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Bioorg Med Chem Lett. 2009 Mar 15;19(6):1745-8. doi: 10.1016/j.bmcl.2009.01.084. Epub 2009 Jan 30.

N-Benzyl-indolo carboxylic acids: Design and synthesis of potent and selective adipocyte fatty-acid binding protein (A-FABP) inhibitors.

Author information

1
Department of Medicinal Chemistry, Biovitrum AB, Research, 112 76 Stockholm, Sweden.

Abstract

Small molecule inhibitors of adipocyte fatty-acid binding protein (A-FABP) have gained renewed interest following the recent publication of pharmacologically beneficial effects of such inhibitors. Despite the potential utility of selective A-FABP inhibitors within the fields of metabolic disease, inflammation and atherosclerosis, there are few examples of useful A-FABP inhibitors in the public domain. Herein, we describe the optimization of N-benzyl-tetrahydrocarbazole derivatives through the use of co-crystal structure guided medicinal chemistry efforts. This led to the identification of a potent and selective class of A-FABP inhibitors as illustrated by N-benzyl-hexahydrocyclohepta[b]indole 30.

PMID:
19217286
DOI:
10.1016/j.bmcl.2009.01.084
[Indexed for MEDLINE]

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