Loading…

Development of Selective Butyrylcholinesterase Inhibitors Using (R)-Lipoic Acid-Polyphenol Hybrid Molecules

A series of hybrid molecules between (R)-lipoic acid (ALA) and the acetylated or methylated polyphenol compounds were synthesized and their in vitro cholinesterase [acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE)] inhibition activities were checked. The IC_50 values of all hybrid molec...

Full description

Saved in:
Bibliographic Details
Published in:Bulletin of the Korean Chemical Society 2011, 32(8), , pp.2997-3002
Main Authors: Woo, Yeun-Ji, Lee, Bo-Hyun, Yeun, Go-Heum, Kim, Hyun-Ju, Ko, Jang-Myoun, Won, Moo-Ho, Lee, Bong-Ho, Park, Jeong-Ho
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c327t-e01752c08669a168595409d3e73a529c592f898a5f4e52b1e548b573b3e6bab23
cites cdi_FETCH-LOGICAL-c327t-e01752c08669a168595409d3e73a529c592f898a5f4e52b1e548b573b3e6bab23
container_end_page 3002
container_issue spc8
container_start_page 2997
container_title Bulletin of the Korean Chemical Society
container_volume 32
creator Woo, Yeun-Ji
Lee, Bo-Hyun
Yeun, Go-Heum
Kim, Hyun-Ju
Ko, Jang-Myoun
Won, Moo-Ho
Lee, Bong-Ho
Park, Jeong-Ho
description A series of hybrid molecules between (R)-lipoic acid (ALA) and the acetylated or methylated polyphenol compounds were synthesized and their in vitro cholinesterase [acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE)] inhibition activities were checked. The IC_50 values of all hybrid molecules for a BuChE inhibition were lower than those of the single parent compounds. Specifically, ALA-acetyl protected caffeic acid (11,ALA-AcCA) was shown as an effective inhibitor of BuChE (IC_50 = 0.5 ± 0.2 μM) and also had a great selectivity for BuChE over AChE (more than 800 fold). Inhibition kinetic study indicated that 11 is a mixed inhibition type. Its binding affinity (Ki) value to BuChE is 1.52 ± 0.18 μM. KCI Citation Count: 13
doi_str_mv 10.5012/bkcs.2011.32.8.2997
format article
fullrecord <record><control><sourceid>nrf_cross</sourceid><recordid>TN_cdi_nrf_kci_oai_kci_go_kr_ARTI_808910</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>oai_kci_go_kr_ARTI_808910</sourcerecordid><originalsourceid>FETCH-LOGICAL-c327t-e01752c08669a168595409d3e73a529c592f898a5f4e52b1e548b573b3e6bab23</originalsourceid><addsrcrecordid>eNotkLtOwzAUQC0EEuXxBSweYUiwr-PEHkt5VSoClTJbiXtDTdI4sgNS_h4CTGc5OsMh5IKzVDIO11VjYwqM81RAqlLQujggMw6gE6kzfUhmDKRIQOfZMTmJ8YMxKAqQM9Lc4he2vt9jN1Bf01ds0Q7uC-nN5zCGsbU737oO44ChjEiX3c5VbvAh0rfound6ub5KVq73ztK5ddvkxbdjv8POt_RxrILb0if_k_xsMZ6Ro7psI57_85S83d9tFo_J6vlhuZivEiugGBJkvJBgmcpzXfJcSS0zprcCC1FK0FZqqJVWpawzlFBxlJmqZCEqgXlVViBOyeVftwu1aawzvnS_fPemCWa-3iyNYkpz9qOKP9UGH2PA2vTB7cswGs7MtNZMa8201ggwykxrxTcfX24s</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Development of Selective Butyrylcholinesterase Inhibitors Using (R)-Lipoic Acid-Polyphenol Hybrid Molecules</title><source>Free Full-Text Journals in Chemistry</source><creator>Woo, Yeun-Ji ; Lee, Bo-Hyun ; Yeun, Go-Heum ; Kim, Hyun-Ju ; Ko, Jang-Myoun ; Won, Moo-Ho ; Lee, Bong-Ho ; Park, Jeong-Ho</creator><creatorcontrib>Woo, Yeun-Ji ; Lee, Bo-Hyun ; Yeun, Go-Heum ; Kim, Hyun-Ju ; Ko, Jang-Myoun ; Won, Moo-Ho ; Lee, Bong-Ho ; Park, Jeong-Ho</creatorcontrib><description>A series of hybrid molecules between (R)-lipoic acid (ALA) and the acetylated or methylated polyphenol compounds were synthesized and their in vitro cholinesterase [acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE)] inhibition activities were checked. The IC_50 values of all hybrid molecules for a BuChE inhibition were lower than those of the single parent compounds. Specifically, ALA-acetyl protected caffeic acid (11,ALA-AcCA) was shown as an effective inhibitor of BuChE (IC_50 = 0.5 ± 0.2 μM) and also had a great selectivity for BuChE over AChE (more than 800 fold). Inhibition kinetic study indicated that 11 is a mixed inhibition type. Its binding affinity (Ki) value to BuChE is 1.52 ± 0.18 μM. KCI Citation Count: 13</description><identifier>ISSN: 0253-2964</identifier><identifier>EISSN: 1229-5949</identifier><identifier>DOI: 10.5012/bkcs.2011.32.8.2997</identifier><language>eng</language><publisher>대한화학회</publisher><subject>화학</subject><ispartof>Bulletin of the Korean Chemical Society, 2011, 32(8), , pp.2997-3002</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c327t-e01752c08669a168595409d3e73a529c592f898a5f4e52b1e548b573b3e6bab23</citedby><cites>FETCH-LOGICAL-c327t-e01752c08669a168595409d3e73a529c592f898a5f4e52b1e548b573b3e6bab23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001576709$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Woo, Yeun-Ji</creatorcontrib><creatorcontrib>Lee, Bo-Hyun</creatorcontrib><creatorcontrib>Yeun, Go-Heum</creatorcontrib><creatorcontrib>Kim, Hyun-Ju</creatorcontrib><creatorcontrib>Ko, Jang-Myoun</creatorcontrib><creatorcontrib>Won, Moo-Ho</creatorcontrib><creatorcontrib>Lee, Bong-Ho</creatorcontrib><creatorcontrib>Park, Jeong-Ho</creatorcontrib><title>Development of Selective Butyrylcholinesterase Inhibitors Using (R)-Lipoic Acid-Polyphenol Hybrid Molecules</title><title>Bulletin of the Korean Chemical Society</title><description>A series of hybrid molecules between (R)-lipoic acid (ALA) and the acetylated or methylated polyphenol compounds were synthesized and their in vitro cholinesterase [acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE)] inhibition activities were checked. The IC_50 values of all hybrid molecules for a BuChE inhibition were lower than those of the single parent compounds. Specifically, ALA-acetyl protected caffeic acid (11,ALA-AcCA) was shown as an effective inhibitor of BuChE (IC_50 = 0.5 ± 0.2 μM) and also had a great selectivity for BuChE over AChE (more than 800 fold). Inhibition kinetic study indicated that 11 is a mixed inhibition type. Its binding affinity (Ki) value to BuChE is 1.52 ± 0.18 μM. KCI Citation Count: 13</description><subject>화학</subject><issn>0253-2964</issn><issn>1229-5949</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNotkLtOwzAUQC0EEuXxBSweYUiwr-PEHkt5VSoClTJbiXtDTdI4sgNS_h4CTGc5OsMh5IKzVDIO11VjYwqM81RAqlLQujggMw6gE6kzfUhmDKRIQOfZMTmJ8YMxKAqQM9Lc4he2vt9jN1Bf01ds0Q7uC-nN5zCGsbU737oO44ChjEiX3c5VbvAh0rfound6ub5KVq73ztK5ddvkxbdjv8POt_RxrILb0if_k_xsMZ6Ro7psI57_85S83d9tFo_J6vlhuZivEiugGBJkvJBgmcpzXfJcSS0zprcCC1FK0FZqqJVWpawzlFBxlJmqZCEqgXlVViBOyeVftwu1aawzvnS_fPemCWa-3iyNYkpz9qOKP9UGH2PA2vTB7cswGs7MtNZMa8201ggwykxrxTcfX24s</recordid><startdate>20110820</startdate><enddate>20110820</enddate><creator>Woo, Yeun-Ji</creator><creator>Lee, Bo-Hyun</creator><creator>Yeun, Go-Heum</creator><creator>Kim, Hyun-Ju</creator><creator>Ko, Jang-Myoun</creator><creator>Won, Moo-Ho</creator><creator>Lee, Bong-Ho</creator><creator>Park, Jeong-Ho</creator><general>대한화학회</general><scope>AAYXX</scope><scope>CITATION</scope><scope>ACYCR</scope></search><sort><creationdate>20110820</creationdate><title>Development of Selective Butyrylcholinesterase Inhibitors Using (R)-Lipoic Acid-Polyphenol Hybrid Molecules</title><author>Woo, Yeun-Ji ; Lee, Bo-Hyun ; Yeun, Go-Heum ; Kim, Hyun-Ju ; Ko, Jang-Myoun ; Won, Moo-Ho ; Lee, Bong-Ho ; Park, Jeong-Ho</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c327t-e01752c08669a168595409d3e73a529c592f898a5f4e52b1e548b573b3e6bab23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>화학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Woo, Yeun-Ji</creatorcontrib><creatorcontrib>Lee, Bo-Hyun</creatorcontrib><creatorcontrib>Yeun, Go-Heum</creatorcontrib><creatorcontrib>Kim, Hyun-Ju</creatorcontrib><creatorcontrib>Ko, Jang-Myoun</creatorcontrib><creatorcontrib>Won, Moo-Ho</creatorcontrib><creatorcontrib>Lee, Bong-Ho</creatorcontrib><creatorcontrib>Park, Jeong-Ho</creatorcontrib><collection>CrossRef</collection><collection>Korean Citation Index</collection><jtitle>Bulletin of the Korean Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Woo, Yeun-Ji</au><au>Lee, Bo-Hyun</au><au>Yeun, Go-Heum</au><au>Kim, Hyun-Ju</au><au>Ko, Jang-Myoun</au><au>Won, Moo-Ho</au><au>Lee, Bong-Ho</au><au>Park, Jeong-Ho</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of Selective Butyrylcholinesterase Inhibitors Using (R)-Lipoic Acid-Polyphenol Hybrid Molecules</atitle><jtitle>Bulletin of the Korean Chemical Society</jtitle><date>2011-08-20</date><risdate>2011</risdate><volume>32</volume><issue>spc8</issue><spage>2997</spage><epage>3002</epage><pages>2997-3002</pages><issn>0253-2964</issn><eissn>1229-5949</eissn><abstract>A series of hybrid molecules between (R)-lipoic acid (ALA) and the acetylated or methylated polyphenol compounds were synthesized and their in vitro cholinesterase [acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE)] inhibition activities were checked. The IC_50 values of all hybrid molecules for a BuChE inhibition were lower than those of the single parent compounds. Specifically, ALA-acetyl protected caffeic acid (11,ALA-AcCA) was shown as an effective inhibitor of BuChE (IC_50 = 0.5 ± 0.2 μM) and also had a great selectivity for BuChE over AChE (more than 800 fold). Inhibition kinetic study indicated that 11 is a mixed inhibition type. Its binding affinity (Ki) value to BuChE is 1.52 ± 0.18 μM. KCI Citation Count: 13</abstract><pub>대한화학회</pub><doi>10.5012/bkcs.2011.32.8.2997</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0253-2964
ispartof Bulletin of the Korean Chemical Society, 2011, 32(8), , pp.2997-3002
issn 0253-2964
1229-5949
language eng
recordid cdi_nrf_kci_oai_kci_go_kr_ARTI_808910
source Free Full-Text Journals in Chemistry
subjects 화학
title Development of Selective Butyrylcholinesterase Inhibitors Using (R)-Lipoic Acid-Polyphenol Hybrid Molecules
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T12%3A50%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-nrf_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Development%20of%20Selective%20Butyrylcholinesterase%20Inhibitors%20Using%20(R)-Lipoic%20Acid-Polyphenol%20Hybrid%20Molecules&rft.jtitle=Bulletin%20of%20the%20Korean%20Chemical%20Society&rft.au=Woo,%20Yeun-Ji&rft.date=2011-08-20&rft.volume=32&rft.issue=spc8&rft.spage=2997&rft.epage=3002&rft.pages=2997-3002&rft.issn=0253-2964&rft.eissn=1229-5949&rft_id=info:doi/10.5012/bkcs.2011.32.8.2997&rft_dat=%3Cnrf_cross%3Eoai_kci_go_kr_ARTI_808910%3C/nrf_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c327t-e01752c08669a168595409d3e73a529c592f898a5f4e52b1e548b573b3e6bab23%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true