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Factory Supply High Grade 480-41-1 with the Best Price Naringenin

Factory Supply High Grade 480-41-1 with the Best Price Naringenin CAS NO.480-41-1

  • FOB Price: USD: 200.00-200.00 /Kilogram Get Latest Price
  • Min.Order: 1 Kilogram
  • Payment Terms: L/C,D/A,D/P,T/T,
  • Available Specifications:

    99%(1.0000-5.0000)Kilogram

  • Product Details

Keywords

  • Naringenin factory
  • Naringenin high purity
  • 480-41-1

Quick Details

  • ProName: Naringenin 480-41-1 high purity fact...
  • CasNo: 480-41-1
  • Molecular Formula: C15H12O5
  • Appearance: Solid powder
  • Application: Applied in dietary supplements,pharmac...
  • DeliveryTime: Prompt after order confirmation
  • PackAge: Foil bag or drum
  • Port: Beijing or Guangzhou Port
  • ProductionCapacity: 5000 Kilogram/Day
  • Purity: 99% BY HPLC
  • Storage: Sealed,light and oxygen resistant
  • Transportation: by sea or air
  • LimitNum: 1 Kilogram
  • Grade: Industrial Grade,Food Grade,Pharma Gra...

Superiority

Naringenin 480-41-1

Naringenin is a natural predominant flavanone derived from plant food with antioxidant and anti-inflammatory activity. Naringenin reduces oxidative damage to DNA in vitro, and increases VLDL as well as cholesterol levels. Naringenin is used for the treatment of HCV infection. Naringenin can be used as nutritional supplement in health care products.

Naringenin is a weak estrogen that also exhibits partial antiestrogenic activity in the female rat uterus and MCF-7 human breast cancer cells. Naringenin is also a agent for the treatment of hepatitis C virus (HCV) infection. Naringenin has hypocholesterolemic, antioxidant, free radical scavenger, anti-cancer, anti-inflammatory, neuroprotective, carbohydrate metabolism promoter, and immune system modulator properties. Naringenin possesses potent antidepressant-like property via the central serotonergic and noradrenergic systems.

Details

(S)-naringenin is the (S)-enantiomer of naringenin. It has a role as an expectorant and a plant metabolite. It is a naringenin and a (2S)-flavan-4-one. It is a conjugate acid of a (S)-naringenin(1-). It is an enantiomer of a (R)-naringenin.

Naringenin is a flavonoid commonly found in grapefruits which functions as an antioxidant, free radical scavenger, anti-inflammatory compound, carbohydrate metabolism promoter, and immune system modulator. Studies indicate that in vitro Naringenin reduces oxidative damage to DNA. In addition, Naringenin potently inhibits the secretion of very-low-density lipoproteins by cells. Furthermore, Naringenin has been shown to reduce cholesterol concentrations in hepatocytes and plasma cells via inhibiting HMGCR (HMG-CoA reductase). Studies conducted on Hepatitis C virus particles demonstrate that Naringenin can inhibit the virus via a PPAR-mediated mechanism by inhibiting the long term assembly of the virus.

Factory Supply High Grade 480-41-1 with the Best Price

  • Molecular Formula:C15H12O5
  • Molecular Weight:272.257
  • Appearance/Colour:beige-brown powder 
  • Vapor Pressure:6.18E-14mmHg at 25°C 
  • Melting Point:247-250 °C 
  • Refractive Index:1.692 
  • Boiling Point:577.5°C at 760mmHg 
  • PKA:7.52±0.40(Predicted) 
  • Flash Point:224.7°C 
  • PSA:86.99000 
  • Density:1.485 g/cm3 
  • LogP:2.50990 

Naringenin(Cas 480-41-1) Usage

Pharmacological effects

Naringenin is the aglycone of naringin, it belongs to dihydro-flavonoids, at room temperature it is a white needle crystal(methanol), soluble in alcohol, ether and benzene, almost insoluble in water. In HCl-Mg powder reaction,it is cherry red ,in sodium borohydride reaction it is red purple, in molish reaction,it is negative. In the nature, it is mainly from the Rosaceae cherry (Prunus yedoensis Mate.) bud,and sumac plants (Amacardi-um occidentale L.)? fruits’ core-shell. Nucleus structure is similar among flavonoids, most of the components do not have ideal fat-soluble and water-soluble abilities, the bioavailability is low. By modifying its structure, the introduction of strongly fat-soluble or water-soluble groups can increase its fat-soluble or water-soluble abilities, thus improving the bioavailability. The structure modification includes alkylation, acylation, sulfonation,glycosidation? of hydroxyl groups and the formation of the metal complex. The effects of naringenin including: anti-bacterial, anti-inflammatory, antioxidant, cough expectorant,decreasing blood fat, anti-cancer and anti-tumor, antispasmodic, scavenging free radicals, prevention and treatment of liver disease, inhibition of platelet aggregation, anti-atherosclerosis and others , which can be widely used in medicine, food and other fields. 1. Antibacterial: it has a strong antibacterial effect on Staphylococcus aureus, Escherichia coli, Shigella dysenteriae, and Salmonella typhi. Naringenin also has effect on fungi? , 1000ppm is sprayed onto the rice, blast fungus infection can be reduced 40-90%,and it is not toxic to livestock and humans. 2. Anti-inflammatory: intraperitoneal injection of 20mg/kg per day for rats can inhibit the inflammatory process which caused by wool ball implantation. 3. Anticancer:? it displays action in L1210 leukemia and sarcomas in rats. 4. Antispasmodic and gallbladder: among the flavonoids,it has stronger effects. Naringenin has a strong effect on increasing bile secretion in experimental animals.

Application

It has anti-bacterial, anti-inflammatory, anti-cancer, antispasmodic and choleretic effects.

Purification Methods

Crystallise it from EtOH or aqueous EtOH. It has UV: at 290nm (EtOH). The S(-)-enantiomer (natural form) has m 255-256o (from EtOH) and [] D -28.0o (c 2, EtOH), [] D -35.2o (c 1, pyridine).

InChI:InChI=1/C15H12O5/c16-9-3-1-8(2-4-9)13-7-12(19)15-11(18)5-10(17)6-14(15)20-13/h1-6,13,16-18H,7H2/t13-/m1/s1

480-41-1 Relevant articles

Synthesis, structural elucidation and antiradical activity of a copper (II) naringenin complex

Celiz, Gustavo,Suarez, Sebastián A.,Arias, Analía,Molina, José,Brondino, Carlos D.,Doctorovich, Fabio

, p. 595 - 610 (2019)

Coupling the extraction and derivatizati...

Development and evaluation of an HPLC method for accurate determinations of enzyme activities of naringinase complex

Ni, Hui,Xiao, An-Feng,Wang, Ya Qi,Chen, Feng,Cai, Hui-Nong,Su, Wen-Jun

, p. 10026 - 10032 (2013)

An HPLC method that can separate naringi...

Sulfation of naringenin by Cunninghamella elegans

Ibrahim, Abdel-Rahim S.

, p. 209 - 212 (2000)

A new flavonoid sulfate, naringenin-7-su...

-

Zapesochnaya et al.

, (1972)

-

GLUCOSYLATED FLAVONOIDS AND OTHER PHENOLIC COMPOUNDS FROM SORGHUM

Gujer, Rene,Magnolato, Daniele,Self, Ron

, p. 1431 - 1436 (1986)

The principal tannin constituents of sor...

Design, synthesis, and cholinesterase inhibition assay of liquiritigenin derivatives as anti-Alzheimer's activity

Guan, Liping,Jia, Jinjing,Jiang, Haiying,Peng, Dingxin,Zhang, Li

, (2021/10/01)

The marine environment is a rich resourc...

Discovery of Novel Bacterial Chalcone Isomerases by a Sequence-Structure-Function-Evolution Strategy for Enzymatic Synthesis of (S)-Flavanones

Bornscheuer, Uwe T.,Brückner, Stephan I.,Gei?ler, Torsten,Gross, Egon,Hartmann, Beate,Ley, Jakob P.,Meinert, Hannes,R?ttger, Carsten,Schuiten, Eva,Yi, Dong,Zirpel, Bastian

supporting information, p. 16874 - 16879 (2021/07/06)

Chalcone isomerase (CHI) is a key enzyme...

Flavanone compound as well as preparation method and application thereof

-

Paragraph 0202-0205, (2021/04/17)

The invention belongs to the technical f...

Novel chromenone derivatives having substituted biphenyl group and a pharmaceutical composition for prevention or treatment of allergic diseases compring the same

-

Paragraph 0157-0164; 0166-0170, (2020/11/26)

The present invention relates to: a nove...

480-41-1 Process route

(-)-(S)-sakuranetin
520-29-6,2957-21-3,17784-36-0,118244-13-6

(-)-(S)-sakuranetin

7-methoxy-3',4',5-trihydroxyflavanone
93012-86-3

7-methoxy-3',4',5-trihydroxyflavanone

eriodictyol
552-58-9

eriodictyol

7-methoxyflavanone
21785-09-1

7-methoxyflavanone

naringenin
480-41-1

naringenin

Conditions
Conditions Yield
With cytochromes P450 in human liver microsomes; Kinetics; Enzymatic reaction;
 
prunin
529-55-5,88275-21-2,127469-97-0

prunin

alpha-D-glucopyranose
492-62-6

alpha-D-glucopyranose

naringenin
480-41-1

naringenin

Conditions
Conditions Yield
With β-D-glucosidase; In aq. buffer; at 50 - 100 ℃; for 0.166667h; pH=5; Enzymatic reaction;
 

480-41-1 Upstream products

  • 529-41-9
    529-41-9

    (2S)-(-)-naringenin-5-O-β-D-glucopyranoside

  • 112294-87-8
    112294-87-8

    4,2',4',6'-tetrahydroxychalchone 4'-glucoside

  • 94392-49-1
    94392-49-1

    naringenin 7-O-(6-O-((E)-p-coumaroyl)-β-D-glucopyranoside)

  • 520-29-6
    520-29-6

    (-)-(S)-sakuranetin

480-41-1 Downstream products

  • 18196-13-9
    18196-13-9

    (S)-7-acetoxy-2-(4-acetoxy-phenyl)-5-hydroxy-chroman-4-one

  • 105393-75-7
    105393-75-7

    4',5,7-tris(trimethylsilyl)naringenin

  • 53846-50-7
    53846-50-7

    sophoraflavanone B

  • 119240-82-3
    119240-82-3

    3’-prenylnaringenin

Other products of this supplier

Kono Chem Co.,LtdTel:86-29-86107037-8015 Fax:86-29-81330164  Email:info@konochemical.com
 Address:No.11 Daqing Road,Lianhu District,Xi’an 710082,China,710082