Alliin: Difference between revisions

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{{chembox
{{DISPLAYTITLE:Alliin}}
| Verifiedfields = changed
{{Infobox chemical
| verifiedrevid = 477317756
| name = Alliin
|  Name = Alliin
| image = Alliin.svg
|   ImageFile = Alliin Structural Formula V.1.svg
| image_size = 200px
<!-- | ImageSize = 250px -->
| image_alt = Structural formula of alliin
|   ImageName = Alliin skeletal view
| pin = 556-27-4
|   ImageFile1 = L-alliin-3D-balls.png
| IUPAC_name = (S)-2-Amino-3-[(S)-prop-2-enylsulfinyl]propanoic acid
<!-- | ImageSize1 = 250px  -->
| other_names = S-Allyl-L-cysteine sulfoxide
|  ImageName1 = Alliin ball view
| section1 =  
|   IUPACName = (2''R'')-2-amino-3-[(''S'')-prop-2-enylsulfinyl]propanoic acid
| section2 =  
|   OtherNames = 3-(2-Propenylsulfinyl)alanine<br />(''S'')-3-(2-Propenylsulfinyl)-<small>L</small>-alanine<br />3-((''S'')-Allylsulfinyl)-L-alanine<br />''S''-Allyl-<small>L</small>-cysteine sulfoxide
| section3 =  
| Section1 = {{Chembox Identifiers
|  SMILES = C=CCS(=O)CC(C(=O)O)N
|  ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 7850537
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| ChEMBL = 464166
| InChI = 1/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
| InChIKey = XUHLIQGRKRUKPH-DYEAUMGKBA
| SMILES1 = O=S(CC=C)C[C@@H](C(=O)O)N
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 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
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = XUHLIQGRKRUKPH-DYEAUMGKSA-N
| CASNo_Ref = {{cascite|changed|??}}
| CASNo = 556-27-4
  }}
| Section2 = {{Chembox Properties
|  Formula = C<sub>6</sub>H<sub>11</sub>NO<sub>3</sub>S
|  MolarMass = 177.22 g/mol
|  Appearance = White to off white crystalline powder
|  Solubility = Soluble
|  MeltingPt = {{convert|163|-|165|C|F}}
  }}
| Section7 = {{Chembox Hazards
|   ExternalMSDS = [http://www.mpbio.com/includes/msds/ansi/en/194125-en-ansi.pdf External MSDS]
|   NFPA-H = 1 | NFPA-F = 1 | NFPA-R = 0  }}
}}
}}


'''Alliin''' {{IPAc-en|ˈ|æ|l|i|.|ɪ|n}} is a [[sulfoxide]] that is a natural constituent of fresh [[garlic]].<ref>{{cite journal
==Introduction==
  | author = Iberl, B
'''Alliin''' is a naturally occurring [[sulfoxide]] that is found in the [[garlic]] plant, ''Allium sativum''. It is a derivative of the amino acid [[cysteine]] and is responsible for many of the health benefits associated with garlic. Alliin itself is odorless, but when garlic is crushed or chopped, the enzyme [[alliinase]] converts alliin into [[allicin]], which is responsible for the characteristic odor of garlic and many of its biological effects.
  | title = Quantitative Determination of Allicin and Alliin from Garlic by HPLC
  | journal = Planta Med
  | volume = 56
  | issue =3
  | pages = 320–326
  | year = 1990
  | doi = 10.1055/s-2006-960969
  | pmid = 17221429
  | display-authors = 1
  | last2 = Winkler
  | first2 = Georg
  | last3 = Müller
  | first3 = Bernd
  | last4 = Knobloch
  | first4 = Karl
}}</ref> It is a derivative of the [[amino acid]] [[cysteine]]. When fresh garlic is chopped or crushed, the enzyme [[alliinase]] converts alliin into [[allicin]], which is responsible for the aroma of fresh garlic. Garlic has been used since antiquity as a therapeutic remedy for certain conditions now associated with [[oxygen toxicity]], and, when this was investigated, garlic did indeed show strong [[antioxidant]] and [[hydroxyl]] [[free radical|radical]]-scavenging properties, it is presumed owing to the alliin contained within.<ref>{{cite journal
  | author = Kourounakis, PN; Rekka, EA
  | title = Effect on active oxygen species of alliin and Allium sativum (garlic) powder
  | journal = Res Commun Chem Pathol Pharmacol.
  | volume = 74
  | issue = 2
  | pages = 249–252
  |date=November 1991
  | pmid = 1667340
}}</ref>


Alliin has been found to affect immune responses in blood.<ref>{{cite journal
==Chemical Structure and Properties==
  | author = Salman, H
Alliin is classified as a sulfoxide, which is a type of [[organosulfur compound]]. Its chemical formula is C<sub>6</sub>H<sub>11</sub>NO<sub>3</sub>S, and it has a molecular weight of 177.22 g/mol. The IUPAC name for alliin is (S)-2-Amino-3-[(S)-prop-2-enylsulfinyl]propanoic acid. The molecule contains a chiral center, making it optically active.
  | title = Effect of a garlic derivative (alliin) on peripheral blood cell immune responses
  | journal = Int J Immunopharmacol.
  | volume = 21
  | issue = 9
  | pages = 589–597
  |date=September 1999
  | pmid = 10501628
  | doi = 10.1016/S0192-0561(99)00038-7
  | display-authors = 1
  | last2 = Bergman
  | first2 = M
  | last3 = Bessler
  | first3 = H
  | last4 = Punsky
  | first4 = I
  | last5 = Djaldetti
  | first5 = M
}}</ref>


== Alliin ==
==Biosynthesis==
Alliin is synthesized in garlic plants from the amino acid [[cysteine]]. The biosynthetic pathway involves the incorporation of a sulfoxide group into the cysteine molecule, resulting in the formation of alliin. This process occurs in the cytoplasm of garlic cells and is part of the plant's natural defense mechanism against pests and pathogens.


[[File:Alliin Structural Formula V.1.svg|Alliin Structural Formula]]
==Biological Activity==
While alliin itself is not biologically active, it serves as a precursor to [[allicin]], which has been shown to have a variety of health benefits. Allicin exhibits antimicrobial, antifungal, and antioxidant properties. It is also believed to have cardiovascular benefits, such as reducing blood pressure and cholesterol levels.


'''Alliin''' is a sulfoxide primarily found in fresh garlic, serving as one of its primary constituents. Structurally, it is derived from the amino acid cysteine. A distinguishing characteristic of alliin is its ability, when exposed to the enzyme alliinase following the crushing or chopping of garlic, to convert into allicin. This transformation is credited for bestowing fresh garlic with its characteristic aroma.
==Enzymatic Conversion==
The conversion of alliin to allicin is catalyzed by the enzyme [[alliinase]]. This enzyme is released when garlic is crushed or chopped, allowing it to come into contact with alliin. The reaction is rapid and results in the formation of allicin, which is responsible for the pungent aroma of fresh garlic.


== Historical Context ==
==Health Benefits==
Since ancient times, garlic has held a revered position in traditional medicine. Historically, it has been utilized as a remedy for ailments that modern science now associates with oxygen toxicity. Upon investigation, garlic's therapeutic properties were validated, displaying significant antioxidant and hydroxyl radical-scavenging abilities. It is hypothesized that these benefits may be largely attributed to the presence of alliin<ref>Augusti KT. (1996). Therapeutic values of onion (Allium cepa L.) and garlic (Allium sativum L.). Indian Journal of Experimental Biology. 34(7):634-40.</ref>.
Garlic, and by extension alliin, has been used in traditional medicine for centuries. The health benefits attributed to garlic include:


== Biochemical Significance ==
* '''Cardiovascular Health''': Consumption of garlic has been associated with reduced risk of cardiovascular diseases. This is thought to be due to the effects of allicin and other sulfur compounds in garlic that help lower blood pressure and cholesterol levels.
Alliin stands out not just for its therapeutic potential but also for its unique structural features. Remarkably, it was the first natural product identified to possess both carbon- and sulfur-centered stereochemistry<ref>Block E. (1985). The chemistry of garlic and onions. Scientific American. 252(3):114-9.</ref>.


=== Immune System Interactions ===
* '''Antimicrobial Effects''': Allicin, derived from alliin, has been shown to have broad-spectrum antimicrobial activity against bacteria, viruses, and fungi.
Recent studies have spotlighted alliin's ability to modulate immune responses in blood<ref>Chowdhury AK, Ahsan M, Islam SN, Ahmed ZU. (1991). Efficacy of aqueous extract of garlic & allicin in experimental shigellosis in rabbits. The Indian Journal of Medical Research. 93:33-6.</ref>. This discovery hints at a broader range of therapeutic applications and reinforces the need for further studies.


== Allicin: The Transformation Product ==
* '''Antioxidant Properties''': Garlic contains antioxidants that help protect cells from oxidative damage, which is linked to aging and various diseases.
As previously mentioned, when garlic is subjected to physical disruption, such as crushing or chopping, the enzyme alliinase acts on alliin, converting it to [[allicin]]. This compound, while being responsible for the aromatic nature of garlic, is also associated with a myriad of health benefits.


== Conclusion ==
==Conclusion==
Alliin's distinct properties, from its unique stereochemistry to its transformative abilities, make it an intriguing compound of study. Its therapeutic potentials, coupled with its rich historical background, underscore its significance in both culinary and medicinal domains.
Alliin is a key compound in garlic that, through enzymatic conversion to allicin, contributes to the health benefits associated with garlic consumption. Understanding the chemistry and biology of alliin and its derivatives is important for appreciating the medicinal properties of garlic.


== References ==
==References==
<references />
* Block, E. (2010). Garlic and Other Alliums: The Lore and the Science. Royal Society of Chemistry.
* Amagase, H., Petesch, B. L., Matsuura, H., Kasuga, S., & Itakura, Y. (2001). Intake of garlic and its bioactive components. ''The Journal of Nutrition'', 131(3), 955S-962S.
 
==See Also==
* [[Allicin]]
* [[Alliinase]]
* [[Garlic]]


[[Category:Sulfoxides]]
[[Category:Sulfoxides]]
[[Category:Sulfur amino acids]]
[[Category:Organosulfur compounds]]
[[Category:Nutrition]]{{food}} {{adapted}}
[[Category:Garlic]]
[[Category:Phytochemicals]]

Revision as of 02:11, 2 January 2025


Alliin
Alliin.svg
Identifiers
CAS Number
PubChem CID
ChemSpider ID
UNII
ChEBI
ChEMBL
Properties
Chemical Formula
Molar Mass
Appearance
Density
Melting Point
Boiling Point
Hazards
GHS Pictograms [[File:|50px]]
GHS Signal Word
GHS Hazard Statements
NFPA 704 [[File:|50px]]
References

Introduction

Alliin is a naturally occurring sulfoxide that is found in the garlic plant, Allium sativum. It is a derivative of the amino acid cysteine and is responsible for many of the health benefits associated with garlic. Alliin itself is odorless, but when garlic is crushed or chopped, the enzyme alliinase converts alliin into allicin, which is responsible for the characteristic odor of garlic and many of its biological effects.

Chemical Structure and Properties

Alliin is classified as a sulfoxide, which is a type of organosulfur compound. Its chemical formula is C6H11NO3S, and it has a molecular weight of 177.22 g/mol. The IUPAC name for alliin is (S)-2-Amino-3-[(S)-prop-2-enylsulfinyl]propanoic acid. The molecule contains a chiral center, making it optically active.

Biosynthesis

Alliin is synthesized in garlic plants from the amino acid cysteine. The biosynthetic pathway involves the incorporation of a sulfoxide group into the cysteine molecule, resulting in the formation of alliin. This process occurs in the cytoplasm of garlic cells and is part of the plant's natural defense mechanism against pests and pathogens.

Biological Activity

While alliin itself is not biologically active, it serves as a precursor to allicin, which has been shown to have a variety of health benefits. Allicin exhibits antimicrobial, antifungal, and antioxidant properties. It is also believed to have cardiovascular benefits, such as reducing blood pressure and cholesterol levels.

Enzymatic Conversion

The conversion of alliin to allicin is catalyzed by the enzyme alliinase. This enzyme is released when garlic is crushed or chopped, allowing it to come into contact with alliin. The reaction is rapid and results in the formation of allicin, which is responsible for the pungent aroma of fresh garlic.

Health Benefits

Garlic, and by extension alliin, has been used in traditional medicine for centuries. The health benefits attributed to garlic include:

  • Cardiovascular Health: Consumption of garlic has been associated with reduced risk of cardiovascular diseases. This is thought to be due to the effects of allicin and other sulfur compounds in garlic that help lower blood pressure and cholesterol levels.
  • Antimicrobial Effects: Allicin, derived from alliin, has been shown to have broad-spectrum antimicrobial activity against bacteria, viruses, and fungi.
  • Antioxidant Properties: Garlic contains antioxidants that help protect cells from oxidative damage, which is linked to aging and various diseases.

Conclusion

Alliin is a key compound in garlic that, through enzymatic conversion to allicin, contributes to the health benefits associated with garlic consumption. Understanding the chemistry and biology of alliin and its derivatives is important for appreciating the medicinal properties of garlic.

References

  • Block, E. (2010). Garlic and Other Alliums: The Lore and the Science. Royal Society of Chemistry.
  • Amagase, H., Petesch, B. L., Matsuura, H., Kasuga, S., & Itakura, Y. (2001). Intake of garlic and its bioactive components. The Journal of Nutrition, 131(3), 955S-962S.

See Also