Abstract
In our study, a series of new harmine derivatives has been prepared by cycloaddition reaction using various arylnitrile oxides and evaluated in vitro against acetylcholinesterase and 5-lipoxygenase enzymes, MCF7 and HCT116 cancer cell lines. Some of these molecules have been shown to be potent inhibitors of acetylcholinesterase and MCF7 cell line. The greatest activity against acetylcholinesterase (IC50 = 10.4 µM) was obtained for harmine 1 and cytotoxic activities (IC50 = 0.2 µM) for compound 3a. Two derivatives 3e and 3f with the thiophene and furan systems, respectively, showed good activity against 5- lipoxygenase enzyme (IC50 = 29.2 and 55.5 µM, respectively).
Keywords:
1,3-dipolar cycloaddition; Peganum harmala; anti-5-lipoxygenase; anti-acetylcholinesterase; anti-cancer; harmine; oxazolines.
MeSH terms
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Acetylcholinesterase / metabolism
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Alzheimer Disease / drug therapy*
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Alzheimer Disease / enzymology
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Alzheimer Disease / metabolism
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Anti-Inflammatory Agents / chemical synthesis
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Anti-Inflammatory Agents / chemistry
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Anti-Inflammatory Agents / pharmacology*
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Antineoplastic Agents / chemical synthesis*
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Antineoplastic Agents / chemistry
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Antineoplastic Agents / pharmacology*
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Arachidonate 5-Lipoxygenase / metabolism
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Cell Proliferation / drug effects
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Cholinesterase Inhibitors / chemical synthesis
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Cholinesterase Inhibitors / chemistry
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Cholinesterase Inhibitors / pharmacology
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Dose-Response Relationship, Drug
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Drug Screening Assays, Antitumor
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HCT116 Cells
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Harmine / chemistry*
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Humans
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Inflammation / drug therapy*
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Isoxazoles / chemical synthesis
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Isoxazoles / chemistry
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Isoxazoles / pharmacology*
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Lipoxygenase Inhibitors / chemical synthesis
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Lipoxygenase Inhibitors / chemistry
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Lipoxygenase Inhibitors / pharmacology
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MCF-7 Cells
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Molecular Structure
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Structure-Activity Relationship
Substances
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Anti-Inflammatory Agents
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Antineoplastic Agents
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Cholinesterase Inhibitors
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Isoxazoles
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Lipoxygenase Inhibitors
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Harmine
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Arachidonate 5-Lipoxygenase
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Acetylcholinesterase