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2000
Volume 7, Issue 10
  • ISSN: 1570-1808
  • E-ISSN: 1875-628X

Abstract

In vitro radical-cation scavenging capacity and anti-AChE activities of 19 piperidine derivatives, including dihydrospiro[ piperidine-4,2'(1'H)quinolines] 7-19 and their precursor 4-allyl-4-arylaminopiperidines 1-6 were reported. Their data of bioassays and calculated logP and TPSA parameters showed promising drug-like properties. The best radical scavenging compound (TEAC 1.73 ± 0.01), 6-methyl-3',4'- dihydrospiro[piperidine-4,2'(1'H)quinoline] 8 showed IC50 value of 62.5 μM (20.0 μg/mL) using AChE assay.

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/content/journals/lddd/10.2174/1570180811007010710
2010-12-01
2025-09-04
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/content/journals/lddd/10.2174/1570180811007010710
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