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3,5-bis((E)-3-methoxybenzylidene)-1-methylpiperidin-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1401079-68-2

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1401079-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1401079-68-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,1,0,7 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1401079-68:
(9*1)+(8*4)+(7*0)+(6*1)+(5*0)+(4*7)+(3*9)+(2*6)+(1*8)=122
122 % 10 = 2
So 1401079-68-2 is a valid CAS Registry Number.

1401079-68-2Downstream Products

1401079-68-2Relevant academic research and scientific papers

Activation of anti-oxidant Nrf2 signaling by enone analogues of curcumin

Deck, Lorraine M.,Hunsaker, Lucy A.,Vander Jagt, Thomas A.,Whalen, Lisa J.,Royer, Robert E.,Vander Jagt, David L.

, p. 854 - 865 (2018)

Inflammation and oxidative stress are common in many chronic diseases. Targeting signaling pathways that contribute to these conditions may have therapeutic potential. The transcription factor Nrf2 is a major regulator of phase II detoxification and anti-oxidant genes as well as anti-inflammatory and neuroprotective genes. Nrf2 is widespread in the CNS and is recognized as an important regulator of brain inflammation. The natural product curcumin exhibits numerous biological activities including ability to induce the expression of Nrf2-dependent phase II and anti-oxidant enzymes. Curcumin has been examined in a number of clinical studies with limited success, mainly owing to limited bioavailability and rapid metabolism. Enone analogues of curcumin were examined with an Nrf2 reporter assay to identify Nrf2 activators. Analogues were separated into groups with a 7-carbon dienone spacer, as found in curcumin; a 5-carbon enone spacer with and without a ring; and a 3-carbon enone spacer. Activators of Nrf2 were found in all three groups, many of which were more active than curcumin. Dose-response studies demonstrated that a range of substituents on the aromatic rings of these enones influenced not only the sensitivity to activation, reflected in EC50 values, but also the extent of activation, which suggests that multiple mechanisms are involved in the activation of Nrf2 by these analogues.

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