الصفحة الرئيسية>>Signaling Pathways>> Proteases>> Lipoxygenase>>9(S)-HODE-13C18

9(S)-HODE-13C18 (Synonyms: (+)-α-Dimorphecolic Acid)

رقم الكتالوجGC46755

A neuropeptide with diverse biological activities

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9(S)-HODE-13C18 التركيب الكيميائي

Cas No.: N/A

الحجم السعر المخزون الكميّة
25 μg
214٫00
متوفر
50 μg
408٫00
متوفر
100 μg
770٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.

Description of 9(S)-HODE-13C18

9(S)-HODE-13C18 is intended for use as an internal standard for the quantification of 9(S)-HODE by GC- or LC-MS. 9(S)-HODE is a monohydroxy fatty acid formed from linoleic acid primarily by lipoxygenases with a 9-HpODE intermediate.1,2,3,4 It is an agonist of PPARγ, inducing transcription of AF-2 in a reporter assay when used at a concentration of 20 µM, and enhances the production of primary human chorionic gonadotropin (hCG) in trophoblasts.5 9(S)-HODE is also an agonist of transient receptor potential vanilloid 1 (TRPV1), TRP ankyrin 1 (TRPA1), and TRP melastatin 8 (TRPM8), increasing intracellular calcium levels in HEK293 cells (EC50s = 21, 31.9, and 43.6 µM, respectively, for the human receptors).6 It inhibits the migration of primary porcine aortic endothelial cells and phytohemagglutinin-induced migration of human mononuclear cells when used at concentrations ranging from 0.01 to 1 µM.7

1.Vick, B.A.Oxygenated fatty acids of the lipoxygenase pathwayLipid Metabolism in Plants167-191(1993) 2.Reinaud, O., Delaforge, M., Boucher, J.L., et al.Oxidative metabolism of linoleic acid by human leukocytesBiochem. Biophys. Res. Commun.161(2)883-891(1989) 3.Kim, E., Rundhaug, J.E., Benavides, F., et al.An antitumorigenic role for murine 8S-lipoxygenase in skin carcinogenesisOncogene24(7)1174-1187(2005) 4.Hamberg, M.Stereochemistry of oxygenation of linoleic acid catalyzed by prostaglandin-endoperoxide H synthase-2Arch. Biochem. Biophys.349(2)376-380(1998) 5.Schild, R.L., Schaiff, W.T., Carolson, M.G., et al.The activity of PPARγ in primary human trophoblasts is enhanced by oxidized lipidsJ. Clin. Endocrinol. Metab.87(3)1105-1110(2002) 6.De Petrocellis, L., Moriello, A.S., Imperatore, R., et al.A re-evaluation of 9-HODE activity at TRPV1 channels in comparison with anandamide: enantioselectivity and effects at other TRP channels and in sensory neuronsBr. J. Pharmacol.167(8)1643-1651(2012) 7.Pankonin, G., Mahmood, S.A., Kuhn, H., et al.Inhibition of cell migrations by the linoleic acid oxygenation product 9S-hydroxy 10E,12Z octadecadienoic acid (9-HODE)Biomed. Biochim. Acta.47(12)K17-21(1988)

Chemical Properties of 9(S)-HODE-13C18

Cas No. N/A SDF
المرادفات (+)-α-Dimorphecolic Acid
Canonical SMILES O[13C]([13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13C@H](O)/[13CH]=[13CH]/[13CH]=[13CH]\[13CH2][13CH2][13CH2][13CH2][13CH3])=O
Formula [13C]18H32O3 M.Wt 314.3
الذوبان DMF: 50 mg/ml,DMSO: 50 mg/ml,Ethanol: 50 mg/ml,PBS (pH 7.2): 1 mg/ml Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of 9(S)-HODE-13C18

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 3.1817 mL 15.9084 mL 31.8167 mL
5 mM 0.6363 mL 3.1817 mL 6.3633 mL
10 mM 0.3182 mL 1.5908 mL 3.1817 mL
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In vivo Formulation Calculator (Clear solution) of 9(S)-HODE-13C18

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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

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Average Rating: 5 ★★★★★ (Based on Reviews and 23 reference(s) in Google Scholar.)

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