Wedelolactone

Wedelolactone

Catalog Number:
L002373310APE
Mfr. No.:
APE-N2131
Price:
$378
  • Size:
    20mg
    Quantity:
    Add to Cart:
      • Overview
        • Please contact us at for specific academic pricing.

          Background

          Wedelolactone is an inhibitor of IKK.IkB kinase (IKK) complex contains the catalytic subunits IKKα and IKKβ, and the regulatory subunit IKKγ/NEMO. IKK, is a kinase critical for activation of NF-κB by mediating phosphorylation and degradation of IκBα. The induction of caspase-11 is an important upstream controlling event in inflammatory response and apoptosis under pathological conditions modulated by upstream NF-κB-mediated transcription[1].In vitro: In cultured mouse BALB/c 3T3 cells, mouse splenocytes and HeLa cells, wedelolactone (0~100 μM) inhibited LPS-induced caspase-11 expression by inhibiting NF-κB-mediated transcription through the direct inhibition of IKK. Wedelolactone played an potential role in anti-inflammatory therapy to inhibit IL-1β levels in diseases such as rheumatoid arthritis, asthma and septic shock[1].In vivo: On Swiss albino male mouse skin, IKK inhibition by wedelolactone (10 μM) prevented the induction of NF-κB, perturbed the generation of reactive oxygen species and reactive nitrogen intermediates, blunted the signal transduction that lead to the activation of the early immediate genes, and thereby protected mouse skin from the UVB induced neoplastic transformation, angiotropism and metastatic progression [2].

          [1] Kobori M, Yang Z, Gong D, et al. Wedelolactone suppresses LPS-induced caspase-11 expression by directly inhibiting the IKK complex.[J]. Cell Death & Differentiation, 2004, 11(1):123-30.
          [2] Ali F, Khan B A, Sultana S. Wedelolactone mitigates UVB induced oxidative stress, inflammation and early tumor promotion events in murine skin: plausible role of NFκB pathway[J]. European Journal of Pharmacology, 2016, 786:253-264.

      • Properties
        • Alternative Name
          1,8,9-trihydroxy-3-methoxy-[1]benzofuro[3,2-c]chromen-6-one
          CAS Number
          524-12-9
          Molecular Formula
          C16H10O7
          Molecular Weight
          314.25
          Purity
          98.00%
          Solubility
          insoluble in EtOH; insoluble in H2O; ≥44.4 mg/mL in DMSO
          Storage
          Store at -20°C

          * For Research Use Only

      • Reference
        • 1. Zhong X, Liu M, et al. "Epigallocatechin-3-Gallate Attenuates Microglial Inflammation and Neurotoxicity by Suppressing the Activation of Canonical and Non-Canonical Inflammasome via TLR4/NF-κB Pathway." Mol Nutr Food Res. 2019 Aug 2:e1801230. PMID:31374144

    Note: If you don't receive our verification email, do the following:

    Copyright © Amerigo Scientific. All rights reserved.