CAS 539-86-6
:Allicin
Description:
Allicin is a sulfur-containing compound primarily known for its presence in garlic (Allium sativum) and is responsible for its distinctive aroma and many of its health benefits. It is formed when garlic is crushed or chopped, leading to the enzymatic conversion of alliin into allicin. Allicin is characterized by its potent antimicrobial properties, making it effective against a variety of bacteria, fungi, and viruses. It has also been studied for its potential cardiovascular benefits, including the ability to lower blood pressure and cholesterol levels. Chemically, allicin is unstable and can decompose into various sulfur compounds, which contributes to its short-lived nature in biological systems. Its structure features a thiosulfinate functional group, which is crucial for its biological activity. Allicin is often used in dietary supplements and natural remedies, although its efficacy can vary based on preparation and dosage. Overall, allicin is a fascinating compound with significant implications for health and nutrition, reflecting the broader benefits of garlic in traditional and modern medicine.
Formula:C6H10OS2
InChI:InChI=1S/C6H10OS2/c1-3-5-8-9(7)6-4-2/h3-4H,1-2,5-6H2
InChI key:InChIKey=JDLKFOPOAOFWQN-UHFFFAOYSA-N
SMILES:S(SCC=C)(CC=C)=O
Synonyms:- 2-Propene-1-sulfinic acid, thio-, S-allyl ester
- 2-Propene-1-sulfinothioic acid, S-2-propen-1-yl ester
- 2-Propene-1-sulfinothioic acid, S-2-propenyl ester
- 3-Prop-2-enylsulfinylsulfanylprop-1-ene
- 3-[(Prop-2-ene-1-sulfinyl)sulfanyl]prop-1-ene
- Alliin
- Allimed
- Alliosan
- Allisatin
- Allisure Liquid
- Allitrid
- Diallyl thiosulfinate
- Dianyctrsnlgide
- Garlic Extract
- S-Allyl acrylo-1-sulphinothioate
- S-prop-2-en-1-yl prop-2-ene-1-sulfinothioate
- Thio-2-propene-1-sulfinic acid S-allyl ester
- See more synonyms
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Found 11 products.
2-Propene-1-sulfinothioic acid, S-2-propenyl ester
CAS:Formula:C6H10OS2Purity:97%Color and Shape:LiquidMolecular weight:162.2730S-Allyl Prop-2-Ene-1-Sulfinothioate
CAS:S-Allyl Prop-2-Ene-1-SulfinothioatePurity:97% (isomers mixture)Molecular weight:162.27g/molAllicin
CAS:<p>Allicin exerts antioxidant, bactericidal, anti-cancer, anti-inflammatory activities, it exerts an inhibitory immunomodulatory effect on intestinal epithelial</p>Formula:C6H10OS2Purity:≥98%Color and Shape:Clear To Slightly Yellow LiquidMolecular weight:162.27Allicin - Mixture of mainly diallyldisulfide and diallyl trisulfide
CAS:<p>Allicin is a biologically active compound, primarily a mixture of diallyl disulfide and diallyl trisulfide, which is an organosulfur compound found predominantly in crushed garlic (Allium sativum). It originates from the enzymatic conversion of alliin through the action of alliinase when garlic is damaged or crushed. The mode of action of Allicin involves its ability to interact with and inhibit thiol-containing enzymes within microbial cells, which disrupts essential cellular processes and contributes to its potent antimicrobial properties. Additionally, Allicin exhibits a broad spectrum of activity against a variety of bacteria, viruses, and fungi.</p>Formula:C6H10OS2Purity:Min. 98%Color and Shape:Yellow PowderMolecular weight:162.28 g/molAllicin kit
CAS:<p>Kit for preparing fresh allicin from the alliin/allinase. This compound is very unstable with the typical odor of garlic from well known unpleasant sulfurpus degradation compounds. The stability of allicin is about 72 h under -20°C in a dark and oxygene free storage. The allicin kit is a method for preparing freshly allicin from the stable preproduct alliin with the natural enzyme alliinase from garlic.</p>Formula:C6H10OS2Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:162.28 g/molAllicin
CAS:<p>Allicin is an organosulfur compound, which is derived from garlic (Allium sativum) through the enzymatic conversion when garlic is crushed or chopped. The enzyme alliinase is activated, converting alliin into allicin, a biologically active molecule. This process represents a defense mechanism of the plant, as allicin is potent against various pathogens.</p>Formula:C6H10OS2Purity:Min. 95%Molecular weight:162.28 g/mol







