CAS 556-27-4
:Alliin
Description:
Alliin, with the CAS number 556-27-4, is a sulfur-containing compound primarily found in garlic (Allium sativum) and is responsible for many of its health benefits and characteristic aroma. It is a colorless, crystalline substance that is soluble in water and has a slightly bitter taste. Alliin is a derivative of the amino acid cysteine and is classified as a sulfoxide. When garlic is crushed or chopped, alliin is converted into allicin through the action of the enzyme alliinase, which is responsible for garlic's pungent smell and many of its therapeutic properties. Alliin itself is known for its potential health benefits, including antimicrobial, anti-inflammatory, and antioxidant effects. It is also studied for its role in cardiovascular health and its ability to enhance the immune system. Due to its instability, alliin is typically not found in significant amounts in processed garlic products, making fresh garlic a more potent source of this compound.
Formula:C6H11NO3S
InChI:InChI=1S/C6H11NO3S/c1-2-3-11(10)4-5(7)6(8)9/h2,5H,1,3-4,7H2,(H,8,9)/t5-,11-/m0/s1
InChI key:InChIKey=XUHLIQGRKRUKPH-DYEAUMGKSA-N
SMILES:S(C[C@@H](C(O)=O)N)(CC=C)=O
Synonyms:- (+)-<span class="text-smallcaps">L</span>-Alliin
- (S)-3-(Allylsulphinyl)-L-alanine
- 3-(Allylsulfinyl)alanin
- 3-(Prop-2-En-1-Ylsulfinyl)Alanine
- 3-(prop-2-en-1-ylsulfinyl)-L-alanine
- <span class="text-smallcaps">L</span>-Alanine, 3-(2-propenylsulfinyl)-, (S)-
- <span class="text-smallcaps">L</span>-Alanine, 3-[(S)-2-propenylsulfinyl]-
- <span class="text-smallcaps">L</span>-Cysteine, S-2-propen-1-yl-, S-oxide, [S(S)]-
- Alanine, 3-(allylsulfinyl)-
- Alanine, 3-(allylsulfinyl)-, (S)-<span class="text-smallcaps">L</span>-
- L-Alanine, 3-(2-propenylsulfinyl)-, (S)-
- S-Allyl-<span class="text-smallcaps">L</span>-cysteine-(+)-sulfoxide
- S-Allyl-L-Cysteinesulphoxide
- S-Allyl-L-cystein-S-oxid
- Alanine, 3-(allylsulfinyl)-, (S)-L-
- L-Alanine, 3-[(S)-2-propenylsulfinyl]-
- See more synonyms
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Found 9 products.
(+)-L-Alliin
CAS:(+)-L-Alliin analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C6H11NO3SPurity:(HPLC) ≥98%Color and Shape:PowderMolecular weight:177.23Alliin
CAS:<p>Other organo-sulfur acid compounds</p>Formula:C6H11NO3SColor and Shape:White Brown PowderMolecular weight:177.04596L-Alanine, 3-[(S)-2-propenylsulfinyl]-
CAS:Formula:C6H11NO3SPurity:97%Color and Shape:SolidMolecular weight:177.2214Alliin
CAS:<p>Alliin, a garlic-derived organosulfur, may combat inflammation in ALI by triggering PPARγ and blocking NF-κB.</p>Formula:C6H11NO3SPurity:99.39% - 99.62%Color and Shape:White To Off White Crystalline PowderMolecular weight:177.22L(+)-Alliin
CAS:<p>L(+)-Alliin is a naturally occurring organosulfur compound, which is a notable component derived from garlic (Allium sativum). It exists primarily in the intact garlic cloves and acts as a precursor to allicin, the compound responsible for garlic's characteristic aroma and many of its health benefits. When garlic is crushed or chopped, enzymatic reactions convert L(+)-Alliin to allicin through the action of the enzyme alliinase.</p>Formula:C6H11NO3SPurity:Min. 97 Area-%Color and Shape:White Off-White PowderMolecular weight:177.22 g/mol(+)-L-Alliin
CAS:Controlled Product<p>Applications (+)-L-Alliin is a precursor to Allicin (A543500), naturally formed by the action of the enzyme allicinase on alliin when the tissue of the garlic bulb is disrupted. Allicin shows antibacterial and antioxidant activity. Alliin shows cardiovascular protective properties as well.<br>References Yamada, Y., et al.: Antimicrob. Agents Chemother., 11, 743 (1977), Mayeux, P.R., et al.: Agents Actions, 25, 182 (1988), Freeman, F., et al.: J. Agric. Food Chem., 43, 2332 (1995), Macpherson, L.J., et al.: Curr. Biol., 15, 929 (2005); Yeh, Y. et al.: J. Nutr., 131, 989S (2001);<br></p>Formula:C6H11NO3SColor and Shape:NeatMolecular weight:177.22









