B0189

Casticin

from Vitex trifolia, ≥98% (HPLC)

• Synonym(e): Casticine, Quercetagetin 3,6,7,4′-tetramethyl ether, Vitexicarpin
• Empirische Formel (Hill-System): C₁₉H₁₈O₈
• CAS-Nummer: 479-91-4
• Molekulargewicht: 374.34
• UNSPSC Code: 12352200
• NACRES: NA.25

Eigenschaften

• Produktname: Casticin, from Vitex trifolia, ≥98% (HPLC)
• InChI: 1S/C19H18O8/c1-23-11-6-5-9(7-10(11)20)17-19(26-4)16(22)14-12(27-17)8-13(24-2)18(25-3)15(14)21/h5-8,20-21H,1-4H3
• InChI key: PJQLSMYMOKWUJG-UHFFFAOYSA-N
• biological source: Vitex trifolia
• assay: ≥98% (HPLC)
• form: powder
• solubility: ethanol: 1 mg/mL, clear, colorless to light yellow
• application(s): metabolomics; vitamins, nutraceuticals, and natural products
• storage temp.: 2-8°C

Beschreibung

Application

Casticin from Vitex trifolia is used to study its mechanisms of action as an antiiflammatory and anticancer agent via processes such as TRAIL-induced apoptosis, cell cycle arrest, ROS generation, and glutathione (GSH) depletion.

Biochem/physiol Actions

Casticin has anticancer, pro-apoptotic, anti-proliferative, anti-asthmatic, and anti-angiogenic properties. In addition, it exhibits anti-inflammatory behavior by means of its inhibitory effect on lipoxygenases and T- & B-lymphocytes. Due to its oestrogenic activity, it is being used to manage Premenstrual syndrome in women. It is also reported to mitigate rheumatoid arthritis and liver fibrosis manifestations.[1]

Tubulin-binding anticancer flavonoid. Casticin induces apoptosis in cancer cells.

General description

Casticin is one of the flavonoids present in the traditional Chinese medicine Inula japonica Thunb.[2] It is a polymethyl compound with three rings, a catechol moiety at ortho position, one double bond, two hydroxyl groups, and four methoxy groups. It has been isolated from the fruits, seeds, and leaves of various Vitex species.[1]

Sicherheitshinweise

• Lagerklasse: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable