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SML0699

Sigma-Aldrich

4′-Methoxyflavone

≥97% (HPLC)

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Synonym(s):
2-(4-Methoxyphenyl)-4H-chromen-4-one, 2-(4-Methoxyphenyl)chromone
Empirical Formula (Hill Notation):
C16H12O3
CAS Number:
Molecular Weight:
252.26
EC Number:
NACRES:
NA.77

Assay

≥97% (HPLC)

form

lyophilized powder

storage condition

protect from light

color

white

solubility

DMSO: 5 mg/mL, clear (warmed)

storage temp.

2-8°C

InChI

1S/C16H12O3/c1-18-12-8-6-11(7-9-12)16-10-14(17)13-4-2-3-5-15(13)19-16/h2-10H,1H3

InChI key

OMICQBVLCVRFGN-UHFFFAOYSA-N

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This Item
D6571T4080SML3158
Sigma-Aldrich

Sigma-Aldrich

SML0699

4′-Methoxyflavone

6-Methylflavone ≥98% (HPLC)

Sigma-Aldrich

SML3158

6-Methylflavone

form

lyophilized powder

form

powder

form

powder

form

powder

storage condition

protect from light

storage condition

-

storage condition

desiccated, protect from light

storage condition

-

color

white

color

white to off-white

color

yellow

color

white to beige

solubility

DMSO: 5 mg/mL, clear (warmed)

solubility

DMSO: ≥20 mg/mL

solubility

DMSO: >5 mg/mL

solubility

DMSO: 2 mg/mL, clear (warmed)

storage temp.

2-8°C

storage temp.

room temp

storage temp.

room temp

storage temp.

2-8°C

Biochem/physiol Actions

4-methoxyflavone is a neuroprotective agent that inhibits the accumulation of poly (ADP-ribose) and neuronal cell death following chemically-induced DNA damage or NMDA excitation.

Other Notes

Light sensitive.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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R N Gacche et al.
Archives of biochemistry and biophysics, 577-578, 35-48 (2015-05-06)
Relationship between structural diversity and biological activities of flavonoids has remained an important discourse in the mainstream of flavonoid research. In the current study anti-angiogenic, cytotoxic, antioxidant and cyclooxygenase (COX) inhibitory activities of diverse class of flavonoids including hydroxyl and

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