Anthraquinones and derivatives
Anthraquinones have a structure based on a benzene core fused with a quinone ring. This structure grants them high stability and reactivity with a variety of biomolecules. Anthraquinone derivatives can be used for their biological properties, including antibacterial, anti-inflammatory, and laxative activities, as well as potential applications in the synthesis of pharmaceutical compounds and the chemical industry.
At CymitQuimica, we offer anthraquinones and their derivatives with various applications in organic and pharmaceutical chemistry.
Found 405 products of "Anthraquinones and derivatives"
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9,10-dioxo-9,10-dihydroanthracene-2-carbonyl chloride
CAS:Purity:98.0%Molecular weight:270.67001342773441-(Methylamino)-4-(phenylamino)anthracene-9,10-dione
CAS:Purity:95.0%Molecular weight:328.37100219726561,4-Bis((4-butylphenyl)amino)-5,8-dihydroxyanthracene-9,10-dione
CAS:Purity:98%Molecular weight:534.6560058593759,10-Dioxo-9,10-dihydroanthracene-2-sulfonyl chloride
CAS:Purity:97%Molecular weight:306.7200012207031Ref: 10-F801706
1gTo inquire5gTo inquire10mgTo inquire25mgTo inquire50mgTo inquire100mgTo inquire250mgTo inquireBisoxatin
CAS:<p>Bisoxatin (LA 271A) is an oral laxative that can be used to study contact laxatives for chronic constipation.</p>Formula:C20H15NO4Purity:99.47%Color and Shape:SolidMolecular weight:333.34Daunorubicinol-13C,d3 (mixture of diastereomers)
CAS:Controlled Product<p>Applications A metabolite of Daunorubicin. Used as an antineoplastic. Complexes with DNA. Inhibits DNA and RNA synthesis.<br>References Mizuno, N.S., et al.: Cancer Res., 35, 1542 (1975), Munger, C., et al.: Cancer Res., 48, 2404 (1988), Kobayashi, Y., et al.: J. Biol. Chem., 275, 17639 ( 2000), Burke, B., et al.: Cardiovasc. Toxicol., 2, 41 (2002),<br></p>Formula:CC26D3H28NO10Color and Shape:NeatMolecular weight:533.55Sodium 1-amino-9,10-dioxo-9,10-dihydroanthracene-2-sulfonate
CAS:Purity:95%Molecular weight:325.26998901367191-amino-2-methylanthra-9,10-quinone
CAS:Purity:98.0%Color and Shape:Liquid, No data available.Molecular weight:237.25799560546875Doxorubicin impurity
CAS:<p>Doxorubicin is an organic compound that belongs to the class of polycyclic aromatic hydrocarbons. It is used as a cancer therapy, primarily in the treatment of breast cancer. The chemical sensing of impurities in doxorubicin can be done using phase transfer methods. The quantification of these impurities can be done using high-performance liquid chromatography (HPLC) or gas chromatography (GC).</p>Formula:C26H27NO11Purity:Min. 90 Area-%Color and Shape:Red PowderMolecular weight:529.49 g/molDaunomycinone
CAS:<p>Daunomycinone is a chemical compound that belongs to the group of antitumor agents. It is used in cancer therapy and has been shown to inhibit protein synthesis, leading to cell death. Daunomycinone can be synthesized by reacting adriamycin with trifluoroacetic acid in the presence of an organic base. This reaction produces a daunomycinone molecule that has a hydroxyl group at one end and a carbonyl group at the other. The binding constants between daunomycinone and human serum proteins have been determined experimentally using molecular modeling techniques. Hydrogen bonding interactions are also present in this complex, which may account for its high affinity for proteins found in human serum.</p>Formula:C21H18O8Purity:Min. 95%Color and Shape:Red PowderMolecular weight:398.36 g/molDaunorubicinol
CAS:<p>Daunorubicin metabolite</p>Formula:C27H31NO10Purity:Min. 95%Color and Shape:Red PowderMolecular weight:529.54 g/mol
