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Hypoglycin A

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Hypoglycin
Hypoglycin
Names
IUPAC name
(S)-2-Amino-3-((S)-2-methylenecyclopropyl)propanoic acid
Other names
Hypoglycin A; Hypoglycine; 2-Methylenecyclopropanylalanine
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.189.936 Edit this at Wikidata
  • InChI=1S/C7H11NO2/c1-4-2-5(4)3-6(8)7(9)10/h5-6H,1-3,8H2,(H,9,10)/t5-,6+/m1/s1 checkY
    Key: OOJZCXFXPZGUBJ-RITPCOANSA-N checkY
  • InChI=1/C7H11NO2/c1-4-2-5(4)3-6(8)7(9)10/h5-6H,1-3,8H2,(H,9,10)/t5-,6+/m1/s1
    Key: OOJZCXFXPZGUBJ-RITPCOANBH
  • O=C(O)[C@@H](N)C[C@@H]1C(=C)C1
Properties
C7H11NO2
Molar mass 141.170 g·mol−1
Melting point 282 °C (540 °F; 555 K)
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 ?)

Hypoglycin A is a naturally-occurring amino acid derivative found in the unripened fruit of the Ackee tree (Blighia sapida). It is toxic if ingested, and is the causative agent of Jamaican vomiting sickness.[1]

Source

The entirety of the unripe Ackee fruit is toxic and contains large amounts of hypoglycin. The fruit is safe to eat only when the fruit is allowed to fully open and expose the large black seeds while on the tree. The levels of the toxin decrease over time though from approximately 1000 ppm to around 0.1 ppm in the mature fruit.[2]

Toxicity

Hypoglycin A is a type of Trojan Horse Inhibitor, also known as a Suicide Inhibitor, that in itself does not inhibit any biochemical pathway. However when mistaken for a branch chain amino acid, the toxicity arises from its metabolites. The branched-chain alpha-keto acid dehydrogenase complex, that would normally convert luecine, isoleucine, or valine into Acyl-CoA derivates, takes this hypoglycin A and metabolizes it into toxic inhibitors; methylene cyclopropyl acetic acid and methylenecyclopropane acetyl esters with carnitine and coenzyme A. The FAD prosthetic group necessary for the beta oxidation of fatty acids associates with the alpha carbon of MCPA-CoA creating an irreversible complex that inhibits the activity of acyl CoA dehydrogenase. In addition, MCPA-CoA blocks some enzymes that are required for gluconeogenesis.[2]

The reduction in gluconeogenesis and the reduction in fatty acid oxidation are thought to be the cause of most of the symptoms of Jamaican vomiting sickness. The blocking of fatty acid metabolism causes cells to start using glycogen for energy. Once glycogen is depleted, the body is unable to produce more, which leads to a severe case of hypoglycemia. These biochemical effects are detected by an excess of medium chain fatty acids in urine and acidosis. Key treatments are aimed at circumventing or counteracting the biochemical changes, and include IV fluids and glucose, and hemodialisis in the case of renal failure.[3]

Synthesis

In 1958, John Carbon, William Martin, and Leo Swett were the first to synthesize hypoglycin, in racemic form, starting from 2-bromopropene and ethyl diazoacetate to form the cyclopropane ring.[4]

An example of a synthesis pathway of hypoglycin A

See also

References

  1. ^ "Ackee Fruit Toxicity". Medscape.
  2. ^ a b "THE ACKEE FRUIT (BLIGHIA SAPIDA) AND ITS ASSOCIATED TOXIC EFFECTS". University of British Columbia.
  3. ^ "Hypoglycin". TOXNET.
  4. ^ Carbon, J. A.;Martin, W. B.;Swett, L. R. (1958), "SYNTHESIS OF α-AMINO- METHYLENECYCLOPROPANEPROPIONIC ACID (HYPOGLYCIN A)", J. Am. Chem. Soc., 80: 1002–1002, doi:10.1021/ja01537a066{{citation}}: CS1 maint: multiple names: authors list (link)
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