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经验公式(希尔记法):
C15H10O5
化学文摘社编号:
分子量:
270.24
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
1291621
MDL number:
NACRES:
NA.21
Assay:
≥95%
Form:
powder or crystals
Solubility:
DMF: soluble, DMSO: soluble, methanol: soluble
InChI key
GYLUFQJZYAJQDI-UHFFFAOYSA-N
SMILES string
C1=CC(=CC=C1C2=COC3=CC(=C(C=C3C2=O)O)O)O
InChI
InChI=1S/C15H10O5/c16-9-3-1-8(2-4-9)11-7-20-14-6-13(18)12(17)5-10(14)15(11)19/h1-7,16-18H
biological source
synthetic
assay
≥95%
form
powder or crystals
color
, Faint Yellow to Yellow to Brown
mp
320 °C
solubility
DMF: soluble, DMSO: soluble, methanol: soluble
application(s)
clinical research
general analytical
life science and biopharma
metabolomics
shipped in
2-8°C
storage temp.
−20°C
Quality Level
General description
6-Hydroxydaidzein, also known as 4′,6,7-trihydroxyisoflavone, is a hydroxylated derivative of daidzein, distinguished by an additional hydroxyl group at the 6th position. It belongs to the class of organic compounds called isoflavones, which are polycyclic structures featuring a 2-isoflavene core and a ketone group at the C4 carbon. This composition classifies 6-hydroxydaidzein as a flavonoid.
This compound has been detected in foods such as soybeans (Glycine max) and various pulses, suggesting its potential as a biomarker for the consumption of these plant-based products. As a primary metabolite, 6-hydroxydaidzein plays a vital role in an organism′s growth, development, and reproduction. Numerous studies have highlighted its pharmacological properties, including tyrosinase inhibition, anti-cancer activity, anti-obesity effects, and cognitive enhancement.
Current research has demonstrated that 6-hydroxydaidzein may inhibit enzyme activities and critical signaling pathways, although this effect may be reversed by coumarin derivatives. Research utilizing in vitro assays and molecular docking has also investigated its potential impact on antibiotic-resistant bacterial strains. Functionally, 6-hydroxydaidzein serves multiple roles, including acting as a PPARalpha and PPARgamma agonist, an anti-inflammatory agent, an antimutagen, and a tyrosinase inhibitor.
This compound has been detected in foods such as soybeans (Glycine max) and various pulses, suggesting its potential as a biomarker for the consumption of these plant-based products. As a primary metabolite, 6-hydroxydaidzein plays a vital role in an organism′s growth, development, and reproduction. Numerous studies have highlighted its pharmacological properties, including tyrosinase inhibition, anti-cancer activity, anti-obesity effects, and cognitive enhancement.
Current research has demonstrated that 6-hydroxydaidzein may inhibit enzyme activities and critical signaling pathways, although this effect may be reversed by coumarin derivatives. Research utilizing in vitro assays and molecular docking has also investigated its potential impact on antibiotic-resistant bacterial strains. Functionally, 6-hydroxydaidzein serves multiple roles, including acting as a PPARalpha and PPARgamma agonist, an anti-inflammatory agent, an antimutagen, and a tyrosinase inhibitor.
Application
6-hydroxydaidzein finds application in metabolomics, biochemical and life science related research.
Features and Benefits
Versatile and adaptable for wide variety of research and metabolomics applications.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
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