Mar. Drugs 2014, 12(2), 601-635; doi:10.3390/md12020601

Targeting Nuclear Receptors with Marine Natural Products

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Received: 12 November 2013; in revised form: 20 December 2013 / Accepted: 7 January 2014 / Published: 27 January 2014
(This article belongs to the Special Issue Mechanism of Action Analysis for Marine Compounds)
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Nuclear receptors (NRs) are important pharmaceutical targets because they are key regulators of many metabolic and inflammatory diseases, including diabetes, dyslipidemia, cirrhosis, and fibrosis. As ligands play a pivotal role in modulating nuclear receptor activity, the discovery of novel ligands for nuclear receptors represents an interesting and promising therapeutic approach. The search for novel NR agonists and antagonists with enhanced selectivities prompted the exploration of the extraordinary chemical diversity associated with natural products. Recent studies involving nuclear receptors have disclosed a number of natural products as nuclear receptor ligands, serving to re-emphasize the translational possibilities of natural products in drug discovery. In this review, the natural ligands of nuclear receptors will be described with an emphasis on their mechanisms of action and their therapeutic potentials, as well as on strategies to determine potential marine natural products as nuclear receptor modulators.
Keywords: nuclear receptors; marine natural products; ligands; screen; drug targets
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MDPI and ACS Style

Yang, C.; Li, Q.; Li, Y. Targeting Nuclear Receptors with Marine Natural Products. Mar. Drugs 2014, 12, 601-635.

AMA Style

Yang C, Li Q, Li Y. Targeting Nuclear Receptors with Marine Natural Products. Marine Drugs. 2014; 12(2):601-635.

Chicago/Turabian Style

Yang, Chunyan; Li, Qianrong; Li, Yong. 2014. "Targeting Nuclear Receptors with Marine Natural Products." Mar. Drugs 12, no. 2: 601-635.

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