The Macamide N-3-Methoxybenzyl-Linoleamide Is a Time-Dependent Fatty Acid Amide Hydrolase (FAAH) Inhibitor

Author:

Almukadi Haifa,Wu Hui,Böhlke Mark,Kelley Charles J.,Maher Timothy J.,Pino-Figueroa Alejandro

Publisher

Springer Science and Business Media LLC

Subject

Neuroscience (miscellaneous),Cellular and Molecular Neuroscience,Neurology

Reference42 articles.

1. Pino-Figueroa A (2009) In vivo and in vitro neuroprotective effects of the pentane soluble compounds from Lepidium meyenii (Maca). Dissertation, Massachusetts College of Pharmacy and Health Sciences University

2. Pino-Figueroa A, Nguyen D, Maher TJ (2010) Neuroprotective effects of Lepidium meyenii (Maca). Ann N Y Acad Sci 1199:77–85

3. Pino-Figueroa A, Vu H, Kelley CJ, Maher TJ (2011) Mechanism of action of Lepidium meyenii (Maca): an explanation for its neuroprotective activity. Am J Neuroprotec Neuroregen 3:87–92

4. Wu H (2011) Macamides and their synthetic analogs as potential FAAH inhibitors. Dissertation, Massachusetts College of Pharmacy and Health Sciences University

5. Vu H., (2012) Fatty acid amide hydrolase (FAAH) inhibitors: discovery in Lepidium meyenii (Maca) extracts. In: Conference Proceedings of The National Conference On Undergraduate Research (NCUR), Weber State University, Utah, 29–31 March 2012, 410-417

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