Source botanique

Dehydrocorydalin has anti-inflammatory,antinociceptive,antiplatelet,and anti-tumor effects and can protect the cardiovascular system. Dehydrocorydaline stimulates p38 MAPK activation, which can enhance heterodimerization of MyoD and E proteins, thus resulting in MyoD activation and myoblast differentiation. Dehydrocorydaline inhibits MCF-7 cell proliferation by inducing apoptosis mediated by regulating Bax/Bcl-2, activating caspases as well as cleaving PARP.

Salireposide is a phytochemical compound, specifically classified as a glucoside. It is derived from Salix species, commonly known as willows. This compound has been identified in the bark and other parts of these plants, where it occurs naturally. The mode of action of Salireposide involves its potential interaction with various biological pathways, possibly exerting anti-inflammatory and antioxidant effects. Its mechanism is thought to include modulation of signaling pathways related to oxidative stress and inflammation, though detailed molecular interactions are still the subject of ongoing research. Salireposide is utilized in scientific studies focusing on its therapeutic potential, particularly in the areas of anti-inflammatory and analgesic applications. Researchers explore its implications in managing conditions associated with oxidative stress and inflammation, contributing to the development of novel therapeutic agents derived from natural products. While its full pharmacological profile is not completely elucidated, Salireposide represents a promising candidate for further investigation in the field of natural product pharmacology.

Gypenoside XVII is a bioactive compound, which is a saponin derived from the plant Gynostemma pentaphyllum, commonly known as Jiaogulan. This compound is part of a broader category of plant-derived triterpenoid saponins that exhibit diverse biological activities. Gypenoside XVII functions primarily through its modulation of signaling pathways, including antioxidant, anti-inflammatory, and metabolic regulatory mechanisms. It affects key molecular targets and pathways, such as AMPK activation and nitric oxide production, offering potential therapeutic benefits. Gypenoside XVII is being studied for its potential applications in various health-related fields. Its antioxidant properties suggest a role in combating oxidative stress-related diseases, while its anti-inflammatory effects may be beneficial in conditions involving chronic inflammation. Moreover, its influence on lipid metabolism points to possible applications in metabolic disorders such as obesity and diabetes. Current research is exploring its therapeutic potential, underlying molecular mechanisms, and possible integration into more comprehensive treatment strategies. As a secondary metabolite from a plant traditionally used in herbal medicine, Gypenoside XVII continues to be an intriguing subject in the exploration of natural products for health improvement.

Notoginsenoside Fe can induce gap junction-mediated intercellular communication (GJIC) reductions; and gap junctions have been shown or are believed to be involved in the pathogenesis of many inherited and acquired human diseases, agents that regulate the GJIC function may facilitate prevention and treatment of GJIC-involved diseases.

Hesperidin, a bioflavonoid, is an abundant and inexpensive by-product of Citrus cultivation, has antioxidant, anti-inflammatory, hypolipidemic, vasoprotective and anticarcinogenic and cholesterol lowering actions; can improves the health of capillaries by reducing the capillary permeability; can inhibit following enzymes: phospholipase A2, lipoxygenase, HMG-CoA reductase and cyclo-oxygenase.

Kaempferide has a variety of effects including anti-carcinogenic, anti-inflammatory, anti-oxidant, anti-bacterial and anti-viral properties.it can protect DNA from radiation induced lesions resulting from radiation exposures under in vitro and ex vivo conditions.

Quercetin 3-O-(4''-O-acetyl)-α-L-rhamnopyranoside is a specialized flavonoid glycoside, which is a derivative of the flavonoid quercetin. It is primarily sourced from various plant species known for their high flavonoid content. The compound is characterized by its unique glycosylation pattern, where an acetyl group is esterified to the 4'' position of the rhamnose moiety. The mode of action of this compound involves its potential as an antioxidant, attributed to the quercetin core, which scavenges free radicals and reduces oxidative stress in biological systems. This activity is particularly concentrated in the cellular pathways where oxidative damage is mediated by reactive oxygen species. Quercetin 3-O-(4''-O-acetyl)-α-L-rhamnopyranoside is often utilized in research focused on natural antioxidants, with applications in pharmacology and biochemistry. It is investigated for its potential benefits in mitigating oxidative stress-related diseases, including cardiovascular ailments and neurodegenerative disorders. Its role as a bioactive compound makes it a subject of interest in exploring natural sources of antioxidants for therapeutic purposes.