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Cited by 333

The DOI matches its Crossref record; 45 of the 45 references it cites were found in a registry or an index.

Natural product-derived pharmacological modulators of Nrf2/ARE pathway for chronic diseases

Kumar, Hemant, Kim, In-Su, More, Sandeep Vasant, Kim, Byung-Wook, Choi, Dong-Kug·2014·Nat. Prod. Rep.

Abstract

Covering: 2000 to 2013. Oxidative stress is the central component of chronic diseases. The nuclear factor erythroid 2-related factor 2/antioxidant response element (Nrf2/ARE) pathway is vital in the up-regulation of cytoprotective genes and enzymes in response to oxidative stress and treatment with certain dietary phytochemicals. Herein, we classify bioactive compounds derived from natural products that are Nrf2/ARE pathway activators and recapitulate the molecular mechanisms for inducing Nrf2 to provide favorable effects in experimental models of chronic diseases. Moreover, pharmacological inhibition of Nrf2 signalling has emerged as promising strategy against multi-drug resistance thereby improving the treatment efficacy. We have also enlisted natural product-derived inhibitors of Nrf2/ARE pathway.

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Metadata

Authors
Kumar, H., Kim, I.-S., More, S. V., Kim, B.-W., & Choi, D.-K.
Venue
Nat. Prod. Rep.
Published
2014
Volume
31
Issue
1
Pages
109-139
ISSN
  • 0265-0568 (ISSN-L)
  • 1460-4752
OpenAlex
W2100123437
Cited by
333
References
45
FWCI
7.93
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Natural product-derived pharmacological modulators of Nrf2/ARE pathway for chronic diseases. https://app.cochat.ai/papers/10.1039/c3np70065h
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Kumar, H., Kim, I.-S., More, S. V., Kim, B.-W., & Choi, D.-K. (2014). Natural product-derived pharmacological modulators of Nrf2/ARE pathway for chronic diseases. Nat. Prod. Rep. https://doi.org/10.1039/c3np70065h

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.