Gymnemic acid

Gymnemic acids are a class of chemical compounds isolated from the leaves of Gymnema sylvestre (Asclepiadaceae). They are anti-sweet compounds, or sweetness inhibitors.[1] After chewing the leaves, solutions sweetened with sugar taste like water.

Chemically, gymnemic acids are triterpenoid glycosides. The central structure is the aglycone gymnemagenin (C30H50O6).[2] This is adorned with a sugar such as glucuronic acid and with various ester groups. These variations give rise to the different gymnemic acids.[3] More than 20 homologs of gymnemic acid are known.[4]

Gymnemic acid I has the highest anti-sweet properties. It suppresses the sweetness of most of the sweeteners including intense artificial sweeteners such as aspartame and natural sweeteners such as thaumatin, a sweet protein. The anti-sweet activity is reversible, but sweetness recovery on the tongue can take more than 10 minutes.[5]

Example chemical structures
Gymnemic acids[5]
Chemical structure
NameGymnemic acid IGymnemic acid IIGymnemic acid IIIGymnemic acid IV
R1tigloyl2-methylbutanoyl2-methylbutanoyltigloyl
R2acetylacetylHH
CAS Number122168-40-5122144-48-3122074-65-1121903-96-6
PubChem ID11953919916178721426406614264063
Chemical formulaC43H66O14C43H68O14C41H66O13C41H64O13
Molar mass (g/mol)806.98809.00766.97764.95
gollark: I think trying to restrict this information from spreading around is... about as effective as DRM, really, for the reason that you can kind of control who gets information but not how it's used or spread out after they do.
gollark: Bots running on a user account instead of a bot one.
gollark: Not technically, they are explicitly.
gollark: Me hacking Discord.
gollark: No, it's just selfbots.

See also

Other anti-sweeteners:

  • Hodulcine, a dammarane-type triterpene glycoside from the leaves of Hovenia dulcis
  • Lactisole, sodium 2-(4-methoxyphenoxy)propanoate
  • Ziziphin, a triterpene glycoside, C51H80O18

References
  1. Stoecklin, Walter (1969). "Chemistry and physiological properties of gymnemic acid, the antisaccharine principle of the leaves of Gymnema sylvestre". Journal of Agricultural and Food Chemistry. 17 (4): 704. doi:10.1021/jf60164a011.
  2. CID 10051937 from PubChem
  3. Sheng, Huaming; Sun, Hongbin (2011). "Synthesis, biology and clinical significance of pentacyclic triterpenes: A multi-target approach to prevention and treatment of metabolic and vascular diseases". Natural Product Reports. 28 (3): 543. doi:10.1039/C0NP00059K. PMID 21290067.
  4. AD kinghorn and CM Compadre (1991). L O'Brien Nabors (ed.). Less common high-potency sweeteners. Alternative Sweeteners (2nd ed.). New York: Marcel Dekker. ISBN 0-8247-8475-8.
  5. Kurihara, Yoshie (1992). "Characteristics of antisweet substances, sweet proteins, and sweetness‐inducing proteins". Critical Reviews in Food Science and Nutrition. 32 (3): 231–52. doi:10.1080/10408399209527598. PMID 1418601.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.