Abstract
17beta-O-Alkyl ethers (methyl, ethyl, propyl, butyl, hexyl, and octyl) of estradiol were obtained from 3-O-benzyl-17beta-estradiol with sodium hydride/alkyl halide, followed by the removal of the O-benzyl protecting group via catalytic transfer hydrogenation. An increase compared to estradiol in the protection of neural (HT-22) cells against oxidative stress due to exposure of glutamate was furnished by higher (C-3 to C-8) alkyl ethers, while methyl and ethyl ethers decreased the neuroprotective effect significantly. Lipophilic (butyl and octyl) ethers blocking the phenolic hydroxyl (3-OH) of A-ring were inactive.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Benzyl Compounds / chemical synthesis*
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Benzyl Compounds / chemistry
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Benzyl Compounds / pharmacology
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Cell Line
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Cell Survival / drug effects
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Crystallography, X-Ray
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Estradiol / analogs & derivatives*
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Estradiol / chemical synthesis*
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Estradiol / chemistry
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Estradiol / pharmacology
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Mice
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Neuroprotective Agents / chemical synthesis*
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Neuroprotective Agents / chemistry
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Neuroprotective Agents / pharmacology
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Oxidative Stress / drug effects*
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Structure-Activity Relationship
Substances
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Benzyl Compounds
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Neuroprotective Agents
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Estradiol