Phenylpropanoids

Lactone

Natural glycoside

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

1,5-Dicaffeoylquinic acid is a polyphenolic compound, which is naturally occurring in various plants, including artichokes and coffee. This compound is part of a larger group of chlorogenic acids that are esterified products of caffeic acid and quinic acid. The mode of action of 1,5-dicaffeoylquinic acid involves its ability to scavenge free radicals, thereby exhibiting potent antioxidant activity. Additionally, it modulates signaling pathways involved in inflammation, contributing to its anti-inflammatory effects. The compound has been extensively studied for its potential health benefits and therapeutic applications. It is commonly used in research focusing on its role in protecting against oxidative stress-related diseases, such as cardiovascular diseases and neurodegenerative disorders. Moreover, 1,5-dicaffeoylquinic acid is investigated for its application in the development of nutraceuticals and functional foods aimed at enhancing human health through diet. Its diverse biological activities continue to attract scientific interest, highlighting its importance in both basic and applied research settings.

1,3-Dicaffeoylquinic acid is a bioactive compound, which is a type of caffeoylquinic acid. This compound is commonly found in various plant sources, including coffee, artichokes, and certain herbal extracts. It is part of a larger family of polyphenolic compounds that are notable for their diverse biological activities. The mode of action of 1,3-Dicaffeoylquinic acid primarily involves its antioxidant properties. It scavenges free radicals and protects cells from oxidative stress by neutralizing reactive oxygen species. This activity is essential in preventing lipid peroxidation and in maintaining cellular integrity under stress conditions. 1,3-Dicaffeoylquinic acid is used extensively in scientific research for its potential health benefits, including anti-inflammatory and hepatoprotective effects. It is studied for its role in modulating biological pathways related to metabolic disorders and neuroprotection. Additionally, it has applications in the formulation of nutraceuticals and functional foods, where its ability to enhance antioxidant defenses and improve cellular health is of significant interest. Its presence in widely consumed beverages like coffee also invites investigations into its potential contributions to human health in dietary contexts.

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

This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Methyl rosmarinate shows antioxidative, and antifungal activities. It has inhibitory activities against tyrosinase, α-glucosidase, and matrix metalloproteinase-1 (MMP-1).

Carboxylic acid with additional oxygen functions

Oxygen-heterocyclic compound

This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Cryptochlorogenic acid is an isomer of chlorogenic acid and is found in plants. Cryptochlorogenic acid is the major component of the extract of mulberry leaves that is traditionally used to treat diabetes mellitus. In a diabetic model in rats, cryptochlorogenic acid alleviated symptoms, such as, blood glucose levels, accumulation of lipid peroxides, and iron content alterations. In vitro studies with RAW 264.7 macrophages, cryptochlorogenic acid showed antioxidant and anti-inflammatory activity by increasing both the cellular content of reduced glutathione, and the expression of superoxide dismutase activity, while inhibiting the nuclear translocation of the nuclear factor erythroid 2–related factor 2 (Nrf2).