Abstract
The new of 1-(2-hydroxyethoxy)methylindole derivatives 3a-i were prepared in good yields. None of them showed any significant anti-HIV activity and therefore the benzocondensation between the 2 and 3 positions of the pyrrole ring definitely reduced the weak activity found in the analogues 1a-c.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Anti-HIV Agents / chemistry*
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Anti-HIV Agents / pharmacology
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Cell Line
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Chlorocebus aethiops
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Cytopathogenic Effect, Viral / drug effects
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Gram-Negative Bacteria / drug effects
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Gram-Positive Bacteria / drug effects
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HIV-1 / drug effects
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HIV-1 / pathogenicity
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Humans
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Indoles / chemistry*
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Microbial Sensitivity Tests
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Pyrroles / chemistry*
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Pyrroles / pharmacology
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Vero Cells
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Virus Replication / drug effects
Substances
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Anti-HIV Agents
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Indoles
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Pyrroles