A diol form of (±)12,13-EpOME
Related Products
Labeled Version(s)
10009994(±)12(13)-DiHOME-d4
Parent Compound(s)
52450(±)12(13)-EpOME
Technical Support & Resources

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(±)12(13)-DiHOME

Item No. 10009832

Technical Information
Formal Name
12,13-dihydroxy-9Z-octadecenoic acid
CAS Number
263399-35-5
Synonyms
  • Isoleukotoxin diol
Molecular Formula
C18H34O4
Formula Weight
Purity
≥98%
A 100 µg/ml solution in methyl acetate
DMF: 20 mg/mlDMSO: 20 mg/mlEthanol: 20 mg/mlPBS (pH 7.2): 10 µg/ml
SMILES
CCCCC[C@@H](O)[C@H](O)C/C=C\CCCCCCCC(O)=O
InChi Code
InChI=1S/C18H34O4/c1-2-3-10-13-16(19)17(20)14-11-8-6-4-5-7-9-12-15-18(21)22/h8,11,16-17,19-20H,2-7,9-10,12-15H2,1H3,(H,21,22)/b11-8-/t16-,17-/m1/s1
InChi Key
CQSLTKIXAJTQGA-RIDHJDLKSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    Product Description

    (±)12(13)-DiHOME is the diol form of (±)12(13)-EpOME (Item No. 52450), a cytochrome P450-derived epoxide of linoleic acid (Item Nos. 90150 | 90150.1 | 21909) also known as isoleukotoxin.1 It is formed from 12(13)-EpOME by soluble epoxide hydrolase (sEH) in neutrophils.2 12(13)-DiHOME is toxic to Sf21 cells expressing sEH and to lacZ-expressing control cells, unlike isoleukotoxin, which is only toxic to cells containing sEH.1,2 Levels of 12(13)-DiHOME are increased in rat spinal cord following burn injury, and it enhances cold tolerance, increases fatty acid uptake into brown adipocytes, and decreases serum triglyceride levels in mice.3,4 Levels are also elevated in bronchoalveolar lavage fluid (BALF) in humans following exposure to biodiesel exhaust and in exhaled breath condensate in patients with allergic asthma following allergen exposure.5,6 Plasma levels of 12(13)-DiHOME are increased immediately following moderate-intensity exercise in mice and humans, an effect that can be prevented by brown adipose tissue removal in the mouse.7

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Greene, J.F., Williamson, K.C., Newman, J.W., et alMetabolism of monoepoxides of methyl linoleate: Bioactivation and detoxification. Arch. Biochem. Biophys. 376(2), 420-432 (2000).

    2. Moghaddam, M.F., Grant, D.F., Cheek, J.M., et alBioactivation of leukotoxins to their toxic diols by epoxide hydrolase. Nat. Med. 3(5), 562-566 (1997).

    3. Green, D.P., Ruparel, S., Gao, X., et alCentral activation of TRPV1 and TRPA1 by novel endogenous agonists contributes to mechanical allodynia and thermal hyperalgesia after burn injury. Mol. Pain 12, (2016).

    4. Lynes, M.D., Leiria, L.O., Lundh, M., et alThe cold-induced lipokine 12,13-diHOME promotes fatty acid transport into brown adipose tissue. Nat. Med. 23(5), 631-637 (2017).

    5. Gouveia-Figueira, S., Karimpour, M., Bosson, J.A., et alMass spectrometry profiling of oxylipins, endocannabinoids, and N-acylethanolamines in human lung lavage fluids reveals responsiveness of prostaglandin E2 and associated lipid metabolites to biodiesel exhaust exposure. Anal. Bioanal. Chem. 409(11), 2967-2980 (2017).

    6. Nording, M.L., Yang, J., Hegedus, C.M., et alEndogenous levels of five fatty acid metabolites in exhaled breath condensate to monitor asthma by high-performance liquid chromatography: Electrospray tandem mass spectrometry. IEEE Sens. J. 10(1), 123-130 (2010).

    7. Stanford, K.I., Lynes, M.D., Takahashi, H., et al12,13-diHOME: An exercise-induced lipokine that increases skeletal muscle fatty acid uptake. Cell Metab. 27(5), 1111-1120 (2018).

    Product Citations

    Bracken, O.V., Jalali, P., Glanville, J.R.W., et alEpoxy-oxylipins direct monocyte fate in inflammatory resolution in humans. Nat. Commun. 17(1), 431 (2026).

    Matsumoto, K., Takada, Y., Imamura, Y., et alLive and heat-treated Lactiplantibacillus plantarum induce distinct metabolic and immune responses in intestinal epithelial cells. iScience 29(5), 115516 (2026).

    Nirengi, S., Buck, B., Das, D., et al12,13-diHOME protects against the age-related decline in cardiovascular function via attenuation of CaMKII. Nat. Commun. 16(1), 7088 (2025).

    Wu, Z., Xiao, H., Rao, D., et alAnalytical strategy for oxylipin annotation by combining chemical derivatization-based retention index algorithm and feature tandem mass spectrometric fragmentation as a biomarker discovery tool. Anal. Chem. 95(43), 15933-15942 (2023).

    Gouveia-Figueira, S., Karlsson, J., Deplano, A., et alCharacterisation of (R)-2-(2-fluorobiphenyl-4-yl)-N-(3-methylpyridin-2-yl)propanamide as a dual fatty acid amide hydrolase: Cyclooxygenase inhibitor. PLoS One 10(9), e0139212 (2015).