
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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Phytantriol (mixture of isomers)
CAS:Formula:C20H42O3Purity:>95.0%(GC)Color and Shape:Colorless to Light orange to Yellow clear liquidMolecular weight:330.55Geraniol
CAS:Acyclic terpene alcoholFormula:C10H18OPurity:≥ 90.0 % (GC)Color and Shape:LiquidMolecular weight:154.252,4-Pentadienoic acid,5-(1-hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl)-3-methyl-,(2Z,4E)-
CAS:Formula:C15H20O4Purity:98%Color and Shape:SolidMolecular weight:264.3169Wilforlide a
CAS:LactoneFormula:C30H46O3Purity:≥ 98.0 % (HPLC)Color and Shape:PowderMolecular weight:454.7(R)-(-)-Carvone
CAS:Formula:C10H14OPurity:>99.0%(GC)Color and Shape:Colorless to Light yellow to Light orange clear liquidMolecular weight:150.22(1R-endo)-3-Bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
CAS:Formula:C10H15BrOPurity:98%Color and Shape:SolidMolecular weight:231.1295Cucurbitacin E
CAS:Controlled ProductCucurbitacin 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. In scientific studies, Cucurbitacin E has been extensively utilized due to its promising anticancer and anti-inflammatory properties. It has shown efficacy in inhibiting cancer cell growth and metastasis across various types, including breast, lung, and colon cancers. Additionally, its anti-inflammatory effects are leveraged in studies of inflammatory responses and disorders. Given its ability to interfere with key cellular pathways, it is a significant compound in the development of therapeutic strategies against cancer and inflammatory diseases. Researchers continue to explore its pharmacokinetics, bioavailability, and potential synergistic effects when used in combination therapies.Formula:C32H44O8Purity:Min. 95%Molecular weight:556.69 g/mol14-deoxyandrographolide
CAS:LactoneFormula:C20H30O4Purity:≥ 90.0 % (HPLC)Color and Shape:PowderMolecular weight:334.45Dihydroartemisinin
CAS:Dihydroartemisinin is an antimalarial agent, which is a semi-synthetic derivative of artemisinin. Artemisinin is a naturally occurring sesquiterpene lactone derived from the sweet wormwood plant, Artemisia annua. The mode of action of dihydroartemisinin involves the generation of free radicals within the parasite's cells. This process occurs when the endoperoxide bridge in its chemical structure reacts with iron, leading to oxidative damage and subsequent parasite death. Dihydroartemisinin is primarily used in combination therapies for the treatment of uncomplicated Plasmodium falciparum malaria. It is valued for its rapid onset of action and high efficacy against multidrug-resistant strains of P. falciparum. These qualities make it a critical component in artemisinin-based combination therapies (ACTs), which are the recommended first-line treatment for malaria in many parts of the world. The use of dihydroartemisinin, particularly in combination with partner drugs, helps prevent resistance development and enhances therapeutic outcomes.Formula:C15H24O5Purity:Min. 95%Color and Shape:White PowderMolecular weight:284.35 g/mol3-O-Acetyl-α-boswellic acid
CAS:3-O-Acetyl-alpha-boswellic acid analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Formula:C32H50O4Purity:(HPLC) ≥90%Color and Shape:PowderMolecular weight:498.75Corosolic acid
CAS:Carboxylic acid with alcohol functionFormula:C30H48O4Purity:≥ 90.0 % (HPLC)Color and Shape:PowderMolecular weight:472.71Cedryl Acetate
CAS:Formula:C17H28O2Purity:>95.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:264.41Ginsenoside Rf
CAS:Ginsenoside Rf is a steroidal saponin, which is a bioactive compound found primarily in the roots of Panax ginseng, a plant widely used in traditional medicine. As a part of the ginsenoside family, this compound exerts its effects through modulation of several cellular pathways, including anti-inflammatory and antioxidant mechanisms. It is known to interact with glucocorticoid receptors and influence calcium ion channels, contributing to its potential neuroprotective and immunomodulatory effects. In scientific research, Ginsenoside Rf is investigated for its potential applications in pharmacology, particularly regarding its role in enhancing cognitive functions and its neuroprotective properties in neurological disorders. Additionally, it is studied for its potential anti-cancer properties due to its ability to induce apoptosis and inhibit cell proliferation in certain cancer cell lines. Scientists are exploring its efficacy and safety profiles to better understand its therapeutic potential and to develop novel applications in clinical settings.Formula:C42H72O14Purity:Min. 95%Color and Shape:White PowderMolecular weight:801.03 g/molHydroxyvalerenic acid
CAS:Hydroxyvalerenic acid is a bioactive compound, which is primarily found in the roots of the Valeriana officinalis plant. This source is widely recognized in traditional medicine for its calming properties. The compound acts on the central nervous system, potentially modulating GABAergic activity, which may contribute to its sedative and anxiolytic effects. In scientific research, Hydroxyvalerenic acid is explored for its potential to support neurological function, and its application spans areas such as anxiety reduction and sleep disorder management. The complexity of its interaction with neurotransmitter systems presents opportunities for in-depth studies aimed at elucidating its biochemical pathways and therapeutic potential. Further investigations are warranted to understand its efficacy and safety profile, making it a subject of interest in neuropharmacological research.Formula:C15H22O3Purity:Min. 95 Area-%Molecular weight:250.33 g/molPseudoginsenoside f11
CAS:Natural glycosideFormula:C42H72O14Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:801.03P-cymene
CAS:Aromatic hydrocarbonFormula:C10H14Purity:≥ 95.0 % (GC)Color and Shape:LiquidMolecular weight:134.22(-)-3-Bromocamphor-8-sulfonic Acid Ammonium Salt
CAS:Formula:C10H18BrNO4SPurity:>97.0%(T)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:328.22