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SML0503

Sigma-Aldrich

9(S)-HODE

≥98% (HPLC)

Sinónimos:

9S-Hydroxy-10E,12Z-octadecadienoic acid

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About This Item

Fórmula empírica (notación de Hill):
C18H32O3
Número de CAS:
73543-67-6
Peso molecular:
296.44
EC Number:
200-578-6
MDL number:
MFCD00065831
UNSPSC Code:
51111800
PubChem Substance ID:
329825451
NACRES:
NA.77

Quality Level

100

assay

≥98% (HPLC)

form

solution

concentration

1 mg/mL in ethanol

color

colorless to light yellow

shipped in

wet ice

storage temp.

−20°C

SMILES string

CCCCC/C=C\C=C\[C@@H](O)CCCCCCCC(O)=O

InChI

1S/C18H32O3/c1-2-3-4-5-6-8-11-14-17(19)15-12-9-7-10-13-16-18(20)21/h6,8,11,14,17,19H,2-5,7,9-10,12-13,15-16H2,1H3,(H,20,21)/b8-6-,14-11+/t17-/m1/s1

Inchi Key

NPDSHTNEKLQQIJ-UINYOVNOSA-N

Biochem/physiol Actions

9(S)-HODE is produced by the lipoxygenation of linoleic acid. It is a major component of plasma oxidized low-density lipoprotein. 9-HODE has been shown to stimulate cell proliferation and and extracellular matrix synthesis in human mesangial cells via PPARgamma. Pro-inflammatory effects of 9-HODE, acting through the receptor GPR132, can contribute to atherosclerosis progression. 9-HODE has also been shown to activate spinal TRPV1, leading to inflammatory hyperalgesia.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

hcodes

H225,H319

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

57.2 °F - closed cup

flash_point_c

14.0 °C - closed cup

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The Biochemical journal, 420(2), 277-281 (2009-03-07)
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Journal of immunology (Baltimore, Md. : 1950), 172(1), 54-60 (2003-12-23)
Because of its oxidative modification during the acute-phase response to an aggression, low density lipoprotein (LDL) can be regarded as a source of lipid mediators that can act both to promote and inhibit inflammation. This can be exemplified by the
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