Lignans

(-)-Arctigenin is a lignan compound, which is naturally derived from certain plant species, primarily found in the seeds of Arctium lappa, commonly known as burdock. The compound exhibits a diverse mode of action, primarily noted for its ability to inhibit the proliferation of cancer cells through apoptosis induction, cell cycle arrest, and modulation of various signaling pathways. Additionally, it exerts antiviral effects by targeting viral replication processes and exhibits anti-inflammatory properties by downregulating pro-inflammatory cytokines. The uses and applications of (-)-Arctigenin are varied and significant in biomedical research. It is extensively studied for its potential as an anticancer agent across various types of malignancies, including breast and lung cancers. Due to its antiviral properties, it has been evaluated in the context of infections caused by viruses such as HIV and influenza. Additionally, its anti-inflammatory effects have led to investigations into its potential use in treating inflammatory-related diseases. As a compound of interest in natural product chemistry and pharmacology, (-)-Arctigenin serves as a promising candidate for developing novel therapeutic agents.

Oxygen-heterocyclic compound

Oxygen-heterocyclic compound

Technical grade is a natural from Magnolia sieboldii

Taiwanin C, a lignan from Cryptocarya chinensis, boasts anti-inflammatory, antioxidant, and anticancer properties.

Enterodiol is a phytoestrogenic compound, specifically classified as a plant-derived lignan metabolite, which originates from the consumption and subsequent gut microbial transformation of lignans found in dietary fiber-rich foods such as flaxseeds, whole grains, and certain vegetables. The mode of action involves its conversion by intestinal microbiota into enterodiol from precursors such as secoisolariciresinol diglucoside. Once absorbed, enterodiol can interact with estrogen receptors, exhibiting weak estrogenic activity, which contributes to its role as a selective estrogen receptor modulator. Enterodiol's potential uses and applications are diverse, spanning areas of interest such as hormonal modulation, cancer prevention, and cardiovascular health. Due to its ability to emulate estrogen albeit with much weaker potency, it plays a role in mitigating symptoms associated with low estrogen levels, such as those experienced during menopause. Additionally, its antioxidant properties contribute to the reduction of oxidative stress, supporting its examination in studies focused on chronic disease prevention. Current research emphasizes the need to explore its efficacy, bioavailability, and long-term effects to fully understand its implications and potential therapeutic uses within clinical settings.

(-)-Syringaresinol diglucoside is a naturally occurring lignan glycoside, which is predominantly found in certain plant species, such as the roots of Eleutherococcus senticosus (Siberian ginseng) and other similar sources. This compound is categorized as a phytoestrogen due to its ability to elicit weak estrogenic activity by binding to estrogen receptors, which may influence various biological processes. (-)-Syringaresinol diglucoside’s mode of action includes its antioxidant and anti-inflammatory properties. It may modulate the oxidative stress pathways and inflammatory responses, offering potential protective effects against certain diseases. By interfering with specific signaling pathways, it might also demonstrate anti-cancer and anti-viral activities, although more research is needed to fully elucidate these mechanisms. The applications of (-)-Syringaresinol diglucoside extend to various fields of scientific research, including studies focused on its potential therapeutic effects and elucidating its role in plant biochemistry and ecology. Its presence in traditional medicinal plants also underscores its significance in ethnobotanical and pharmacological studies. Current research might investigate its impact on human health, particularly in the context of metabolic disorders and hormone-related conditions.

Podophyllotoxinone, a natural compound found in Dysosma versipellis, shows inhibitory activity against L1210 leukemia and KB cells in vitro.

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

Gomisin J is a natural product and have vasodilatory activity.

(+)-Lyoniresinol 9'-O-glucoside is a compound obtained from the root bark of Lycium barbarum with antimicrobial antioxidant activity activity.

Lactone

Etoposide is a chemotherapy medication used for the treatments of a number of types of cancer. Etoposide inhibits DNA synthesis by forming a complex with topoisomerase II and DNA, it induces apoptosis in MCF-7 breast cancer cells.

Salvadoraside is a glycosylated natural compound, which is derived from the plant Salvadora persica, commonly known as the toothbrush tree. This compound is primarily extracted from the stems and roots of the plant. Its mode of action involves a variety of biochemical pathways, including potential antioxidative, antimicrobial, and anti-inflammatory activities. Salvadoraside interacts with cellular pathways by modulating the expression of specific enzymes and receptors, offering promising avenues in medicinal chemistry. The uses and applications of Salvadoraside are currently being explored in various scientific studies, focusing on its efficacy in dental health due to its natural antimicrobial properties. Furthermore, it is being investigated for broader therapeutic potential, including roles in managing oxidative stress and contributing to inflammatory response regulation. As research progresses, Salvadoraside's contribution to pharmacology could span multiple disciplines, offering insights into novel drug development and natural product chemistry.

Lactone

Matairesinoside is a naturally occurring phenolic compound, which is primarily extracted from certain plant species known for their medicinal properties, such as the Daphne genus. It functions through modulation of various biochemical pathways, exhibiting antioxidant, anti-inflammatory, and potential anti-cancer activities. These actions are mediated via its ability to scavenge free radicals, inhibit pro-inflammatory cytokines, and modulate cellular apoptosis pathways. In a scientific context, Matairesinoside is being explored for its potential therapeutic applications. Its antioxidant activity makes it a candidate for protecting cells against oxidative stress-related damage, which is implicated in aging and various chronic diseases. The compound's anti-inflammatory properties offer potential in the treatment of inflammatory disorders. Furthermore, preliminary studies suggest that Matairesinoside may exert anti-cancer effects by inhibiting tumor growth and inducing apoptosis in certain cancer cell lines. Current research is focusing on its detailed mechanisms of action, bioavailability, and efficacy in various model systems. Overall, Matairesinoside represents a promising molecule for further investigation in the field of pharmacology and therapeutic development.

Phillyrin is a lignan compound, which is a bioactive chemical derived from the seeds and fruits of the plant Forsythia suspensa, a traditional medicinal herb. This compound is recognized for its multifaceted mode of action, primarily through its anti-inflammatory, antioxidant, and antimicrobial properties. Phillyrin functions by modulating signaling pathways, inhibiting oxidative stress, and suppressing pro-inflammatory cytokine production, making it significant in the field of pharmacology. Phillyrin's applications are diverse, extending into therapeutics for conditions characterized by inflammation and oxidative stress. Researchers have demonstrated its potential in mitigating diseases such as arthritis, cardiovascular disorders, and microbial infections. Furthermore, its ability to scavenge free radicals makes it valuable in studies aimed at understanding aging and age-related diseases. The compound's pharmacological benefits are continually being explored in preclinical and clinical settings, highlighting its promise as a candidate for drug development in the management of chronic inflammatory and oxidative-dependent ailments.

Oxygen-heterocyclic compound

Natural glycoside

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

Prestegane B is a bioactive compound, which is a natural product extracted from the plant Hewittia sublobata. This compound is sourced from the leaves and stems of the plant, which have been traditionally used in various folk medicines. The extraction process involves detailed phytochemical analysis to isolate the active constituents. Prestegane B operates by modulating specific biochemical pathways, particularly by interacting with cellular receptors and enzymes, ultimately influencing cellular processes and signaling cascades. This mode of action suggests potential applications in modulating inflammatory responses or acting as an antioxidant. The uses and applications of Prestegane B are primarily in the field of medicinal research, where it holds promise as a lead compound for drug development in treating various ailments. Its pharmacological profile is being explored for its efficacy in neurological, anti-inflammatory, and antioxidative contexts. Ongoing studies aim to elucidate its full therapeutic potential and underlying mechanisms, contributing valuable insights to the field of natural product research and pharmacognosy.

Carboxylic acid with additional oxygen functions

Natural glycoside

Please enquire for more information about Chicanin including the price, delivery time and more detailed product information at the technical inquiry form on this page

Oxygen-heterocyclic compound

Phyllanthin is widely used as hepatoprotective and antigenotoxic and inhibit function of P-gp.

Natural glycoside

Deoxypodophyllotoxin shows cytotoxic , antineoplastic, antitumor, insecticidal, anti-angiogenic, vascular disrupting, insecticidal, antiviral, and anti-inflammatory activities. Deoxypodophyllotoxin induces G2 /M cell-cycle arrest followed by apoptosis through multiple cellular processes, involving the activation of ATM, upregulation of p53 and Bax, activation of caspase-3 and -7, and accumulation of PTEN resulting in the inhibition of the Akt pathway. Deoxypodophyllotoxin maybe applicable to treat hyperpigmentation, it decreases UV-induced skin pigmentation of brown guinea pigs.

Epimagnolin A is a lignan obtained from the flower buds of Magnolia fargesii, which is traditionally used in Asian medicine for treating headache and nasal

Oxygen-heterocyclic compound

Fargesin is a naturally occurring compound that is a bioactive constituent of Magnolia flowers. It is derived from the dried buds of Magnolia fargesii, a plant traditionally used in herbal medicine. The compound exhibits a mode of action that involves anti-inflammatory and anti-allergic properties. It operates through the inhibition of the release of pro-inflammatory mediators, thereby reducing inflammation and allergic responses. Fargesin finds its applications primarily in the management of sinusitis and other respiratory tract ailments. Its anti-inflammatory effects make it a valuable molecule in reducing nasal congestion, sinus pressure, and other symptoms associated with rhinitis and sinus infections. Given its natural origin and targeted action, Fargesin is of interest in the development of treatments that aim to alleviate allergic and inflammation-related conditions without the side effects commonly associated with synthetic drugs. Researchers are exploring its potential uses in broader therapeutic contexts, contributing to a growing body of literature on botanical extracts in medical science.