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Fisetine

Basic information

  • Product Name:Fisetine
  • CasNo.:528-48-3
  • MF:C15H10O6
  • MW:286.241

Physical and Chemical Properties

  • Purity:99%
  • Boiling Point:330 ºC
  • Packing:yellow to brown crystalline powder
  • Throughput:
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Product Details

CasNo: 528-48-3

MF: C15H10O6

Appearance: yellow to brown crystalline powder

Cost-effective and customizable Fisetine 528-48-3 factory

  • Molecular Formula:C15H10O6
  • Molecular Weight:286.241
  • Appearance/Colour:yellow to brown crystalline powder 
  • Vapor Pressure:3.23E-15mmHg at 25°C 
  • Melting Point:330 ºC 
  • Refractive Index:1.784 
  • Boiling Point:599.4 ºC at 760 mmHg 
  • PKA:6.83±0.40(Predicted) 
  • Flash Point:233 ºC 
  • PSA:111.13000 
  • Density:1.688 g/cm3 
  • LogP:2.28240 

Fisetin(Cas 528-48-3) Usage

Anticancer Research

Fisetin is a plant polyphenol from the flavonoid group. It occurs in fruits and vegetablesincluding persimmons, strawberries, onions, cucumbers, and apples. It is anantioxidant, exerts anticarcinogenic effects in HCT-116 (human colon carcinoma)cells, and modulates protein kinase and lipid kinase pathways (Wang et al. 2012).Fisetin alter signaling pathway like MAPK, NF-κB, activators of transcription(JAK/STAT), Janus kinase/signal transducers, phosphoinositide-3-kinase-proteinkinase (PI3K/Akt), Wnt, and mammalian target of rapamycin (mTOR), therebyleading to cell cycle arrest in HL-60 cells (human acute promyelocytic leukemiacells) (Singh et al. 2016b). Thus, it exhibits inhibitory effects on adhesion, migration,invasion, and multidrug resistance (Suh et al. 2009).

General Description

This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG

InChI:InChI=1/C15H10O6/c16-8-2-3-9-12(6-8)21-15(14(20)13(9)19)7-1-4-10(17)11(18)5-7/h1-6,16-18,20H

528-48-3 Relevant articles

A synthesis method of fisetin

-

, (2019/04/10)

The invention provides a method for synt...

Synthesis of fisetin and 2′,4′,6′-trihydroxydihyrochalcone 4′-O-β-neohesperidoside based on site-selective deacetylation and deoxygenation

Tsunekawa, Ryuji,Hanaya, Kengo,Higashibayashi, Shuhei,Sugai, Takeshi

, p. 1316 - 1322 (2018/07/29)

Fisetin and 2′,4′,6′-trihydroxydihyrocha...

Profiling of flavonol derivatives for the development of antitrypanosomatidic drugs

Borsari, Chiara,Lucian, Rosaria,Pozzi, Cecilia,Poehner, Ina,Henrich, Stefan,Trande, Matteo,Cordeiro-Da-silva, Anabela,Santarem, Nuno,Baptista, Catarina,Tait, Annalisa,Di Pisa, Flavio,Iacono, Lucia Dello,Landi, Giacomo,Gul, Sheraz,Wolf, Markus,Kuzikov, Maria,Ellinger, Bernhard,Reinshagen, Jeanette,Witt, Gesa,Gribbon, Philip,Kohler, Manfred,Keminer, Oliver,Behrens, Birte,Costantino, Luca,Nevado, Paloma Tejera,Bifeld, Eugenia,Eick, Julia,Clos, Joachim,Torrado, Juan,Jiménez-Antón, María D.,Corral, María J.,Alunda, José Ma,Pellati, Federica,Wade, Rebecca C.,Ferrari, Stefania,Mangani, Stefano,Costi, Maria Paola

, p. 7598 - 7616 (2016/09/04)

Flavonoids represent a potential source ...

MICROBIAL PRODUCTION OF THE FLAVONOIDS GARBANZOL, RESOKAEMPFEROL AND FISETIN

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Page/Page column 51; 52, (2016/06/01)

The invention provides a genetically mod...

528-48-3 Process route

3,4,2',4'-tetrahydroxy-chalcone
487-52-5,21849-70-7

3,4,2',4'-tetrahydroxy-chalcone

3,7,3',4'-tetrahydroxyflavone
528-48-3

3,7,3',4'-tetrahydroxyflavone

Conditions
Conditions Yield
With sodium carbonate / sodium bicarbonate buffer solution; potassium hydrogen sulfate complex; In dichloromethane; acetone; at 20 ℃; for 21h;
96.7%
3,3′,4′,7-tetraacetoxyflavone
114840-33-4

3,3′,4′,7-tetraacetoxyflavone

3,7,3',4'-tetrahydroxyflavone
528-48-3

3,7,3',4'-tetrahydroxyflavone

Conditions
Conditions Yield
With sodium dithionite; water; sodium hydroxide; In methanol; at 20 ℃; for 4h; Inert atmosphere;
65%

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528-48-3 Downstream products

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    17093-86-6

    3,3',4',7-tetra-O-methylfisetin

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    114840-33-4

    3,3′,4′,7-tetraacetoxyflavone

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    99-50-3

    3,4-Dihydroxybenzoic acid

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    4-hydroxysalicylic acid