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Formononetin

≥99.0% (TLC)

Synonim(y):

7-Hydroxy-3-(4-methoxyphenyl)-4H-1-benzopyran-4-one, 7-Hydroxy-3-(4-methoxyphenyl)chromone, 7-Hydroxy-4′-methoxyisoflavone, Biochanin B, Daidzein 4′-methyl ether, Formonetin, Formononetol

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Gabaryty przesyłkiSKUDostępnośćCena netto
5 mg
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530,00 zł

Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C16H12O4
Numer CAS:
Masa cząsteczkowa:
268.26
UNSPSC Code:
12352200
NACRES:
NA.47
PubChem Substance ID:
EC Number:
207-623-9
Beilstein/REAXYS Number:
237979
MDL number:

530,00 zł


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Quality Segment

assay

≥99.0% (TLC)

form

solid

mp

257-261 °C

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

SMILES string

COc1ccc(cc1)C2=COc3cc(O)ccc3C2=O

InChI

1S/C16H12O4/c1-19-12-5-2-10(3-6-12)14-9-20-15-8-11(17)4-7-13(15)16(14)18/h2-9,17H,1H3

InChI key

HKQYGTCOTHHOMP-UHFFFAOYSA-N

General description

Formononetin is an O-methylated isoflavone[1], a phytoestrogen.[2] It can be found in many legumes, different species of clovers primarily in Trifolium pratense L. (red clovers), and one of the main flavonoids found in Astragalus membranaceus (Huangqi).[1]

Application

Formononetin has been used:
  • as a reference standard to study export of multiple metabolites from Crocus sativus stigma extracts using liquid chromatography-photodiode array-high resolution mass spectrometry (LC-PDA-HRMS)[3]
  • as phytoestrogen-mimetic isoflavones to test its antioxidant effects in a biomimetic environment using chemiluminescence method
  • as an authentic standard to test the isoflavones content level in both wild type and transgenic Medicago truncatula plant using high-performance liquid chromatography (HPLC)[4]
  • to test its effects as a potential Aryl hydrocarbon receptor (AhR)-agonist on the restoration of skin barrier proteins for Atopic dermatitis (AD) treatment using different keratinocyte cell lines and human skin equivalent (HSE) model[5]

Biochem/physiol Actions

Formononetin elicits antioxidant, anti-inflammatory, anti-hyperlipidemic, and cardioprotective effects.[6] It displays antidiabetic properties known to be effective against diabetic nephropathy in type 2 diabetes mellitus.[6] Formononetin is a well-known anti-cancer and chemotherapeutic agent that is used in cancer therapy.[1] It also displays antimicrobial, neuroprotective, and anti-hypertensive properties.[2]
Isoflavone found in red clover. Effective against Giardia lamblia infection, at least partially by inducing detachment of trophozoites from intestinal mucosa.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.
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Ta pozycja
34421594334PHL89528
Formononetin phyproof® Reference Substance

PHL89528

Formononetin

assay

≥99.0% (TLC)

assay

≥90% (HPLC)

assay

≥98.0% (HPLC)

assay

≥95.0% (HPLC)

form

solid

form

solid

form

-

form

-

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

-

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

application(s)

-

application(s)

food and beverages

application(s)

food and beverages

mp

257-261 °C

mp

-

mp

-

mp

-


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Klasa składowania

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Produkty

Antioxidants protect biological systems from oxidative damage produced by oxygen-containing free radicals and from redoxactive transition metal ions such as iron, copper, and cadmium.


Abdul Malik Tyagi et al.
Menopause (New York, N.Y.), 19(8), 856-863 (2012-07-12)
Formononetin (Formo) prevents ovariectomy (Ovx)-induced bone loss in rats. However, there are no reports on the curative effects of Formo. The objective of this study was to investigate the ability of Formo in restoring trabecular microarchitecture and promoting new bone
Kai-Ching Tay et al.
Frontiers in pharmacology, 10, 820-820 (2019-08-14)
Cancer, a complex yet common disease, is caused by uncontrolled cell division and abnormal cell growth due to a variety of gene mutations. Seeking effective treatments for cancer is a major research focus, as the incidence of cancer is on
Olivia Costantina Demurtas et al.
The Plant cell, 31(11), 2789-2804 (2019-09-25)
Compartmentation is a key strategy enacted by plants for the storage of specialized metabolites. The saffron spice owes its red color to crocins, a complex mixture of apocarotenoid glycosides that accumulate in intracellular vacuoles and reach up to 10% of



Numer pozycji handlu globalnego

SKUNUMER GTIN
47752-25MG-F04061832404431
47752-5MG-F04061832373089

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