| 3-o-Trans-p-coumaroyltormentic acid is a triterpenoid compound, which is typically isolated from various plant sources. These compounds are frequently found in traditional medicinal plants, where they contribute to the plants bioactive properties. The mode of action for 3-o-Trans-p-coumaroyltormentic acid involves the modulation of molecular pathways and interactions, which can lead to effects such as anti-inflammatory and antioxidant activities. This compound may inhibit specific enzymes or signaling pathways that contribute to cellular stress responses, making it a potential candidate for therapeutic applications. Recent studies explore its potential uses in pharmacology, particularly in the development of treatments for inflammatory disorders, oxidative stress-related diseases, and possibly in cancer therapy due to its ability to modulate cellular responses. Ongoing research aims to further elucidate its mechanisms and evaluate its efficacy in preclinical and clinical settings. As such, 3-o-Trans-p-coumaroyltormentic acid is a subject of considerable interest for researchers investigating natural compounds with health-modulating properties. Source: The leaves of Eriobotrya japonica calli Synonyms: (1R,2R,4aS,6aS,6bR,8aR,10R,11R,12aR,12bR,14bS)-1,11-dihydroxy-10-(((E)-3-(4-hydroxyphenyl)acryloyl)oxy)-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 CAS No: 121064-78-6 Molecular Formula: C39H54O7 Molecular Weight: 634.86 Appearance: White to off-white solid Purity: 98% Melting Point: 245C Solubility: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone Storage and Stability: May be stored at RT for short-term only. Long-term storage is recommended at -20C. Protected from air and light. For maximum recovery of product, centrifuge the original vial prior to removing the cap. |
