| Weight | 174.152 g/mol |
|---|---|
| Formula | C7H10O5 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
shikimic acid (138-59-0)
Score:
#1004 in Biochemistry
,
#2642 in Biology
,
#3299 in Chemistry
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- Sigma-Aldrich - shikimic acid21.00 - 439.00 USD
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- Shikimic acid : metabolism and metabolites (1993)
- Metabolic engineering for microbial production of shikimic acid. (Metabolic Engineering, 2003)
- From glucose to aromatics: recent developments in natural products of the shikimic acid pathway (Tetrahedron, 1978)
- Tolerance and accumulation of shikimic acid in response to glyphosate applications in glyphosate-resistant and nonglyphosate-resistant cotton (Gossypium hirsutum L.). (Journal of Agricultural and Food Chemistry, 2002)
- SHIKIMIC ACID AND QUINIC ACID : REPLACING ISOLATION FROM PLANT SOURCES WITH RECOMBINANT MICROBIAL BIOCATALYSIS (Journal of the American Chemical Society, 1999)
- Phosphoenolpyruvate Availability and the Biosynthesis of Shikimic Acid (Biotechnology Progress, 2003)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C(C(C(C=C1C(=O)O)O)O)O
-
InChIKeyJXOHGGNKMLTUBP-UHFFFAOYSA-N
- Pubchem - shikimic acid
- Wikipedia - shikimic acid
Shikimic acid, more commonly known as its anionic form shikimate, is a cyclohexene, a cyclitol and a cyclohexanecarboxylic acid. It is an important biochemical metabolite in plants and microorganisms. Its name comes from the Japanese flower shikimi (, the Japanese star anise, Illicium anisatum), from which it was first isolated in 1885 by Johan Fredrik Eykman.
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shikimic acid
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