CAS 478-43-3
:Rhein
Description:
Rhein, with the CAS number 478-43-3, is a naturally occurring anthraquinone compound primarily found in various plants, particularly in the rhubarb species. It is characterized by its yellow crystalline appearance and is known for its potential medicinal properties, including anti-inflammatory, antioxidant, and laxative effects. Rhein exhibits solubility in organic solvents such as ethanol and dimethyl sulfoxide, but it is less soluble in water. The compound has garnered interest in pharmacological research due to its ability to modulate various biological pathways, including those involved in cell signaling and apoptosis. Additionally, Rhein has been studied for its potential applications in treating conditions such as diabetes and certain types of cancer. Its chemical structure features multiple hydroxyl groups, contributing to its reactivity and biological activity. As with many natural compounds, the safety and efficacy of Rhein in therapeutic contexts require further investigation through clinical studies.
Formula:C15H8O6
InChI:InChI=1S/C15H8O6/c16-9-3-1-2-7-11(9)14(19)12-8(13(7)18)4-6(15(20)21)5-10(12)17/h1-5,16-17H,(H,20,21)
InChI key:InChIKey=FCDLCPWAQCPTKC-UHFFFAOYSA-N
SMILES:O=C1C=2C(C(=O)C=3C1=C(O)C=CC3)=CC(C(O)=O)=CC2O
Synonyms:- 1,8-Dihydroxy-3-Carboxy anthraquinone
- 1,8-Dihydroxy-3-carboxyanthraquinone
- 1,8-Dihydroxyanthraquinone-3-carboxylic acid
- 2-Anthracenecarboxylic acid, 9,10-dihydro-4,5-dihydroxy-9,10-dioxo-
- 2-Anthraquinonecarboxylic acid, 4,5-dihydroxy-
- 2-Anthroic acid, 9,10-dihydro-4,5-dihydroxy-9,10-dioxo-
- 4,5-Dihydroxy-2-anthraquinonecarboxylic acid
- 4,5-Dihydroxy-9,10-Dioxo-9,10-Dihydroanthracene-2-Carboxylate
- 4,5-Dihydroxy-9,10-Dioxo-9,10-Dihydroanthracene-2-Carboxylic Acid
- 9,10-Dihydro-4,5-dihydroxy-9,10-dioxo-2-anthracenecarboxylic acid
- Cassic acid
- Chrysazin-3-carboxylic acid
- Monorhein
- NSC 38629
- Rheic acid
- Rheinic acid
- See more synonyms
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Found 18 products.
4,5-Dihydroxyanthraquinone-2-carboxylic Acid
CAS:Formula:C15H8O6Purity:>95.0%(T)(HPLC)Color and Shape:Light yellow to Brown powder to crystalMolecular weight:284.22Rhein, 97%
CAS:<p>Rhein is used to inhibit growth factor beta-1 induced plasminogen activator inhibitor-1 in endothelial cells. It acts as an antibacterial agent against Staphylococcus aureus. It is also used as a laxative. Further, it is employed as a pharmaceutical intermediate. This Thermo Scientific Chemicals bra</p>Formula:C15H8O6Purity:97%Molecular weight:284.22Rhein
CAS:Rhein analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C15H8O6Purity:(HPLC) ≥99%Color and Shape:PowderMolecular weight:284.23Rhein
CAS:<p>Rhein (NSC 38629) is an anthraquinone compound extracted from Polygonaceae Rheum Officinale with anti-inflammation and antitumor activities.</p>Formula:C15H8O6Purity:99.04%Color and Shape:Physical Description Yellow Needles (From Methanol) Or Yellow-Brown Powder (Ntp 1992)Molecular weight:284.221,8-DIHYDROXY-3-CARBOXYANTHRAQUINONE
CAS:Formula:C15H8O6Purity:98%Color and Shape:SolidMolecular weight:284.2204Rhein
CAS:Formula:C15H8O6Purity:≥ 98.0%Color and Shape:Yellow to orange powderMolecular weight:284.22Rhein
CAS:Rhein, an anthraquinone compound isolated from rhubarb, has been proved effective in treatment of experimental diabetic nephropathy (DN), one of the mechanism is the Inhibition of the hexosamine pathway.Formula:C15H8O6Purity:95%~99%Color and Shape:PowderMolecular weight:284.223Rhein
CAS:<p>Impurity Diacerein Impurity C<br>Stability Hygroscopic<br>Applications Found in the free state and as glucoside in Rheum spp, Polygonaceae (rhubarb) and in Senna leaves.A potential antioxidant resource: endophytic fungi from medicinal plants . Diacerein Impurity C<br>References Wanitschke, Pharmacology, 20, Suppl. 1, 21 (1980), Raimondi, L., et al.: Pharmacol. Res. Commun., 14, 103 (1982), Franchi-Micheli, S., et al.: J. Pharm. Pharmacol., 35, 262 (1983),<br></p>Formula:C15H8O6Color and Shape:NeatMolecular weight:284.22Rhein
CAS:<p>Rhein is an anthraquinone compound, which is derived from the plant rhubarb (Rheum species) with a range of unique biological activities. It functions primarily by inhibiting the activity of various enzymes and pathways involved in inflammation, oxidative stress, and cellular proliferation. Rhein is known for its ability to modulate the production of cytokines and other inflammatory mediators, offering potential therapeutic benefits in the treatment of inflammatory diseases.</p>Formula:C15H8O6Purity:Min. 98.0 Area-%Color and Shape:PowderMolecular weight:284.22 g/mol1,8-Dihydroxy-3-carboxyanthraquinone
CAS:Formula:C15H8O6Purity:98%Color and Shape:SolidMolecular weight:284.223















