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Merck
CN

SML0361

3′,4′-Dihydroxyflavonol

≥98% (HPLC)

Synonym(s):

2-(3,4-Dihydroxyphenyl)-3-hydroxy-4H-benzopyran-4-one, 3, 3′, 4′-Trihydroxyflavone, DiOHF, 5,7-Dideoxyquercetin

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About This Item

Empirical Formula (Hill Notation):
C15H10O5
CAS Number:
6068-78-6
Molecular Weight:
270.24
NACRES:
NA.77
PubChem Substance ID:
329825363
UNSPSC Code:
12352200
MDL number:
MFCD00189455

Key Documents

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InChI

1S/C15H10O5/c16-10-6-5-8(7-11(10)17)15-14(19)13(18)9-3-1-2-4-12(9)20-15/h1-7,16-17,19H

SMILES string

Oc1ccc(cc1O)C2=C(O)C(=O)c3ccccc3O2

InChI key

KPGMHZQXQVDYNT-UHFFFAOYSA-N

assay

≥98% (HPLC)

form

powder

storage condition

protect from light

color

faintly yellow to dark yellow

solubility

DMSO: >15 mg/mL

storage temp.

2-8°C

Quality Level

100

Biochem/physiol Actions

3′,4′-Dihydroxyflavonol is a synthetic cardioprotective flavone that attenuates myocardial ischemia/reperfusion injury, which associated with its antioxidant activity.
3′,4′-Dihydroxyflavonol is a synthetic cardioprotective flavone; antioxidant.

pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H301

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
0000484838
0000484838
0000442441
0000442440
0000442440

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Kyuichi Kawabata et al.
Bioscience, biotechnology, and biochemistry, 79(5), 799-807 (2015-02-28)
Probiotics have been shown to improve the condition of not only the human gastrointestinal tract but also the entire body. We found that quercetin enhances the anti-inflammatory activity of Bifidobacterium adolescentis, which is abundant in human intestines. Here, we assessed

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