419788
7-Methoxyflavanone
98%
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About This Item
Empirical Formula (Hill Notation):
C16H14O3
CAS Number:
Molecular Weight:
254.28
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
InChI
1S/C16H14O3/c1-18-12-7-8-13-14(17)10-15(19-16(13)9-12)11-5-3-2-4-6-11/h2-9,15H,10H2,1H3
SMILES string
COc1ccc2C(=O)CC(Oc2c1)c3ccccc3
InChI key
VYESEQLQFXUROZ-UHFFFAOYSA-N
assay
98%
mp
89-91 °C (lit.)
Gene Information
human ... CYP19A1(1588)
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Zhao Qu et al.
The Journal of pharmacy and pharmacology, 72(3), 385-395 (2019-12-24)
Neuroprotective potential of 7-methoxyflavanone (7MF) and its underlying mechanism was investigated. Inhibitory effects of 7MF on microglial activation and neuroinflammation were evaluated by employment of lipopolysaccharide (LPS)-induced BV2 microglial cells. Changes in expression of genes and proteins of interest were
Mariana Silva et al.
Journal of chromatography. A, 1490, 166-176 (2017-02-17)
In this paper a chiral stationary phase (CSP) was prepared by the immobilization of a β-CD derivative (3,5-dimethylphenylcarbamoylated β-CD) onto the surface of amino-functionalized spherical ordered mesoporous silica (denoted as SM) via a urea linkage using the Staudinger reaction. The
Giovanni D'Orazio et al.
Journal of chromatography. A, 1623, 461213-461213 (2020-06-09)
In the present study separation of enantiomers of some chiral neutral, basic and weakly acidic analytes was investigated on the chiral stationary phase (CSP) made by covalent immobilization of amylose tris(3-chloro-5-methylphenylcarbamate) onto aminopropylsilanized (APS) silica in nano-liquid chromatography (nano-LC) in
Karen J Marsh et al.
Phytochemistry, 160, 31-39 (2019-01-27)
A group of plant specialised metabolites (PSMs) collectively known as unsubstituted B-ring flavanones (UBFs) have previously been found in the foliage of some species from the genus Eucalyptus L'Hér. (Myrtaceae), specifically from the subgenus Eucalyptus (monocalypts). Captive feeding studies using
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