Abstract
A number of 2-(1H-indol-3-yl)quinoline-3-carbonitrile derivatives were synthesized via AlCl(3)-mediated C-C bond forming reaction between 2-chloroquinoline-3-carbonitrile and various indoles. The methodology does not require any N-protection of the indoles employed and provided the corresponding products in good yields. The molecular structure of a representative compound was established unambiguously by single crystal X-ray diffraction and structural elaboration of a compound synthesized has been demonstrated. Many of these compounds synthesized showed PDE4 inhibitory properties in vitro. A brief structure-activity relationship studies within the series along with docking results of a representative compound (EC(50) ∼0.89 μM) is presented.
Copyright © 2012 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Aluminum Chloride
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Aluminum Compounds / chemistry
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Binding Sites
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Carbon / chemistry
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Cell Proliferation / drug effects
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Chlorides / chemistry
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Computer Simulation
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Crystallography, X-Ray
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Cyclic Nucleotide Phosphodiesterases, Type 4 / chemistry*
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Cyclic Nucleotide Phosphodiesterases, Type 4 / metabolism
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HEK293 Cells
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Humans
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Indoles / chemistry
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Molecular Conformation
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Phosphodiesterase 4 Inhibitors / chemical synthesis*
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Phosphodiesterase 4 Inhibitors / chemistry
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Phosphodiesterase 4 Inhibitors / pharmacology
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Quinolines / chemical synthesis
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Quinolines / chemistry*
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Quinolines / pharmacology
Substances
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Aluminum Compounds
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Chlorides
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Indoles
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Phosphodiesterase 4 Inhibitors
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Quinolines
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Aluminum Chloride
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Carbon
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quinoline
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Cyclic Nucleotide Phosphodiesterases, Type 4
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2-chloroquinoline