Vinyldithiin
Vinyldithiins, more precisely named 3-vinyl-4H-1,2-dithiin and 2-vinyl-4H-1,3-dithiin, are organosulfur phytochemicals formed in the breakdown of allicin from crushed garlic (Allium sativum). Vinyldithiins are Diels-Alder dimers of thioacrolein, H2C=CHCH=S, formed in turn by decomposition of allicin.[1] In garlic supplements, vinyldithiins are only found in garlic oil macerates that are made by incubation of crushed garlic in oil.[2]
Structure and occurrence
When a garlic clove is crushed, the enzyme alliinase is released forming allicin from the cysteine sulfoxide alliin. Allicin breaks down into additional organosulfur compounds. In the presence of oil or organic solvents, among the compounds formed are the isomeric vinyldithiins and ajoene. As shown in the Scheme, allicin (1) decomposes into 2-propenesulfenic acid (2) and thioacrolein (3). Compound 2 reforms allicin while 3 gives Diels-Alder dimers 3-vinyl-4H-1,2-dithiin (4) and 2-vinyl-4H-1,3-dithiin (5).[1][3] Garlic cloves yield about 2.5-4.5 mg of allicin per gram when crushed. One fresh garlic clove weighs 2-4 g.[4]
Potential health benefits
 | This section needs more reliable medical references for verification or relies too heavily on primary sources. (February 2015) |  |
Vinyldithiins have been investigated as a preventative for cardiovascular disease and as antioxidants. In the early 1980s, it was noted that people in the Mediterranean had lower risk of cardiovascular disease.[5] Since garlic is used extensively in the Mediterranean, it is hypothesized that the chemicals in garlic might have cardiovascular effects. Studies have been done measuring the use of garlic for controlling serum cholesterol levels. Analysis of these studies show that vinyldithiins in garlic have little to no effect on serum lipids.[6] Vinyldithiins in garlic have been shown to significantly lower the incidence of platelet aggregation.[7] Reduction of platelet aggregation may result in reduction of myocardial infarction or ischemic stroke. Ingestion of foods containing vinyldithiins and other organosulfur compounds may decrease the risk of gastric and colon cancer.[8] 2-Vinyl-4H-1,2-dithiin was found to exhibit inhibitory activity against lipid hydroperoxide (LOOH) formation in human low-density lipoprotein (LDL).[9] A copolymer of 2-vinyl-4H-1,2-dithiin and N-vinylpyrrolidone has been patented as a biocompatible polymer with antithrombogenic (antithrombotic) and antibiotic properties.[10]
References
- ^ a b Block, E (2010). Garlic and Other Alliums: The Lore and the Science. Royal Society of Chemistry. ISBN 0-85404-190-7.
- ^ Lawson LD. Garlic: a review of its medicinal effects and indicated active compounds. In: Lawson LD, Bauer R, eds. Phytomedicines of Europe: Chemistry and Biological Activity. Washington, D. C.: American Chemical Society; 1998:177-209.
- ^ http://lpi.oregonstate.edu/infocenter/phytochemicals/garlic/
- ^ Lawson LD. Garlic: a review of its medicinal effects and indicated active compounds. In: Lawson LD, Bauer R, eds. Phytomedicines of Europe: Chemistry and Biological Activity. Washington, D. C.: American Chemical Society; 1998:177-209.
- ^ Keys A. Wine, garlic, and CHD in seven countries. Lancet. 1980;1(8160):145-146.
- ^ Gardner CD, Lawson LD, Block E, et al. Effect of raw garlic vs commercial garlic supplements on plasma lipid concentrations in adults with moderate hypercholesterolemia: a randomized clinical trial. Arch Intern Med. 2007;167(4):346-353.
- ^ Rahman K, Billington D. Dietary supplementation with aged garlic extract inhibits ADP-induced platelet aggregation in humans. J Nutr. 2000;130(11):2662-2665.
- ^ Fleischauer AT, Poole C, Arab L. Garlic consumption and cancer prevention: meta-analyses of colorectal and stomach cancers. Am J Clin Nutr. 2000;72(4):1047-1052.
- ^ Nishimura H, Higuchi O, Tateshita K. Antioxidative activity of sulfur-containing compounds in Allium species for human LDL oxidation in vitro. Biofactors 2004;21(1-4):277-280.
- ^ Hermes RE. Antithrombogenic and antibiotic composition and methods of preparation thereof. US 4917921, January 1, 1990. http://www.osti.gov/bridge/product.biblio.jsp?osti_id=867345