Abstract
A versatile and broad range approach to previously unknown bis(indolyl)methane oximes based on two consecutive hetero Diels-Alder cycloaddition reactions of electrophilic conjugated nitrosoalkenes with indoles is disclosed. The cytotoxic properties and selectivity of some adducts against several human cancer cell lines pointing to a promising role in the development of anti-tumoural drugs, in particular for leukaemia and lymphoma.
Keywords:
Anti-cancer activity; Bis(indolyl)methanes; Indoles; Leukaemia; Lymphoma; Nitrosoalkenes.
Copyright © 2015 Elsevier Masson SAS. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antineoplastic Agents / adverse effects
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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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Cell Culture Techniques
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Cell Line, Tumor
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Cell Survival / drug effects
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Cycloaddition Reaction
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Drug Design*
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Humans
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Indoles / adverse effects
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Indoles / chemical synthesis*
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Indoles / chemistry
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Indoles / pharmacology
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Macrophages / drug effects
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Microglia / drug effects
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Oximes / adverse effects
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Oximes / chemical synthesis*
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Oximes / chemistry
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Oximes / pharmacology
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Structure-Activity Relationship
Substances
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Antineoplastic Agents
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Indoles
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Oximes