shikimic

3,4-O-Isopropylidene-shikimic acid (3,4-O-Isopropylidene shikimic acid) exhibits significant anti-inflammatory, anti-thrombosis, antioxidant, and analgesic effects, and provides protective benefits against trinitrobenzenesulfonic acid-induced experimental colitis in rats, likely because of its antioxidant properties.

Shikimic Acid (Shikimate) is a tri-hydroxy cyclohexene carboxylic acid important in the biosynthesis of so many compounds that the shikimate pathway is named after it.

5-O-Caffeoylshikimic acid shows anti-oxidative activity; it also shows anti-inflammatory activity, the underlying mechanism was associated with downregulation of nuclear factor-κB.

3,5-Di-O-galloylshikimic acid is a useful organic compound for research related to life sciences. The catalog number is T123852 and the CAS number is 95753-52-9.

3,4-Di-o-galloylshikimicacid is a useful organic compound for research related to life sciences. The catalog number is T123853 and the CAS number is 95753-51-8.

3-O-Caffeoylshikimic acid (Compound 8) is a phenolic compound isolated from Livistona chinensis that exhibits antioxidant activity and inhibits the proliferation of multiple human cancer cell lines, including HepG2, HL-60, K562, and CNE-1, with IC50 values ranging from 5 to 150 μM, supporting its relevance in anticancer and oxidative stress research.

5-0-Galloylshikimicacid is a useful organic compound for research related to life sciences. The catalog number is T126409 and the CAS number is 110082-91-2.

4-O-Caffeoylshikimic acid is a natural product from Illicium verum.

(-)-3-Dehydroshikimic acid is a key intermediate in aromatic amino acid synthesis and exhibits antioxidant properties.

Ketomycin is an antibiotic agent. It is formed from shikimic acid via chorismic acid and prephenic acid.

Rhizocarpic acid is a derivative of shikimic acid.