2922-42-1
2922-42-1
Chemical Structure
(-)-3-Dehydroshikimic acid
Synonym(s): 3-DHS; 5-Dehydroshikimic acid
- CAS No.: 2922-42-1
- Formula:C7H8O5
- Molecular Weight:172.14
IUPAC Name: (4S,5R)-4,5-dihydroxy-3-oxocyclohex-1-ene-1-carboxylic acid
InChIKey: SLWWJZMPHJJOPH-PHDIDXHHSA-N
SMILES: OC(C(C[C@H]([C@@H]1O)O)=CC1=O)=O
Biological Activity: (-)-3-Dehydroshikimic acid (3-DHS; 5-Dehydroshikimic acid) is an intermediate in the biosynthesis of aromatic amino acids. (-)-3-Dehydroshikimic acid shows antioxidant activity[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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(-)-3-Dehydroshikimic acid | 98.35% | (-)-3-Dehydroshikimic acid (3-DHS; 5-Dehydroshikimic acid) is an intermediate in the biosynthesis of aromatic amino acids. (-)-3-Dehydroshikimic acid shows antioxidant activity. | ||||||||||||||||||||
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(-)-3-Dehydroshikimic acid (Standard) | ≥98% | Isonicotinic acid (Standard) is the analytical standard of Isonicotinic acid. This product is intended for research and analytical applications. Isonicotinic acid is a metabolite of Isoniazid. Isoniazid is converted to Isonicotinic acid by hydrazinolysis, with the Isoniazid to Isonicotinic acid biotransformation also to be catalyzed by cytochrome P450 (CYP) enzymes, e.g., CYP2C. | ||||||||||||||||||||
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References
- [1]. Li K, et al. Microbial synthesis of 3-dehydroshikimic acid: a comparative analysis of D-xylose, L-arabinose, and D-glucose carbon sources. Biotechnol Prog. 1999 Sep-Oct;15(5):876-83. [Content Brief]
- [2]. Chang YC, et al. Antioxidant activity of 3-dehydroshikimic acid in liposomes, emulsions, and bulk oil. J Agric Food Chem. 2003 Apr 23;51(9):2753-7. [Content Brief]
