Date published: 2025-10-12

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NQO1 Activators

NQO1 activators predominantly act by modulating upstream pathways that ultimately lead to the induction or activation of NQO1. A majority of the chemicals listed induce NQO1 through the Nrf2 (nuclear factor erythroid 2-related factor 2) signaling pathway. Compounds like sulforaphane, tanshinone IIA, and curcumin have demonstrated effectiveness in activating the Nrf2-ARE (Antioxidant Response Element) pathway. Upon activation, Nrf2 translocates to the nucleus and binds to the ARE, facilitating the transcription of NQO1 among other cytoprotective enzymes. This biochemical action effectively results in increased levels of active NQO1 in the cell.

Another notable pathway involved is the AhR (Aryl Hydrocarbon Receptor) pathway, activated by beta-naphthoflavone. AhR, when activated, forms a complex that translocates to the nucleus and binds to the xenobiotic response element (XRE), inducing the expression of detoxification enzymes, including NQO1. Chemicals such as resveratrol and lycopene also act via Nrf2 but are unique in their biochemical interactions. For example, resveratrol, a polyphenolic compound, not only activates Nrf2 but also exhibits modulatory effects on various signaling molecules like SIRT1, thus offering a dual route for NQO1 activation. Ursolic acid, a triterpenoid, employs the Nrf2-ARE pathway but has been noted for its lipophilic nature, facilitating easier membrane permeability and effective intracellular action.

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