Chemistry:Corosolic acid

From HandWiki
Corosolic acid
Chemical structure of corosolic acid
Names
IUPAC name
2α,3β-Dihydroxyurs-12-en-28-oic acid
Systematic IUPAC name
(1S,2R,4aS,6aS,6bR,8aR,10R,11R,12aR,12bR,14bS)-10,11-Dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-octadecahydropicene-4a(2H)-carboxylic acid
Other names
Glucosol; Corsolic acid; Colosic acid; 2α-Hydroxyursolic acid
Identifiers
3D model (JSmol)
ChemSpider
UNII
Properties
C30H48O4
Molar mass 472.710 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Tracking categories (test):


Corosolic acid is a pentacyclic triterpene acid found in Lagerstroemia speciosa. It is similar in structure to ursolic acid, differing only in the fact that it has a 2-alpha-hydroxy attachment.[1]

ursolic acid

References

  1. Baba, Kosuke; Hiramatsu, Reiko; Suradej, Benjamart; Tanigaki, Riho; Koeda, Sayaka; Waku, Tomonori; Kataoka, Takao (2018). "Asiatic Acid, Corosolic Acid, and Maslinic Acid Interfere with Intracellular Trafficking and N-Linked Glycosylation of Intercellular Adhesion Molecule-1.". Biological and Pharmaceutical Bulletin 41 (12): 1757–1768. doi:10.1248/bpb.b18-00276. PMID 30504678.