
Terpenoids
Terpenoids, also known as isoprenoids, are the largest class of naturally occurring organic compounds, derived from five-carbon isoprene units. They are found in a variety of plants and are known for their aromatic properties, as well as their roles in plant defense and signaling. Terpenoids have been widely studied for their therapeutic effects, including anti-inflammatory, antimicrobial, and anticancer properties. They are used in pharmaceuticals, cosmetics, and food industries for their health benefits and aromatic qualities. At CymitQuimica, you will find a wide selection of terpenoids, essential for research in plant biology, pharmacology, and natural product synthesis.
Subcategories of "Terpenoids"
- Diterpenes (C₂₀)
- Hemiterpenes (C₅)
- Monoterpenes (C₁₀)
- Sesquiterpenes (C₂₅)
- Tetraterpenes (C₄₀)
- Triterpenes (C₃₀)
Products of "Terpenoids"
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Rebaudioside A
CAS:Formula:C44H70O23Purity:>98.0%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:967.02Galbascone
CAS:Formula:C13H20OPurity:>98.0%(GC)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:192.30(-)-Isopulegol
CAS:Formula:C10H18OPurity:>98.0%(GC)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:154.25α-Terpineol
CAS:Formula:C10H18OPurity:>95.0%(GC)Color and Shape:White or Colorless to Light yellow powder to lump to clear liquidMolecular weight:154.25Cinnamodial
CAS:Cinnamodial is a naturally occurring compound classified as a sesquiterpene dialdehyde, which is isolated from cinnamon oil, derived primarily from the bark of the Cinnamomum tree. Its primary mode of action involves disrupting cellular integrity through binding with fungal cell membranes, leading to increased permeability and ultimately cell death. This mechanism highlights its potential as an effective antifungal agent. Research has shown Cinnamodial’s efficacy against a range of fungal pathogens, making it a candidate for applications in both agricultural and clinical settings. In agriculture, it can be used to manage fungal diseases in crops, enhancing yield and reducing losses. Clinically, it offers promise for the development of new antifungal therapeutics, especially in the context of rising antifungal resistance. Its natural origins also appeal to the ongoing search for biochemicals with lower environmental impact. Continued investigation into its activity spectrum, toxicity, and formulation will determine its viability for widespread use.Formula:C17H24O5Purity:Min. 95%Color and Shape:White PowderMolecular weight:308.37 g/mol(R)-(-)-Piperitone
CAS:Formula:C10H16OPurity:>94.0%(GC)Color and Shape:Light yellow to Yellow clear liquidMolecular weight:152.24Geranyl Formate
CAS:Formula:C11H18O2Purity:>55.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:182.26Digitoxose
CAS:Digitoxose is a deoxy sugar, which is an integral component of certain cardiac glycosides. These glycosides, such as digitoxin, are predominantly sourced from the leaves of the digitalis species, particularly Digitalis purpurea or Digitalis lanata. The sugar moiety, digitoxose, is critical for the glycoside's ability to exert its pharmacological effects through interactions with cellular components. The mode of action of digitoxose, once it is part of the glycoside, involves inhibiting the sodium-potassium ATPase pump in cardiac cells. This inhibition results in increased intracellular sodium, which subsequently leads to increased intracellular calcium via the sodium-calcium exchanger. Elevated calcium levels enhance cardiac contractility, making digitoxose-containing glycosides invaluable in the treatment of certain heart conditions. Digitoxose and its glycosides are primarily applied in the management of heart failure and arrhythmias, where they work to increase the force of heart contractions and maintain an appropriate rhythm. Their usage, however, requires careful dosing and monitoring due to the narrow therapeutic window and potential for toxicity.Formula:C6H12O4Purity:Min. 95%Color and Shape:Off-White Yellow PowderMolecular weight:148.16 g/mol(+)-Nerolidol
CAS:(+)-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. The mode of action of (+)-Nerolidol is attributed to its lipophilic nature, which allows it to penetrate cellular membranes easily. This property enables interactions with various biological targets, leading to its diverse biological activities. It has been investigated for its potential effects on microbial activity, antioxidant properties, and as a skin penetration enhancer. The applications of (+)-Nerolidol are broad, with studies indicating its utility in pharmaceutical, cosmetic, and agricultural sectors. In pharmaceuticals, it holds promise as an antifungal, antimicrobial, and anticancer agent. In cosmetics, it may function as a fragrance additive and a skin absorption enhancer for other active ingredients. Additionally, in agriculture, its role as an insect repellent and natural pesticide is being explored. The versatility of (+)-Nerolidol continues to make it a compound of interest in various scientific domains.Formula:C15H26OPurity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:222.37 g/mol2-Isopropenyl-5-methyl-5-vinyltetrahydrofuran (mixture of isomers)
CAS:Formula:C10H16OPurity:>97.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:152.24Cannabichromevarinic acid
CAS:Carboxylic acid with phenol functionFormula:C20H26O4Purity:≥ 98.0 % (HPLC)Color and Shape:PowderMolecular weight:330.42Triptophenolide
CAS:Triptophenolide is a bioactive compound, which is a diterpenoid lactone extracted from the plant Tripterygium wilfordii. This compound is characterized by its ability to modulate various molecular targets and pathways associated with inflammation and immune response. The mode of action of triptophenolide involves the inhibition of nuclear factor kappa B (NF-κB) signaling, a pivotal transcription factor that regulates genes involved in inflammation, immunity, cell proliferation, and survival. By disrupting NF-κB activity, triptophenolide effectively decreases the expression of pro-inflammatory cytokines and other mediators. Triptophenolide is primarily used in research settings to explore its effects on diseases characterized by excessive inflammatory responses, such as autoimmune disorders and certain types of cancer. Its unique mechanism and plant-derived origin make it a compound of interest in the development of new therapeutic strategies. While its potent biochemical interactions underscore significant therapeutic potential, further studies are required to fully elucidate its efficacy and safety profiles in clinical applications.Formula:C20H24O3Purity:Min. 95%Molecular weight:312.4 g/molAlantolactone
CAS:Alantolactone is a bioactive sesquiterpene lactone, which is derived from the roots of Inula helenium, a plant commonly known as elecampane. This compound is characterized by its complex bicyclic structure and exhibits a range of biological activities. The mode of action of alantolactone involves multiple biochemical pathways, including the inhibition of nuclear factor kappa B (NF-κB) and the modulation of reactive oxygen species (ROS) production. These pathways contribute to its anti-inflammatory, anti-cancer, and antimicrobial properties. In scientific research, alantolactone is utilized for its potential therapeutic benefits. It is studied for its anti-cancer effects, particularly in inducing apoptosis and inhibiting proliferation in various cancer cell lines. Additionally, its anti-inflammatory properties make it a subject of interest for treating inflammatory diseases. The compound also possesses antimicrobial activity, adding to its versatility in pharmacological research. The exploration of alantolactone’s diverse bioactivities continues to provide valuable insights into its mechanisms, offering potential applications in drug development.Formula:C15H20O2Purity:Min. 95%Color and Shape:PowderMolecular weight:232.32 g/molCryptotanshinone
CAS:Formula:C19H20O3Purity:>97.0%(HPLC)Color and Shape:Orange to Brown powder to crystalMolecular weight:296.37Prosaikogenin H
CAS:Prosaikogenin H is a naturally occurring compound, classified as a saponin, which is derived from specific plant sources, particularly within the family Araliaceae. It is obtained through extraction and purification processes from plants known for their bioactive compounds. The mode of action of prosaikogenin H involves interacting with cellular pathways to modulate biological responses, including anti-inflammatory and antioxidant effects. These interactions are facilitated by its structural properties that enable it to engage with cell membranes and influence signaling cascades. Prosaikogenin H is primarily used in research focused on exploring therapeutic potentials, particularly in the development of treatments for inflammatory conditions and oxidative stress-related disorders. It serves as a valuable compound in pharmacological studies aiming to discover novel therapeutic agents. Its applications extend to cellular and molecular biology research, where it may be used to elucidate biological mechanisms and pathways relevant to its activity. As such, prosaikogenin H stands out in scientific investigations for its promising role in advancing our understanding of plant-derived bioactive compounds in health sciences.Formula:C36H58O8Purity:Min. 95%Molecular weight:618.84 g/mol(4S)-4-Ethyl-4-hydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione
CAS:Formula:C20H16N2O4Purity:95%Color and Shape:SolidMolecular weight:348.35203999999993Caryophyllene Oxide 1000 µg/mL in Isopropanol
CAS:Formula:C15H24OColor and Shape:Single SolutionMolecular weight:220.35Olean-12-ene-23,28-dioic acid, 3-(β-D-glucopyranosyloxy)-2,27-dihydroxy-, (2β,3β,4α)-
CAS:Formula:C36H56O12Purity:95%Color and Shape:SolidMolecular weight:680.8226