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- Vinyldithiin abstract "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. In garlic supplements, vinyldithiins are only found in garlic oil macerates that are made by incubation of crushed garlic in oil.".
- Vinyldithiin thumbnail Formation_of_vinyldithiins_from_allicin.png?width=300.
- Vinyldithiin wikiPageID "31922947".
- Vinyldithiin wikiPageRevisionID "555367944".
- Vinyldithiin hasPhotoCollection Vinyldithiin.
- Vinyldithiin subject Category:Alkenes.
- Vinyldithiin subject Category:Allioideae.
- Vinyldithiin subject Category:Allium.
- Vinyldithiin subject Category:Anti-inflammatory_agents.
- Vinyldithiin subject Category:Antibiotics.
- Vinyldithiin subject Category:Antifungals.
- Vinyldithiin subject Category:Articles_created_via_the_Article_Wizard.
- Vinyldithiin subject Category:Dietary_antioxidants.
- Vinyldithiin subject Category:Garlic.
- Vinyldithiin subject Category:Phytochemicals.
- Vinyldithiin subject Category:Pungent_flavors.
- Vinyldithiin subject Category:Sulfoxides.
- Vinyldithiin subject Category:Thiosulfinates.
- Vinyldithiin type Agent109190918.
- Vinyldithiin type Agent114778436.
- Vinyldithiin type Anti-inflammatoryAgents.
- Vinyldithiin type Antibacterial102716205.
- Vinyldithiin type Antibiotic102716866.
- Vinyldithiin type Antibiotics.
- Vinyldithiin type Antifungal102720201.
- Vinyldithiin type Antifungals.
- Vinyldithiin type Antioxidant114724645.
- Vinyldithiin type CausalAgent100007347.
- Vinyldithiin type DietaryAntioxidants.
- Vinyldithiin type Drug103247620.
- Vinyldithiin type Inhibitor114724436.
- Vinyldithiin type Matter100020827.
- Vinyldithiin type Medicine103740161.
- Vinyldithiin type PhysicalEntity100001930.
- Vinyldithiin type Substance100020090.
- Vinyldithiin comment "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. In garlic supplements, vinyldithiins are only found in garlic oil macerates that are made by incubation of crushed garlic in oil.".
- Vinyldithiin label "Vinyldithiin".
- Vinyldithiin label "ビニルジチイン".
- Vinyldithiin sameAs ビニルジチイン.
- Vinyldithiin sameAs m.0gvvv22.
- Vinyldithiin sameAs Q11330876.
- Vinyldithiin sameAs Q11330876.
- Vinyldithiin sameAs Vinyldithiin.
- Vinyldithiin wasDerivedFrom Vinyldithiin?oldid=555367944.
- Vinyldithiin depiction Formation_of_vinyldithiins_from_allicin.png.
- Vinyldithiin isPrimaryTopicOf Vinyldithiin.