A CNS-Targeting Prodrug Strategy for Nuclear Receptor Modulators
- J Med Chem. 2020 Sep 10;63(17):9742-9751. doi: 10.1021/acs.jmedchem.0c00868.
- 1. Department of Chemical Physiology and Biochemistry, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, Oregon 97239, United States.
The blood-brain barrier is a major impediment for targeted central nervous system (CNS) therapeutics, especially with carboxylic acid-containing drugs. Nuclear receptor modulators, which often feature carboxylic acid motifs for target engagement, have emerged as a class of potentially powerful therapeutics for neurodegenerative CNS diseases. Herein is described a prodrug strategy that directs the biodistribution of parent drug nuclear receptor modulators into the CNS while masking them as functional receptor ligands in the periphery. This prodrug strategy targets a specific amidase, fatty acid amide hydrolase (FAAH), an enzyme with enriched expression in the CNS. Our results demonstrate that this prodrug strategy can be generalized to a variety of carboxylic acid-containing drug structures that satisfy the structural requirements of blood-brain barrier diffusion and FAAH substrate recognition.
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Cat. No.Product NameDescriptionTargetResearch Area
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target: Drug IntermediateResearch Areas: Neurological Disease
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target: FAAH
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target: MMPResearch Areas: Neurological Disease