050-000-283 Shikimic Acid, CAS 138-59-0

SKU: 050-000-283 Category:
Get A Quote





  I would like to join the mailing list to receive updates from Stanford Chemicals.

Synonym (3R,4S,5R)-(−)-3,4,5-Trihydroxy-1-cyclohexenecarboxylic acid
Type Herb extract
Source Illicium verum Hook.f.
Key words aromatic biosynthetic pathway, anti-inflammation
Related products Glabridin, Pyrroloquinoline Quinone, Celastrol
Description

Description

Specifications of Shikimic Acid

Product Name Shikimic Acid
CAS Registry Number 138-59-0
Molecular Formula C7H10O5
Molecular Weight 174.15 g/mol
Purity 95%
Appearance White solid
Melting point 185°C
Shelf life 2 years
Functions Induces remyelination, anti-inflammation, relieve pain

Description of Shikimic Acid

Shikimic acid is a cyclohexenecarboxylic acid originally isolated from I. religiosum. It decreases lipid droplet accumulation in HepG2 cells and 3T3-L1 adipocytes when used at a concentration of 80 µM, as well as increases the levels of phosphorylated AMPK and decreases the levels of MID1IP1 in HepG2 and 3T3-L1 adipocytes when used at 40 µM.

shikimic acid

Applications of Shikimic Acid

Its naturally occurring form is a major biosynthetic precursor of phenylalanine, tyrosine, and tryptophan and hence of the majority of plant alkaloids. It is also involved in the biosynthesis of lignin, flavonoids and other important aromatic compounds. 

Reference:

  1. Bohm, B.A. Shikimic Acid (3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic Acid). Chem. Rev. 65(4), 435-466 (1965).
  2. Rawat, G., Tripathi, P., and Saxena, R.K. Expanding horizons of shikimic acid. Recent progresses in production and its endless frontiers in application and market trends. Appl. Microbiol. Biotechnol. 97(10), 4277-4287 (2013).
  3. Kim, M.J., Sim, D.Y., Lee, H.M., et al. Hypolipogenic effect of shikimic acid via inhibition of MID1IP1 and phosphorylation of AMPK/ACC. Int. J. Mol. Sci. 20(3), E582 (2019).
  4. Lu, F., Yin, D., Pu, Y., et al. Shikimic acid promotes oligodendrocyte precursor cell differentiation and accelerates remyelination in mice. Neurosci. Bull. 35(3), 434-446 (2019 ).