ChemicalBook > CAS DataBase List > Diosmetin

Diosmetin

Product Name
Diosmetin
CAS No.
520-34-3
Chemical Name
Diosmetin
Synonyms
Diosmetine;Diosmetin (1.0 mg/mL in Methanol);5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-benzopyrone;Pillon;iosmetin;DIOSMETIN;Diosmetol;DIOSMETIN(P);Diosmetin-RM;Xiangye Lignin
CBNumber
CB2380858
Molecular Formula
C16H12O6
Formula Weight
300.26
MOL File
520-34-3.mol
More
Less

Diosmetin Property

Melting point:
256-258°C
Boiling point:
576.7±50.0 °C(Predicted)
Density 
1.512±0.06 g/cm3(Predicted)
vapor pressure 
0Pa at 20℃
storage temp. 
Sealed in dry,2-8°C
solubility 
Soluble in acetonitrile, DMSO (60 mg/ml), and ethanol (17 mg/ml), clear, light yellow to yellow.
form 
Solid
pka
6.50±0.40(Predicted)
color 
light yellow to yellow
Water Solubility 
19μg/L at 20℃
BRN 
294492
Stability:
Hygroscopic
InChIKey
MBNGWHIJMBWFHU-UHFFFAOYSA-N
LogP
3.1 at 20℃
CAS DataBase Reference
520-34-3(CAS DataBase Reference)
More
Less

Safety

Hazard Codes 
Xi,Xn
Risk Statements 
22
Safety Statements 
24/25
WGK Germany 
3
HS Code 
29329990
Hazardous Substances Data
520-34-3(Hazardous Substances Data)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
D7321
Product name
Diosmetin
Purity
≥98% (HPLC)
Packaging
10mg
Price
$98.4
Updated
2024/03/01
Sigma-Aldrich
Product number
PHL82526
Product name
Diosmetin
Purity
phyproof? Reference Substance
Packaging
25MG
Price
$298
Updated
2023/06/20
Sigma-Aldrich
Product number
90985
Product name
Diosmetin
Purity
analytical standard
Packaging
10mg
Price
$273
Updated
2022/05/15
Cayman Chemical
Product number
18649
Product name
Diosmetin
Purity
≥98%
Packaging
1g
Price
$180
Updated
2024/03/01
Cayman Chemical
Product number
18649
Product name
Diosmetin
Purity
≥98%
Packaging
5g
Price
$655
Updated
2024/03/01
More
Less

Diosmetin Chemical Properties,Usage,Production

Chemical Properties

Diosmetin is a flavonoid compound that appears as a yellow powder. It is extracted from lemon and also found in various other natural plants, including spearmint and spider incense. Diosmetin is slightly soluble in methanol but readily dissolves in DMSO.

Uses

Diosmetin (Diosmin EP Impurity F) is a metabolite of Apigenin. It exhibits anticancer, antimicrobial, antioxidant, oestrogenic, and anti-inflamatory activities. Diosmetin can be used in the production of functional foods, cosmetics, and future drugs with antioxidant, anti-infective and anti-shock effects.

Definition

ChEBI: Diosmetin is a monomethoxyflavone that is the 4'-methyl ether derivative of luteolin. It is a natural product isolated from citrus fruits which exhibits a range of pharmacological activities. It has a role as an antioxidant, an antineoplastic agent, a plant metabolite, a tropomyosin-related kinase B receptor agonist, an apoptosis inducer, an angiogenesis inhibitor, a cardioprotective agent, a bone density conservation agent, an anti-inflammatory agent and a vasodilator agent. It is a monomethoxyflavone, a trihydroxyflavone and a 3'-hydroxyflavonoid. It is functionally related to a luteolin. It is a conjugate acid of a diosmetin-7-olate.

Flammability and Explosibility

Not classified

Biological Activity

diosmetin (dio) is an agonist of the aryl hydrocarbon receptor (ahr). it potently inhibited the enzyme activity of cytochrome p450 1a1 (cyp1a1) in a dose-dependent manner with an ic50 value of approximately 30 nm, in microsomes from mcf-7 cells [1].ahr belongs to the per, arnt, sim/basic-helix-loop-helix superfamily of ligand-activated transcription factors. ahr mediates the toxic effects of polycyclic aromatic hydrocarbons, 2,3,7,8-tetrachlorodibenzo-p-dioxin (tcdd) and polychlorinated biphenyls. these chemicals all bind to ahr, and result in the activation of a battery of genes, including the cytochromes p450 cyp1a1, cyp1a2, and cyp1b1 [2].in mcf-7 cells, at 24 h after the incubation of diosmetin, cyp1a1 mrna was increased in a dose-dependent manner. in mcf-7 cells, diosmetin at 2.5 μm modestly increased cyp1a1 enzyme activity, with an activity increase in cells, while diosmetin at 5 μm did not increase the enzyme activity compared to controls in cells. compared with controls, diosmetin dose-dependently increased the capacity of nuclear extracts to bind an oligonucleotide containing the ahr-binding sequence of cyp1a1 [1].in the presence of cyp1a inhibitor, the concentration of diosmetin ranged from 25 μm at 0 h to 22 μm. in the absence of cyp1a inhibitor, the concentration of diosmetin ranged from 25 μm at 0 h to 15 μm [3].no in vivo result from the administration of diosmetin had been found.

References

[1]. ciolino hp, wang tt and yeh gc. diosmin and diosmetin are agonists of the aryl hydrocarbon receptor that differentially affect cytochrome p450 1a1 activity. cancer res, 1998, 58(13):2754-60. PMID: 9661887
[2]. gonzalez fj and fernandez-salguero p. the aryl hydrocarbon rreceptor studies using the ahr-null mice. drug metabolism and disposition, 1998, 26(12): 1194-1198. PMID: 9860927
[3]. and routsopoulos vp and spandidos da. The flavonoids diosmetin and luteolin exert synergistic cytostatic effects in human hepatoma HepG2 cells via CYP1A-catalyzed metabolism, activation of JNK and ERK and P53/P21 up-regulation. j nutr biochem, 2013, 24(2):496-504. DOI:10.1016/j.jnutbio.2012.01.012

Diosmetin Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Diosmetin Suppliers

MedChemexpress LLC
Tel
021-58955995
Fax
609-228-5909
Email
sales@medchemexpress.cn
Country
United States
ProdList
4861
Advantage
58
AdooQ BioScience, LLC
Tel
+1 (866) 930-6790
Fax
+1 (866) 333-9607
Email
info@adooq.com
Country
United States
ProdList
2782
Advantage
58
EMMX Biotechnology LLC
Tel
888-539-0666
Fax
888-539-0666
Email
info@emmx.com
Country
United States
ProdList
8447
Advantage
60
Target molecule Corp.
Tel
857-239-0968
Fax
857-239-8801
Email
service1@targetmol.com
Country
United States
ProdList
2559
Advantage
60
Musechem
Tel
+1-800-259-7612
Fax
+1-800-259-7612
Email
info@musechem.com
Country
United States
ProdList
4660
Advantage
60
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32161
Advantage
58
InvivoChem
Tel
+1-708-310-1919 +1-13798911105
Fax
708-557-7486
Email
sales@invivochem.cn
Country
United States
ProdList
6391
Advantage
58
BOC Sciences
Tel
+1-631-485-4226
Fax
1-631-614-7828
Email
inquiry@bocsci.com
Country
United States
ProdList
19553
Advantage
58
Cato Research Chemicals Inc.
Tel
020-81215950 4000-868-328
Email
customer@uwalab.com
Country
United States
ProdList
10404
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Protheragen-ING
Tel
+16313385890
Email
info@protheragen-ing.com
Country
United States
ProdList
3868
Advantage
58
ApexBio Technology
Tel
--
Fax
--
Email
sales@apexbt.com
Country
United States
ProdList
6251
Advantage
58
BOC Sciences
Tel
16314854226
Email
info@bocsci.com
Country
United States
ProdList
9923
Advantage
65
Cayman Chemical Company
Tel
--
Fax
--
Email
cayman@caymanchem.com
Country
United States
ProdList
6213
Advantage
81
MedChemExpress
Tel
--
Fax
--
Email
sales@medchemexpress.com
Country
United States
ProdList
6398
Advantage
58
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
Frontier Scientific, Inc.
Tel
--
Fax
--
Email
sales@frontiersci.com
Country
United States
ProdList
6222
Advantage
86
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
Alfa Chemistry
Tel
--
Fax
--
Email
info@Alfa-Chemistry.com
Country
United States
ProdList
6814
Advantage
0
SynFine Research
Tel
--
Fax
--
Email
research@synfine.com
Country
United States
ProdList
1024
Advantage
68
Wilshire Chemical Company Inc.
Tel
--
Fax
--
Email
WilshrChem@AOL.COM
Country
United States
ProdList
3498
Advantage
58
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6962
Advantage
56
Beta Pharma, Inc.
Tel
--
Fax
--
Email
sales@betapharma.com
Country
United States
ProdList
6226
Advantage
60
INDOFINE Chemical Company, Inc.
Tel
--
Fax
--
Email
chemical@indofinechemical.com
Country
United States
ProdList
6176
Advantage
69
2A PharmaChem USA
Tel
--
Fax
--
Email
sales@2apharmachem.com
Country
United States
ProdList
6137
Advantage
39
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
ChromaDex
Tel
--
Fax
--
Email
sales@chromadex.com
Country
United States
ProdList
2501
Advantage
76
LKT Laboratories, Inc.
Tel
--
Fax
--
Email
info@lktlabs.com
Country
United States
ProdList
2164
Advantage
64
More
Less

View Lastest Price from Diosmetin manufacturers

Hebei Zhuanglai Chemical Trading Co Ltd
Product
Diosmetin 520-34-3
Price
US $150.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
500kg
Release date
2024-12-11
Changzhou Xuanming Pharmaceutical Technology Co., Ltd.
Product
Diosmetin 520-34-3
Price
US $30.00-110.00/G
Min. Order
1G
Purity
99
Supply Ability
1000
Release date
2024-10-28
BINBO BIOLOGICAL CO.,LTD
Product
Diosmetin 520-34-3
Price
US $0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1000 kg
Release date
2024-04-24

520-34-3, DiosmetinRelated Search:


  • 3',5,7-TRIHYDROXY-4'METHOXYFLAVONE
  • 4'-METHOXY-5,7,3'-TRIHYDROXYFLAVONE
  • 4-METHOXY-5,7,3'-TRIHYDROXYFLAVONE
  • 5,7,3'-TRIHYDROXY-4'-METHOXYFLAVONE
  • DIOSMETIN
  • 5,7-Dihydroxy-2-[3-hydroxy-4-methoxyphenyl]-[4H]-1-benzopyran-4-one
  • 4'-Methylluteolin
  • Diosmetine
  • Diosmetol
  • Luteolin 4'-Methyl Ether
  • Pillon
  • DIOSMETIN(P)
  • DIOSMETIN WITH HPLC
  • 5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-benzopyrone
  • 2-(3-Hydroxy-4-methoxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one
  • DiosMetin(Luteolin 4-Methyl ether)
  • Salinigricoflavonol
  • 5,7-dihydroxy-2-(3-hydroxy-4-Methoxyphenyl)-4H-chroMen-4-one
  • DiosMetin, froM DendrantheMaMorifoliuM
  • 4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-
  • ,5,7-Trihydroxy-4′-methoxyflavone
  • 5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one
  • Diosmetin, 98%, from Dendranthemamorifolium
  • Diosmin Impurity 6 (Diosmin EP Impurity F)(Diosmetin)
  • Diosmetin 520-34-3
  • Diosmin EP Impurity F(Diosmetin)
  • Diosmin EP Impurity F
  • Diosmetin (Diosmin EP Impurity F)
  • iosmetin
  • Diosmetin (1.0 mg/mL in Methanol)
  • Diosmetin/ Diosmetin
  • Diosmetin, 97%+
  • Diosmin Aglycone
  • 5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one (diosmetin),
  • Diosmetin (Diosmin Impurity F)
  • Xiangye Lignin
  • Diosmetin-RM
  • Dioxamine EP Impurity F
  • Diosmin Impurity F
  • 520-34-3
  • C16H12O6
  • Inhibitors
  • CITRIMORE
  • Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals
  • reagent
  • Tetra-substituted Flavones
  • Intermediates & Fine Chemicals
  • Metabolites & Impurities
  • Pharmaceuticals