Paper
Structure-activity studies leading to potent chloride channel blockers: 5e-tert-Butyl-2-[4-(substituted-ethynyl)phenyl]-1,3-dithianes.
Published Dec 1, 1994 · Q. X. Li, J. Casida
Bioorganic & medicinal chemistry
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Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
5e-tert-Butyl-2-[4-(substituted-ethynyl)phenyl]-1,3-dithianes with selected functional groups are potent chloride channel blockers, with the R substituent's high activity being due to its polari
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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