Chorismic acid
From Wikipedia, the free encyclopedia
| Chorismic acid | |
|---|---|
| IUPAC name | trans-3-([1-Carboxy- ethenyl]oxy)-4-hydroxy- 1,5-cyclohexadiene- 1-carboxylic acid |
| Identifiers | |
| CAS number | [617-12-9] |
| Properties | |
| Molecular formula | C10H10O6 |
| Molar mass | 226.18 g/mol |
| Melting point |
140 °C |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
|
Chorismic acid, more commonly known as its anionic form chorismate, is an important biochemical intermediate in plants and microorganisms. It is a precursor for:
- The aromatic amino acids phenylalanine and tyrosine
- Indole, indole derivatives and tryptophan
- 2,3-dihydroxybenzoic acid (DHB) used for enterobactin biosynthesis
- The plant hormone salicylic acid[1]
- Many alkaloids and other aromatic metabolites.
[edit] Biosynthesis
Shikimate → shikimate-3-phosphate → 5-enolpyruvylshikimate-3-phosphate → chorismate.

