Abstract
A new series of diarylmethylnapthyloxy ethylamines were synthesized by aminoalkylation of diarylmethylnaphthols which were obtained by Friedel-Crafts alkylation on 1- and 2-naphthols using diarylcarbinols as the alkylating agents. The title compounds were evaluated for antitubercular activity against Mycobacterium tuberculosis H(37)R(v) in vitro and showed MIC in the range of 3.12-25 microg/ml.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antitubercular Agents / chemical synthesis*
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Antitubercular Agents / chemistry
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Antitubercular Agents / pharmacology*
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Drug Design*
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Methylation
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Molecular Structure
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Mycobacterium tuberculosis / drug effects*
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Naphthols / chemical synthesis*
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Naphthols / chemistry
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Naphthols / pharmacology*
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Structure-Activity Relationship
Substances
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Antitubercular Agents
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Naphthols