
Quinones
Quinones are aromatic compounds characterized by a six-membered ring with two ketone substitutions. These compounds play critical roles in biological processes, such as electron transport, and are used in the synthesis of dyes, pharmaceuticals, and agrochemicals. Quinones exhibit unique redox properties, making them valuable in various applications. At CymitQuimica, we provide a wide range of high-quality quinones to support your research and industrial projects.
Products of "Quinones"
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α-Tocopherolquinone
CAS:Formula:C29H50O3Purity:95%~99%Color and Shape:Yellow oilMolecular weight:446.716Rhein-8-glucoside
CAS:Rhein-8-glucoside is a naturally occurring anthraquinone glycoside, which is derived primarily from the roots of plants such as Rheum species. These plants have been traditionally used in herbal medicine, and the glycoside form of Rhein enhances its solubility and bioavailability. The mode of action of Rhein-8-glucoside involves the modulation of various cellular pathways, including the inhibition of specific enzymes and the interaction with cellular receptors, potentially leading to anti-inflammatory, antioxidant, and antimicrobial effects. The uses and applications of Rhein-8-glucoside are predominantly in scientific research, where it is utilized to explore its pharmacological potential and understand its role in various biological processes. Researchers investigate its efficacy and mechanisms in the context of disease models, aiming to discover new therapeutic insights or adjunctive treatment strategies. Its study is particularly relevant in the fields of pharmacology and medicinal chemistry, where scientists are interested in its molecular interactions and potential health benefits. As research progresses, Rhein-8-glucoside continues to be an intriguing compound for ongoing investigation in natural product chemistry and drug discovery.Formula:C21H18O11Purity:Min. 95%Color and Shape:PowderMolecular weight:446.36 g/molAlizarin
CAS:QuinoneFormula:C14H8O4Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:240.22Tanshinone iia
CAS:Oxygen-heterocyclic compoundFormula:C19H18O3Purity:≥ 90.0 % (HPLC)Color and Shape:PowderMolecular weight:294.35Tetrafluoro-1,4-benzoquinone
CAS:Formula:C6F4O2Purity:>98.0%(T)(HPLC)Color and Shape:Light yellow to Brown powder to crystalMolecular weight:180.063-Geranyloxy-6-methyl-1,8-dihydroxyanthraquinone
3-Geranyloxy-6-methyl-1,8-dihydroxyanthraquinone is a natural anthraquinone compound, which is derived from certain plant species, notably those in the families Rubiaceae and Fabaceae. These compounds are often isolated through sophisticated extraction techniques that target bioactive substances present in botanical sources. The mode of action of 3-Geranyloxy-6-methyl-1,8-dihydroxyanthraquinone involves interactions at the cellular level, potentially regulating pathways critical for anti-inflammatory, antimicrobial, and anticancer activities. This is facilitated through its ability to interfere with enzymatic processes and modulate the expression of specific proteins or genes involved in disease progression. In terms of uses and applications, 3-Geranyloxy-6-methyl-1,8-dihydroxyanthraquinone is primarily investigated within the fields of pharmacology and medicinal chemistry. Its potential to serve as a lead compound in drug development projects centered around chronic diseases makes it a subject of significant scientific interest. Researchers are actively exploring its efficacy and safety through in vitro and in vivo studies, aiming to fully elucidate its therapeutic potential and develop novel interventions based on its chemical framework.Purity:Min. 95%2,3,5,6-Tetraaminocyclohexa-2,5-diene-1,4-dione
CAS:Formula:C6H8N4O2Purity:>95.0%(T)Color and Shape:Blue to Dark purple to Dark blue powder to crystalMolecular weight:168.16Embelin
CAS:Formula:C17H26O4Purity:>95.0%(T)(HPLC)Color and Shape:Light yellow to Yellow to Orange powder to crystalMolecular weight:294.392,5-Cyclohexadiene-1,4-dione, 2,5-dimethyl-
CAS:Formula:C8H8O2Purity:98%Color and Shape:SolidMolecular weight:136.147922,3,5-Trimethylcyclohexa-2,5-diene-1,4-dione
CAS:Formula:C9H10O2Purity:>98.0%(GC)Color and Shape:Light yellow to Yellow to Orange powder to crystalMolecular weight:150.18Protohypericin
CAS:Protohypericin is a photosensitizer, which is a compound known for its ability to absorb light and induce a photodynamic response. This compound is derived from the plant Hypericum perforatum, commonly known as St. John's Wort. The primary mode of action of protohypericin involves the absorption of specific wavelengths of light, leading to the generation of reactive oxygen species (ROS). These ROS are capable of inducing cell death, primarily through mechanisms such as apoptosis and necrosis. The applications of protohypericin are significant in the field of photodynamic therapy (PDT), an area of research that investigates the treatment of various cancers and bacterial infections using light-activated compounds. When exposed to light, protohypericin activates and targets malignant or pathogenic cells, making it a powerful tool in the treatment of tumors and microbial infections. Its natural origin and unique ability to induce photochemical responses make protohypericin a subject of intense study in therapeutic research, with ongoing investigations into optimizing its efficacy and broadening its range of applications.Formula:C30H18O8Purity:Min. 95%Color and Shape:PowderMolecular weight:506.46 g/molHarunganin
CAS:Harunganin is a natural compound, classified as a non-alkaloidal phloroglucinol derivative, which is derived from the plant Harungana madagascariensis, commonly found in tropical Africa. As a bioactive compound, Harunganin exhibits a mode of action that includes anti-inflammatory and antimicrobial effects. It achieves these effects by inhibiting the production of pro-inflammatory cytokines and modulating immune responses, as well as disrupting microbial cell wall synthesis. The primary application of Harunganin is in pharmacological research, where it is explored for its potential in developing therapies for inflammatory diseases, such as arthritis and skin conditions. Additionally, its antimicrobial properties make it a subject of interest for developing treatments against bacterial infections. Harunganin is also studied within ethnopharmacology for its traditional uses in herbal medicine, where it is employed for its purported benefits in treating various ailments, further informing its potential therapeutic applications.Formula:C30H36O4Purity:Mi. 90%Color and Shape:PowderMolecular weight:460.6 g/molChloranilic Acid
CAS:Formula:C6H2Cl2O4Purity:>98.0%(T)(HPLC)Color and Shape:Orange to Brown powder to crystalMolecular weight:208.98Aloin a
CAS:Natural glycosideFormula:C21H22O9Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:418.4