| Weight | 141.17 g/mol |
|---|---|
| Formula | C7H11NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
Hypoglycine (156-56-9)
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- Sigma-Aldrich - Search for Hypoglycine
- Fisher Scientific - Search for Hypoglycine
- TCI - Search for Hypoglycine
- Zur chemischen Kennzeichnung der Hypoglycine (Naturwissenschaften, 1956)
- Enantioselective synthesis of the methylenecyclopropane derivative related to hypoglycine, starting from malic acid (Tetrahedron Letters, 1991)
- PESTICIDE TOXICITY OR HYPOGLYCINE A POISONING (IVORY COAST, 1984)? (The Lancet, 1988)
- Process for the production of derivatives of hypoglycine a (1960)
- ChemInform Abstract: Enantioselective Synthesis of the Methylenecyclopropane Derivative Related to Hypoglycine, Starting from Malic Acid. (ChemInform, 2010)
- ChemInform Abstract: New Approach to Hypoglycine A Synthesis. (ChemInform, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC=C1CC1CC(C(=O)O)N
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InChIKeyOOJZCXFXPZGUBJ-UHFFFAOYSA-N
- Pubchem - Hypoglycine
- Wikipedia - hypoglycine a
Hypoglycin A is a naturally occurring amino acid derivative found in the unripened fruit of the Ackee tree (Blighia sapida) and in the seeds of the box elder tree (Acer negundo). It is toxic if ingested, and is the causative agent of Jamaican vomiting sickness. A 2017 Lancet report established a link between the consumption of unripened lychees (containing hypoglycin A or methylenecyclopropylglycine (MCPG)) resulting in hypoglycaemia and death from acute toxic encephalopathy.
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