Fenilpropanóides

Lactone

Natural glycoside

Phenol alcohol

Polyphenol

Lactone

3,5-Dicaffeoylquinic acid is a polyphenolic compound, which is naturally found in various plant species, particularly in coffee and certain herbal plants. This compound serves as a secondary metabolite within these plants, contributing to their defense mechanisms against pathogens and environmental stress. The compound exhibits its mode of action primarily through its powerful antioxidant activity. By scavenging free radicals and inhibiting oxidative stress pathways, it helps in protecting cellular components from oxidative damage.

Sinapaldehyde is a phenolic aldehyde, which is a secondary metabolite derived from lignin biosynthesis in plants. It is primarily sourced from lignin, a complex polymer found in the cell walls of various plants, often extracted through biochemical refinement processes from lignocellulosic biomass. The mode of action of Sinapaldehyde involves its function as an antioxidant, where it participates in redox reactions that mitigate oxidative stress by scavenging free radicals. Its structural characteristics enable it to interact with various biological molecules, contributing to its effectiveness in these reactions.

Resveratrol is a natural phenylpropanoid of the family of stilbenoids and is present in red wines and certain foods. Resveratrol has been deeply studied for its antioxidant, anti-inflammatory and antimicrobial properties. In Vero cells, resveratrol at 50 μM has shown to have the ability to inhibit SARS-CoV-2 replication by 98% when added after infection. Featured reference paper: Rossi et al, 2021; Yang et al, 2021.

<p>3,4-Dicaffeoylquinic acid is a naturally occurring polyphenolic compound, which is predominantly found in various plants and herbal sources such as artichokes, echinacea, and certain species of coffee. Its structure consists of quinic acid esterified with two caffeic acid moieties, making it a member of the chlorogenic acid family. This compound is well-recognized for its potent antioxidant properties, exerting its effects by scavenging free radicals and reducing oxidative stress within biological systems.</p>

<p>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).</p>

Podophyllotoxin is a potent antimitotic agent, which is derived from the roots and rhizomes of plants belonging to the genus Podophyllum, such as Podophyllum peltatum and Podophyllum emodi. Its mode of action involves the inhibition of microtubule assembly, leading to the disruption of mitotic spindle formation during cell division. This results in the arrest of cell proliferation, making it particularly effective against rapidly dividing cells.

<p>Malabaricone A is a naturally occurring compound, which is a diarylnonanoid isolated from the fruits of Myristica malabarica, commonly known as the Malabar nutmeg tree. This compound exhibits diverse biological activities due to its unique chemical structure, primarily contributing to its mode of action as an antioxidant and anti-inflammatory agent. Malabaricone A scavenges free radicals and modulates cellular pathways involved in the inflammatory response, making it a potential therapeutic candidate in the management of oxidative stress-related disorders.</p>

<p>Malabaricone C is a bioactive compound which is extracted from the roots of trees belonging to the genus Myristica. These trees are well-known for producing a diverse array of secondary metabolites with unique biological activities. Derived primarily through careful extraction processes from these natural sources, Malabaricone C has been characterized by its distinct ability to modulate inflammatory pathways and exhibit antimicrobial properties. The compound is known to interfere with specific biochemical targets, potentially inhibiting the expression of pro-inflammatory cytokines and disrupting microbial cell mechanisms.</p>

<p>4,5-Dicaffeoylquinic acid is a polyphenolic compound, which is primarily a derivative of chlorogenic acids found in various plants, notably within the Asteraceae family. It is naturally sourced from leaves, fruits, and other plant tissues where it plays a critical role in the plant's defense mechanisms. It functions through its ability to scavenge free radicals, thereby exhibiting significant antioxidant activity. This compound can inhibit oxidative stress by neutralizing reactive oxygen species (ROS), thus protecting cellular structures from damage.</p>

<p>Antioxidant; anti-inflammatory; anti-cancer agent; HSP90 inhibitor</p>

<p>Malabaricone B is a bioactive compound, which is a phenolic compound sourced from the seeds of the Myristica malabarica plant, commonly known as Indian bay leaf. This compound exhibits significant pharmacological activity, particularly in its ability to inhibit various inflammatory mediators.</p>

<p>Dimethylcurcumin is a synthetic, small-molecule compound that is a derivative of curcumin, a naturally occurring polyphenol found in the spice turmeric. Curcumin is known for its various biological activities, but its clinical use is limited due to poor bioavailability. Dimethylcurcumin is chemically modified to enhance its stability and bioavailability, making it a more potent alternative.</p>

Neohesperidin dihydrochalcone hydrate is a high-intensity sweetener, which is derived from the bitter flavonoids found in citrus fruits, particularly from the peel and pulp of oranges and grapefruits. It is produced through a chemical hydrogenation process that transforms neohesperidin into a non-caloric sweetener. This unique compound acts as a potent flavor enhancer by intensifying sweetness and masking undesirable flavors, such as bitterness.

(+)-Dehydrodiconiferyl alcohol is a lignan, which is a type of phenolic compound naturally occurring in a variety of plant species, including those in the families Magnoliaceae, Lauraceae, and others. As a secondary metabolite derived from the oxidative coupling of coniferyl alcohol, it plays roles in plant defense and structural integrity.

<p>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.</p>