Terpenoids

Esculentoside H is a naturally occurring triterpenoid saponin, which is derived from the plant Phytolacca esculenta, commonly known as the pokeweed. This compound has garnered significant interest due to its unique mode of action as an anti-inflammatory and immunomodulatory agent. By modulating cellular signaling pathways, Esculentoside H can inhibit the expression of pro-inflammatory cytokines and suppress the activation of NF-kB, a key transcription factor involved in inflammatory responses.

Prosaikogenin G is a saponin derivative, which is a bioactive compound commonly found in medicinal plants, traditionally used in Eastern medicine. Saponins are naturally occurring glycosides, and they have a wide range of biological activities due to their amphiphilic nature. Prosaikogenin G is specifically sourced from Bupleurum species, a well-known genus in herbal medicine. These compounds have been extensively studied for their anti-inflammatory and immunomodulatory effects.

Congmunoside V is a triterpenoid saponin, which is a bioactive compound isolated from the plant Gynostemma pentaphyllum, also known as Jiaogulan. This plant is traditionally recognized in herbal medicine and is a member of the Cucurbitaceae family, primarily found in East Asia. Triterpenoid saponins are a class of chemical compounds composed of a sapogenin (triterpene) attached to sugar moieties, which confer a variety of biological activities.

Illudin S is a sesquiterpene toxin, which is a naturally occurring compound isolated from several species of fungi belonging to the genus Omphalotus, such as Omphalotus olearius, commonly known as the Jack-o'-lantern mushroom. Its mode of action involves alkylating DNA, which leads to DNA cross-linking and subsequent inhibition of DNA synthesis. This mechanism renders it highly cytotoxic, as it can induce cell death by disrupting normal cellular replication processes.

Cycloartenol acetate is a natural triterpenoid, which is primarily derived from plant sources. It serves as a key intermediate in the biosynthesis of sterols, crucial components of plant cell membranes. The compound is synthesized in the plant's cellular systems through the cyclization process from 2,3-oxidosqualene, utilizing cycloartenol synthase enzymes. This enzymatic modification marks the diverging point between plant sterol and steroid biosynthesis pathways, distinguishing it from similar pathways in animals and fungi.

Flavour and scent of grapefruit

Escin Ib is a natural saponin glycoside, which is derived from the seeds of Aesculus hippocastanum, commonly known as horse chestnut. Its mode of action involves inhibiting the enzyme hyaluronidase, thereby reducing capillary permeability and effectively controlling edema and inflammation. Additionally, it acts by stabilizing lysosomal membranes, further contributing to its anti-inflammatory effects.

Pinifolic acid is a bioactive compound, which is derived from Pinus sylvestris (Scots pine), a species of pine native to Eurasia. This compound is extracted from the needles and bark of the tree, recognized for its rich content of polyphenolic compounds. The mode of action of pinifolic acid involves potent antioxidant activity, which is facilitated by its ability to scavenge free radicals and thereby reduce oxidative stress at the cellular level. The bioactive components are believed to interact with various biochemical pathways, potentially exerting anti-inflammatory and protective effects on various tissues.

Cimigenol is an acetate extract from the plant Cimicifuga foetida. This extract has been shown to have antiproliferative and anticomplement activities, as well as a pharmacokinetic profile that is similar to epinephrine. It has been shown to induce autophagy in prostate cancer cells and inhibit the growth of fetal bovine retinal pigment epithelium cells. The mechanism of action of cimigenol is not yet known, but it may involve hydroxyl group reactions with proteins or epidermal growth factor (EGF) receptors on cell surfaces. Cimigenol also has anticancer properties that are mediated by its ability to reduce mitochondrial membrane potential (MMP).
CIMIGENOL- A potent acetate extract from the plant Cimicifuga foetida, which has been shown to have antiproliferative and anticomplement activities, as well as a pharmacokinetic profile that is similar to

Tripdiolide is a bioactive diterpenoid, which is derived from the Chinese medicinal plant Tripterygium wilfordii, commonly known as Thunder God Vine. This compound exerts its effects through a complex mode of action, primarily involving the inhibition of nuclear factor kappa B (NF-kB) signaling pathways and the induction of apoptosis. Recent studies have also suggested its role in modulating the immune response by targeting specific cytokines and signaling pathways.

QS-21 is a saponin-based adjuvant, which is a compound used to enhance the body's immune response to an antigen. This product is derived from the bark of the Quillaja saponaria tree, commonly known as the soapbark tree, native to Chile. The mode of action of QS-21 involves stimulating the immune system by activating antigen-presenting cells, such as dendritic cells and macrophages, which in turn enhance both humoral and cellular immune responses.

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

Isocalendin is a natural compound derived from the calendula plant, known for its potent anti-inflammatory properties. This product is extracted through a meticulous process that maintains the bioactive compounds inherent to calendula, ensuring efficacy and purity. Isocalendin functions by modulating inflammatory pathways at the cellular level, primarily inhibiting pro-inflammatory mediators. This selective action aids in reducing inflammation and promoting tissue repair without adverse effects associated with synthetic alternatives.

Inhibits canonical Wnt/β-catenin signaling; antineoplastic

Agnuside is a diterpenoid compound, which is a phytoconstituent primarily sourced from the plant Vitex agnus-castus, commonly known as chaste tree. This compound is extracted from the fruit of the plant through a series of isolation and purification processes aimed at preserving its chemical integrity.

Escin sodium is a phytopharmaceutical agent, which is a derivative of the saponin complex found in the seeds of the horse chestnut tree, Aesculus hippocastanum. Its mode of action involves anti-inflammatory and vasoactive processes, primarily exerted through reducing vascular permeability and increasing venous tone. These mechanisms facilitate the reduction of edema and improve venous return.

Bilobalide is a sesquiterpene trilactone, which is a secondary metabolite isolated from the leaves of the Ginkgo biloba tree. The source of bilobalide, Ginkgo biloba, is one of the oldest tree species, extensively studied for its wide array of bioactive compounds. Bilobalide exerts its mode of action predominantly through modulation of various neurotransmitter systems and protection against neuronal injury. It has demonstrated the ability to antagonize the GABAA receptor and inhibit excitotoxicity related to excessive glutamate release, thereby providing neuroprotective effects.

Zederone is a bioactive sesquiterpene, which is a type of terpenoid compound. It is primarily sourced from the rhizomes of several Curcuma species, particularly Curcuma zedoaria. These plants are native to regions of Asia and have been used in traditional medicine for various purposes.

Secondary plant metabolite with antimicrobial properties produced in response to plant infection and exposure to UV light. This diterpenoid phytoalexin is found only in rice (Oryza sativa) and moss (Hypnum plumaeforme).

Gnidimacrin is a natural diterpenoid ester, which is derived from the plant genus *Gnidia*. It is known for its intricate molecular structure and potent biological activities. As a plant-derived compound, it is sourced primarily from the shrubs native to Africa and Asia, belonging to the Thymelaeaceae family.

Isosteviol is a diterpenoid compound, which is a metabolite derived from the enzymatic hydrolysis of stevioside, a glycoside found in the leaves of the Stevia rebaudiana plant. Its mode of action involves modulation of various biological pathways, including anti-inflammatory and antihyperglycemic effects. These actions are attributed to its ability to interact with specific cellular targets, inhibiting pro-inflammatory cytokines and improving insulin sensitivity.

Selective antibacterial and anti-inflammtory activity; uterine relaxant

Iriversical is a synthetic compound, which is derived from a combination of bioactive organic molecules. It operates through intricate biochemical interactions, specifically targeting cellular pathways involved in signal transduction. These interactions are facilitated by the compound's affinity for binding sites on specific enzymes, thereby modulating their activity.

Ginkgolide B is a diterpenoid lactone, which is a secondary metabolite isolated from the leaves of the Ginkgo biloba tree. This compound is primarily sourced from the extract of Ginkgo biloba, a plant that has been utilized for centuries in traditional medicine systems.

10-epi-Elemol is a sesquiterpene alcohol, which is derived from natural plant sources, primarily obtained through the essential oils of particular species. Its molecular structure includes a complex arrangement of carbon rings and an alcohol group, characterizing it as a prominent component among sesquiterpenes.

Ginsenoside Rh3 is a bioactive saponin compound, which is a principle component isolated from Panax ginseng, a perennial plant widely known for its medicinal properties. This compound represents a specific form of ginsenoside with distinct pharmacological characteristics derived through the deglycosylation process of other ginsenosides during processing or digestion.

Cryptotanshinone is a naturally occurring bioactive compound, which is an abietane diterpenoid sourced from the roots of *Salvia miltiorrhiza*, commonly known as Danshen. This compound exhibits a distinct mode of action characterized by its inhibition of the STAT3 signaling pathway, which is crucial in the regulation of gene expression involved in cell growth and survival. Furthermore, Cryptotanshinone demonstrates the ability to modulate various other molecular targets, such as the androgen receptor, rendering it valuable in the pharmacological landscape.

Momordin 1c is a triterpenoid saponin, a type of secondary metabolite, extracted primarily from species of the plant genus *Momordica*, such as *Momordica charantia*—commonly known as bitter melon. This compound is characterized by its unique structure, which contributes to its biological activities.

Picrotin is a natural compound, which is derived from the Anamirta cocculus plant, commonly known as the Indian berry or fishberry. It belongs to the class of sesquiterpene lactones, which are known for their complex structures and bioactivity. The mode of action of picrotin primarily involves interactions with the central nervous system, although the exact molecular targets are not fully elucidated. Studies suggest that it may act as a GABA receptor antagonist, which can influence neurotransmitter activity.

Lnuchinenolide B is a bioactive compound, which is a type of natural product often isolated from various plant species. This compound has garnered interest due to its origins in diverse botanical sources. Its mode of action is typically associated with its interaction at the molecular level with specific biological targets, potentially inhibiting or modulating particular enzymatic activities or receptor pathways. Such interaction underscores its capacity to influence biological processes, making it a compound of interest in pharmacological research.

(-)-Perillyl alcohol is a monoterpene alcohol, which is a naturally occurring compound primarily extracted from the essential oils of lavender, peppermint, and other plants in the Lamiaceae family. It is characterized by its ability to interfere with cellular processes, notably through its modulation of signaling pathways and induction of apoptosis, as well as inhibition of cell proliferation.

Volvalerenic acid is a sesquiterpene compound, which is a naturally occurring organic constituent found in the roots of Valeriana species, particularly Valeriana officinalis. This compound is primarily obtained through the extraction of these roots utilizing organic solvents and further chromatographic purification methods.

Deoxygedunin is a natural limonoid, which is a type of chemical compound often derived from plant sources, particularly in the Meliaceae family. This compound is primarily isolated from the seeds of the Indian neem tree (Azadirachta indica) and the African mahogany tree (Khaya senegalensis). It exhibits its biological effects through activation of the Nrf2 pathway, an essential cellular defense mechanism against oxidative stress. By promoting the expression of antioxidant proteins, deoxygedunin enhances cellular resilience to oxidative damage.

Valencene is a sesquiterpene, which is a naturally occurring terpenoid hydrocarbon. It is primarily sourced from the essential oils of citrus fruits, particularly Valencia oranges. Its mode of action involves its volatile nature, which contributes to its distinctive, sweet, citrusy aroma. Valencene is often synthesized or extracted using advanced biotechnological methods, ensuring high purity and consistency.

Gedunin is a pentacyclic triterpenoid compound which is primarily found in the neem tree (Azadirachta indica) and other plants in the Meliaceae family.Gedunin works by inhibiting heat shock proteins (Hsp), which are involved in protein folding and stress responses in cells. It also triggers apoptosis in cancer cells and modulates inflammatory pathways to reduce inflammation.Gedunin is used for its anticancer, antimalarial, antibacterial, antifungal, anti-inflammatory, and neuroprotective properties. It has shown promise in inducing apoptosis in cancer cells, effectively combating malaria parasites, exhibiting antimicrobial properties, reducing inflammation, and potentially benefiting neurodegenerative diseases like Parkinson's.

Cineole, often referred to as eucalyptol, is a monoterpenoid and a cyclic ether that represents a key constituent of certain essential oils. It is primarily sourced from the leaves of Eucalyptus species, but also found in smaller quantities within other aromatic plants such as rosemary, sage, and tea tree. Cineole exerts its effects through a multifaceted mode of action, acting predominantly as an antimicrobial and anti-inflammatory agent. This is achieved by disrupting the lipid membrane of microbial pathogens, leading to their destabilization and eventual demise. Additionally, cineole modulates inflammatory pathways by inhibiting the production of pro-inflammatory cytokines, thereby ameliorating symptoms associated with inflammation.

Toosendanin is a bioinsecticidal compound, which is a natural product isolated from the bark of the Melia toosendan tree, also known as the Chinese Melia. The source of this compound lies in the Meliaceae family, known for its diverse array of bioactive phytochemicals.

(1S)-(-)-(-)-Verbenone is a bicyclic monoterpene, which is a type of terpenoid compound. It is naturally sourced from various plants, predominantly from the essential oils of pines and other coniferous trees. The mode of action of Verbenone is intriguing; it acts as an anti-aggregation pheromone in certain beetle species, disrupting their communication and reducing infestation levels. This mechanism is particularly effective against bark beetles, which are known to cause significant damage to forestry ecosystems.

Cucurbitacin E is a triterpenoid compound, which is a natural product derived from plants in the Cucurbitaceae family. This bioactive compound exerts its effects primarily through the disruption of cytoskeletal integrity, inhibition of the JAK/STAT signaling pathway, and induction of apoptosis. These molecular activities make it a potent agent in research focusing on cellular proliferation and inflammation.

(+)-Nerolidol is a sesquiterpene alcohol, which is a type of volatile organic compound. It is derived from the essential oils of various plants, including jasmine, tea tree, and lemongrass. As a natural compound, (+)-Nerolidol is synthesized by plants as part of their aromatic profile and may serve as a defense mechanism against pathogens and herbivores.

14-Epitriptolide is a diterpenoid epoxide, which is derived from the natural product triptolide. It originates from the plant species *Tripterygium wilfordii*, commonly known in traditional Chinese medicine. The mode of action of 14-Epitriptolide involves the inhibition of RNA polymerase II-mediated transcription, thereby interfering with transcriptional processes essential for cancer cell survival and proliferation. Additionally, it induces oxidative stress and disrupts cellular homeostasis.

Saikosaponin C is a triterpene saponin, which is a bioactive compound found in various medicinal plants, particularly those in the genus Bupleurum, often used in traditional Chinese medicine. It is derived from the roots of these plants, where it coexists with other saponins, contributing to their medicinal properties.

Loganin is a bioactive iridoid compound, which is a type of secondary metabolite typically found in plants. It is primarily derived from sources such as the genera Strychnos and Gentiana, among others. Loganin operates through various biological pathways, influencing enzymatic and receptor activities that contribute to its pharmacological effects. These activities include anti-inflammatory, antioxidant, and neuroprotective actions, making Loganin a compound of interest in several areas of medical research.

Ursolic acid acetate is a natural triterpenoid compound, which is derived from the acetylation of ursolic acid. This compound is sourced from a variety of medicinal plants, including apples, rosemary, and holy basil. Its mode of action involves modulating multiple cellular pathways, including the inhibition of nuclear factor-kappa B (NF-κB) and the activation of AMP-activated protein kinase (AMPK). These actions contribute to its anti-inflammatory, anticancer, and antioxidant properties.

Soyasaponin III is a bioactive compound, which is a naturally occurring saponin derived from soybeans. These glycosides are primarily found in the seeds of the soybean plant, Glycine max. Soyasaponins are known for their amphiphilic nature, which enables them to interact with both lipid and aqueous phases, affecting membrane dynamics and cellular processes.

α-Amyrin is a pentacyclic triterpene, which is commonly found in the resins and latex of various plant species. It is primarily sourced from the lipophilic extracts of angiosperms, where it is often present in both the free form and as esters. Its mode of action involves modulation of key signaling pathways involved in inflammation and cellular oxidative stress, particularly through the inhibition of pro-inflammatory enzymes such as cyclooxygenase. α-Amyrin also induces apoptosis via mitochondrial pathways in certain cell types, adding to its therapeutic potential.

Triptophenolide methyl ether is a bioactive compound, classified as a terpene, derived from natural plant sources. It is primarily isolated from the roots of species within the *Tripterygium* genus. Terpenes are a large and varied class of organic compounds produced by a variety of plants, known for their aromatic qualities and biological activity.