lactone
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.236.039
Properties
C26H30O8
Molar mass 470.52 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Limonin is a limonoid, and a bitter, white, crystalline substance found in citrus and other plants. It is also known as limonoate D-ring-lactone and limonoic acid di-delta-lactone. Chemically, it is a member of the class of compounds known as furanolactones.

Sources

Limonin is enriched in citrus fruits and is often found at higher concentrations in seeds, for example orange and lemon seeds. Limonin is present in plants such as those of the Dictamnus genus.[1]

Presence in citrus products

Limonin and other limonoid compounds contribute to the bitter taste of some citrus food products. Researchers have proposed removal of limonoids from orange juice and other products (known as "debittering") through the use of polymeric films.[2]

Bioactivity and research

Ongoing research programs are examining the effects of limonin in human diseases. Citrus seed extracts reportedly have antiviral properties, inhibiting replication of retroviruses like HIV-1 and HTLV-I.[3] Neuroprotective effects of limonin have also been described.[1] Limonin reduces proliferation of colon cancer cells[4] and has been tested as an anti-obesity agent in mice.[5]

References

  1. 1 2 Yoon, J. S.; Yang, H.; Kim, S. H.; Sung, S. H.; Kim, Y. C. (2010). "Limonoids from Dictamnus dasycarpus Protect Against Glutamate-induced Toxicity in Primary Cultured Rat Cortical Cells". Journal of Molecular Neuroscience. 42 (1): 9–16. PMID 20155333. doi:10.1007/s12031-010-9333-1.
  2. ↑ Fayoux, S. P. C.; Hernandez, R. J.; Holland, R. V. (2007). "The Debittering of Navel Orange Juice Using Polymeric Films". Journal of Food Science. 72 (4): E143–E154. PMID 17995766. doi:10.1111/j.1750-3841.2007.00283.x.
  3. ↑ Balestrieri, E.; Pizzimenti, F.; Ferlazzo, A.; Giofrè, S. V.; Iannazzo, D.; Piperno, A.; Romeo, R.; Chiacchio, M. A.; Mastino, A.; MacChi, B. (2011). "Antiviral activity of seed extract from Citrus bergamia towards human retroviruses". Bioorganic & Medicinal Chemistry. 19 (6): 2084–2089. PMID 21334901. doi:10.1016/j.bmc.2011.01.024.
  4. ↑ Chidambara Murthy, K. N.; Jayaprakasha, G. K.; Kumar, V.; Rathore, K. S.; Patil, B. S. (2011). "Citrus Limonin and Its Glucoside Inhibit Colon Adenocarcinoma Cell Proliferation through Apoptosis". Journal of Agricultural and Food Chemistry. 59 (6): 2314–2323. PMID 21338095. doi:10.1021/jf104498p.
  5. ↑ Ono, E.; Inoue, J.; Hashidume, T.; Shimizu, M.; Sato, R. (2011). "Anti-obesity and anti-hyperglycemic effects of the dietary citrus limonoid nomilin in mice fed a high-fat diet". Biochemical and Biophysical Research Communications. 410 (3): 677–681. PMID 21693102. doi:10.1016/j.bbrc.2011.06.055.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.