Weight | 226.184 g/mol |
---|---|
Formula | C10H10O6 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 3 |
Aromatic Rings | 0 |
Rotatable Bonds | 4 |
chorismic acid (55508-12-8, 617-12-9)
Score:
#473 in Microbiology
,
#1648 in Biochemistry
,
#3725 in Biology
,
#4689 in Chemistry
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- Sigma-Aldrich - chorismic acid170.50 - 503.00 USD
- Fisher Scientific - Search for chorismic acid
- TCI - Search for chorismic acid
- THE BIOSYNTHESIS OF PHENYLALANINE AND TYROSINE; ENZYMES CONVERTING CHORISMIC ACID INTO PREPHENIC ACID AND THEIR RELATIONSHIPS TO PREPHENATE DEHYDRATASE AND PREPHENATE DEHYDROGENASE. (Biochimica et Biophysica Acta, 1965)
- Preliminary studies on the isolation and metabolism of an intermediate in aromatic biosynthesis: chorismic acid (Biochemical Journal, 1964)
- Chorismic acid: purification and some chemical and physical studies. (Biochemical Journal, 1964)
- On the mechanism of rearrangement of chorismic acid and related compounds (Journal of the American Chemical Society, 1987)
- Total synthesis of (-)-chorismic acid and (-)-shikimic acid (Journal of Organic Chemistry, 1987)
- Highly stereocontrolled synthesis of some polyfunctionalized cyclohexenes. A short formal total synthesis of ()-chorismic acid (Journal of Organic Chemistry, 1987)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC=C(C(=O)O)OC1C=C(C=CC1O)C(=O)O
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InChIKeyWTFXTQVDAKGDEY-UHFFFAOYSA-N
- Pubchem - chorismic acid
- Wikipedia - Chorismic acid
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, tryptophan, and tyrosine Indole, indole derivatives and tryptophan 2,3-Dihydroxybenzoic acid (DHB) used for enterobactin biosynthesis The plant hormone salicylic acid Many alkaloids and other aromatic metabolites. The folate precursor para-aminobenzoate (pABA) The biosynthesis of Vitamin K and folate in plants and microorganisms.
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