CAS 52645-97-3

(5beta,8alpha,9beta,10alpha)-17-hydroxykauran-18-oic acid

Description:

(5beta,8alpha,9beta,10alpha)-17-hydroxykauran-18-oic acid, with the CAS number 52645-97-3, is a naturally occurring compound classified as a kaurene-type diterpenoid. This substance is characterized by its complex polycyclic structure, which includes multiple chiral centers, contributing to its stereochemistry. It typically exhibits biological activity, often associated with plant-derived compounds, and may play a role in various physiological processes. The presence of a hydroxyl group and a carboxylic acid functional group in its structure suggests potential for hydrogen bonding and reactivity, which can influence its solubility and interaction with biological targets. This compound is of interest in pharmacology and natural product chemistry due to its potential therapeutic applications, including anti-inflammatory and anticancer properties. Its extraction and characterization from plant sources can provide insights into its biosynthesis and ecological roles. Further research may explore its mechanisms of action and potential uses in medicine or agriculture.

Formula: C₂₀H₃₂O₃

InChI: InChI=1/C20H32O3/c1-18-7-3-8-19(2,17(22)23)15(18)6-9-20-10-13(4-5-16(18)20)14(11-20)12-21/h13-16,21H,3-12H2,1-2H3,(H,22,23)/t13-,14-,15-,16-,18+,19+,20-/m0/s1

Synonyms:

• Kauran-18-oic acid, 17-hydroxy-, (4α,16α)-
• Siegeskaurolic acid

Siegeskaurolic acid

CAS: 52645-97-3

Siegeskaurolic acid reduces inflammation and pain by blocking iNOS and COX-2 in macrophages via NF-kappaB inactivation.

Formula: C₂₀H₃₂O₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 320.47

Ref: TM-TN5019

Siegeskaurolic acid

CAS: 52645-97-3

Siegeskaurolic acid is a naturally occurring triterpenoid compound, which is derived from various plant sources, such as those in the Burseraceae family. It is a pentacyclic triterpenoid that has garnered interest for its diverse biological activities. The mode of action of siegeskaurolic acid involves modulation of various biochemical pathways, including anti-inflammatory and antioxidant activities, primarily by interacting with cellular signaling molecules and enzymes.

Formula: C₂₀H₃₂O₃

Purity: Min. 95%

Molecular weight: 320.50 g/mol

Ref: 3D-CCA64597