Flavonoids

Pinocembroside analytical standard provided with w/w absolute assay, to be used for quantitative titration.

Glyasperin D is a flavonoid compound extracted from the root of Glycyrrhiza uralensis, which has potential antimicrobial activity against Helicobacter pylori.

Fustin analytical standard provided with w/w absolute assay, to be used for quantitative titration.

5,3'-Dihydroxyflavone is a flavonoid compound, which is a class of polyphenolic molecules. It is derived from various plants, where it occurs naturally as part of the complex biochemical repertoire involved in defense mechanisms and signaling processes. This compound acts as an antioxidant, neutralizing free radicals and reducing oxidative stress. It also exhibits potential neuroprotective effects by modulating specific signaling pathways and interacting with enzymes linked to inflammation and cellular health. The uses and applications of 5,3'-Dihydroxyflavone are explored in various scientific fields, particularly in pharmacology and biochemistry. Researchers are investigating its potential as a therapeutic agent for conditions such as neurodegenerative diseases, given its antioxidant properties and ability to influence neuronal survival pathways. Additionally, its anti-inflammatory effects make it a candidate for further study concerning chronic inflammatory conditions. Ongoing research is crucial to fully understand its mechanisms and therapeutic potential.

Neoschaftoside is a naturally occurring bioactive compound, which is an acylated flavonoid C-glycoside. It is primarily sourced from various plant species, including members of the Poaceae and Fabaceae families. The compound functions through its antioxidant and anti-inflammatory properties, interacting with cellular pathways to mitigate oxidative stress and modulate immune responses. These actions make neoschaftoside a compound of interest in pharmacological research, particularly in the study of chronic diseases where inflammation and oxidative damage are key pathological features. Its applications extend to potential therapeutic development in areas such as cardiovascular health, neuroprotection, and metabolic disorders. The ongoing investigation into its modes of action and bioavailability continues to reveal insights into its efficacy and potential as a natural therapeutic agent.

(rac)-Poriol (5,7,4'-Trihydroxy-6-methylflavanone) demonstrates antioxidant properties by effectively scavenging the free radical DPPH, with an IC50 value of 0.18 µg/mL. It can significantly inhibit LPS-induced NO production in RAW264.7 cells, achieving a 98.35% inhibition rate at a concentration of 10 μM, indicating its anti-inflammatory potential. Furthermore, (rac)-Poriol shows strong binding affinity with iNOS, COX-1, COX-2, TNF-α, and IL-1β.

Eupatorin - 98% is a high-purity flavonoid compound, which is extracted primarily from various plant species such as Eupatorium. This compound is renowned for its bioactive properties, engaging in numerous biochemical interactions that contribute to its therapeutic potentials. Eupatorin operates through multiple biochemical pathways as an inhibitor of specific enzymes like cytochrome P450s and as a modulator of cellular signaling pathways. This enables it to exert anti-inflammatory, anticancer, and antioxidant effects, making it a valuable subject of study in pharmaceutical and clinical research. The wide array of applications of Eupatorin - 98% includes studies focused on its anticancer potential. It has been observed to induce apoptosis in cancerous cells and inhibit tumor growth, making it a promising candidate for cancer therapy. Additionally, its anti-inflammatory and antioxidant properties render it useful in research aimed at treating chronic inflammatory diseases and neurodegenerative disorders. Eupatorin's role in these areas is an active field of research, with ongoing studies examining its molecular mechanisms and potential therapeutic applications.

(+)-Dihydrokaempferol analytical standard provided with w/w absolute assay, to be used for quantitative titration.

Carthamidin tetramethyl ether is a chemical compound classified as a flavonoid, which is a naturally occurring phytochemical. It is derived from the safflower plant (Carthamus tinctorius), which belongs to the Asteraceae family. The primary mode of action of Carthamidin tetramethyl ether involves its antioxidant properties, which allow it to scavenge free radicals and reduce oxidative stress. Additionally, it may interact with specific cellular pathways, influencing gene expression and enzyme activities related to inflammatory responses and cellular metabolism. Carthamidin tetramethyl ether is primarily studied for its potential applications in the fields of pharmacology and nutritional science. Researchers investigate its role as an antioxidant and anti-inflammatory agent, exploring its potential uses in preventing or treating conditions related to oxidative stress, such as cardiovascular diseases and inflammatory disorders. This compound is also of interest in the development of functional foods and nutraceuticals, where its natural origin and bioactivity offer promising avenues for enhancing health and wellness. As research progresses, its precise mechanisms and broader applications continue to be elucidated.

Oroxin A (Baicalein 7-O-glucoside) has antitussive and expectorant effects.

3-Hydroxyflavone analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.

Natural glycoside

Natural glycoside

Didymin is a citrus-derived natural compound that kills p53 wild-type as well as drug-resistant p53-mutant neuroblastoma cells in culture, it induces apoptosis by inhibiting N-Myc and upregulating RKIP in neuroblastoma. Didymin possesses antioxidant, anti-inflammation and anti-cancer properties.