A derivative of jasmonic acid
Related Products
Isomer(s)
40227CAY10799 (potassium salt)
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(±)-Tuberonic Acid

Item No. 35750

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
2-[(2Z)-5-hydroxy-2-penten-1-yl]-3-oxo-cyclopentaneacetic acid
CAS Number
221682-86-6
Synonyms
  • 12-hydroxy Jasmonic Acid
  • 12-hydroxy epi-Jasmonic Acid
Molecular Formula
C12H18O4
Formula Weight
226.3
Purity
≥70%
Formulation (Request formulation change)
A 10 mg/ml solution in methanol
Solubility(Learn about Variance in Solubility)
Methanol: Slightly
SMILES
OC(CC1C(C(CC1)=O)C/C=C\CCO)=O
InChi Code
InChI=1S/C12H18O4/c13-7-3-1-2-4-10-9(8-12(15)16)5-6-11(10)14/h1-2,9-10,13H,3-8H2,(H,15,16)/b2-1-
InChi Key
RZGFUGXQKMEMOO-UPHRSURJSA-N
Origin
Synthetic
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    1 mg

    $49

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    5 mg

    $218

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    10 mg

    $387

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    25 mg

    $845

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    Product Description

    (±)-Tuberonic acid is a derivative of the plant growth regulator jasmonic acid (Item No. 88300) that has been found in M. oleifera.1,2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Seto, Y., Hamada, S., Ito, H., et al. Tobacco salicylic acid glucosyltransferase is active toward tuberonic acid (12-hydroxyjasmonic acid) and is induced by mechanical wounding stress. Biosci. Biotechnol. Biochem. 75(12), 2316-2320 (2011).

    2. Luetragoon, T., Sranujit, R.P., Noysang, C., et al. Bioactive compounds in Moringa oleifera Lam. leaves inhibit the pro-inflammatory mediators in Lipopolysaccharide-induced human monocyte-derived macrophages. Molecules 25(1), 191 (2020).