Global Information Lookup Global Information

Allixin information


Allixin
Names
Preferred IUPAC name
3-Hydroxy-5-methoxy-6-methyl-2-pentyl-4H-pyran-4-one
Identifiers
CAS Number
  • 125263-70-9 ☒N
3D model (JSmol)
  • Interactive image
ChemSpider
  • 77892 checkY
PubChem CID
  • 86374
UNII
  • 851A356OPF checkY
CompTox Dashboard (EPA)
  • DTXSID00154719 Edit this at Wikidata
InChI
  • InChI=1S/C12H18O4/c1-4-5-6-7-9-10(13)11(14)12(15-3)8(2)16-9/h13H,4-7H2,1-3H3 checkY
    Key: OHRPDNHRQKOLGN-UHFFFAOYSA-N checkY
  • InChI=1S/C12H18O4/c1-4-5-6-7-9-10(13)11(14)12(15-3)8(2)16-9/h13H,4-7H2,1-3H3
SMILES
  • O=C1C(/OC)=C(\O/C(=C1/O)CCCCC)C
Properties
Chemical formula
C12H18O4
Molar mass 226.272 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references

Allixin is a phytoalexin found in garlic (Allium sativum) bulbs. It was first isolated and characterized in 1989.[1] When garlic is stored for long periods of time, it can form visible accumulations of crystalline allixin on its surface, particularly in areas where tissue has become necrotic.[2] After 2 years of storage, the amount of allixin accumulated can approach 1% of the dry weight of the cloves. Since allixin has weak antimicrobial activity,[1] these high concentrations are thought to be produced by the garlic bulb to protect itself from further damage from microorganisms.

Since allixin is found in high concentrations in garlic, there has been scientific interest in determining if it is responsible for any of the known health benefits of garlic. As a result of ongoing research, a variety of biological activities have been attributed to allixin. Pharmaceutical drug discovery research based on derivatives of allixin has followed.[3]

  1. ^ a b Kodera, Yukihiro; Matsuura, Hiromichi; Yoshida, Susumu; Sumida, Toshihiko; Itakura, Yoichi; Fuwa, Toru; Nishino, Hoyoku (1989). "Allixin, a stress compound from garlic". Chemical & Pharmaceutical Bulletin. 37 (6): 1656–1658. doi:10.1248/cpb.37.1656.
  2. ^ Kodera, Y; Ayabe, M; Ogasawara, K; Yoshida, S; Hayashi, N; Ono, K (2002). "Allixin Accumulation with Long-term Storage of Garlic". Chemical & Pharmaceutical Bulletin. 50 (3): 405–7. doi:10.1248/cpb.50.405. PMID 11911208.
  3. ^ Hiromura, Makoto; Sakurai, Hiromu (2008). "Action mechanism of metallo-allixin complexes as antidiabetic agents". Pure and Applied Chemistry. 80 (12): 2727–2733. doi:10.1351/pac200880122727.

and 4 Related for: Allixin information

Request time (Page generated in 0.5889 seconds.)

Allixin

Last Update:

Allixin is a phytoalexin found in garlic (Allium sativum) bulbs. It was first isolated and characterized in 1989. When garlic is stored for long periods...

Word Count : 942

Phytoalexin

Last Update:

effects. Allixin showed an anti-tumor promoting effect in vivo, inhibiting skin tumor formation by TPA in DMBA initiated mice. Herein, allixin and/or its...

Word Count : 1762

Glossary of chemical formulae

Last Update:

thiamine nitrate C12H18N4O2 E1210 C12H18O propofol 2078-54-8 C12H18O4 Allixin or 1,6-Hexanediol diacrylate C12H19N3O7 D-Fructose-L-histidine 25020-13-7...

Word Count : 107

C12H18O4

Last Update:

C12H18O4 (molar mass: 226.27 g/mol, exact mass: 226.1205 u) may refer to: Allixin Dibutyl squarate 1,6-Hexanediol diacrylate This set index page lists chemical...

Word Count : 59

PDF Search Engine © AllGlobal.net