Abstract
We report the synthesis and the anti-HIV activities of new C2-symmetrical and achiral N1,N3-dibenzyl-2-hydroxy-propane isosteres. Some of them showed significant inhibitory activity with respect to HIV-infected MT4 cells (compound 6a and 7a, IC50 = 0.1 microM). These new structurally simple compounds represent new synthons which can be suitable for combinatorial chemistry purposes.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Anti-HIV Agents / chemical synthesis*
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Anti-HIV Agents / chemistry
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Anti-HIV Agents / pharmacology*
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Benzylamines / chemical synthesis*
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Benzylamines / chemistry
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Benzylamines / pharmacology*
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Cell Line
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Humans
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Propanolamines / chemical synthesis*
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Propanolamines / chemistry
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Propanolamines / pharmacology*
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Structure-Activity Relationship
Substances
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Anti-HIV Agents
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Benzylamines
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Propanolamines