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411035

Sigma-Aldrich

6-Hydroxyflavone

98%

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About This Item

Empirical Formula (Hill Notation):
C15H10O3
CAS Number:
Molecular Weight:
238.24
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

solid

mp

234-236 °C (lit.)

functional group

ketone
phenyl

SMILES string

Oc1ccc2OC(=CC(=O)c2c1)c3ccccc3

InChI

1S/C15H10O3/c16-11-6-7-14-12(8-11)13(17)9-15(18-14)10-4-2-1-3-5-10/h1-9,16H

InChI key

GPZYYYGYCRFPBU-UHFFFAOYSA-N

Gene Information

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Zia Ud Din et al.
Histology and histopathology, 35(10), 1197-1209 (2020-09-11)
In this study, the flavonoid, 6-hydroxyflavone was investigated for its renal protective activity in the cisplatin rat model of nephrotoxicity. Male Sprague-Dawley rats weighing 200-250 g were included in the study. 6-Hydroxyflavone was daily administered at 25 and 50 mg/kg
Structure of 6-hydroxyflavone.
Seetharaman J and Rajan SS.
Acta Crystallographica Section C, Structural Chemistry, 48(9), 1714-1715 (1992)
Xing Wang et al.
PloS one, 10(3), e0116409-e0116409 (2015-03-20)
Inflammatory responses by kidney mesangial cells play a critical role in the glomerulonephritis. The anti-inflammatory potential of nineteen mono-, di- and polyhydroxylated flavones including fisetin, quercetin, morin, tricetin, gossypetin, apigenin and myricetin were investigated on rat mesangial cells with lipopolysaccharide
Chien-Hung Lai et al.
Evidence-based complementary and alternative medicine : eCAM, 2014, 924560-924560 (2014-05-06)
Osteoblast differentiation plays an essential role in bone integrity. Isoflavones and some flavonoids are reported to have osteogenic activity and potentially possess the ability to treat osteoporosis. However, limited information concerning the osteogenic characteristics of hydroxyflavones is available. This study
A novel and facile iodine (III)-mediated approach for C (5)-acetoxylation of 6-hydroxyflavone and 6-hydroxyflavanones.
Prakash O, et al.
Tetrahedron Letters, 45(49), 9065-9067 (2004)

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