Loading…

Synthesis and Biological Activities of Ferulic Acid-Amino Acid Derivatives

Three series of ferulic acid derivatives (feruloylaminoacid benzyl ester or methyl ester, feruloylaminoacid, and 4-O-[N-carbobenzyloxy)-aminoacyl]ferulic acid) were synthesized newly, and their superoxide dismutase (SOD)-like, platelet aggregation (PA)-in-hibitory, tyrosinase-inhibitory,, and angiot...

Full description

Saved in:
Bibliographic Details
Published in:Bioscience, biotechnology, and biochemistry biotechnology, and biochemistry, 1997, Vol.61 (3), p.527-529
Main Authors: Miao, Zhuang, Kayahara, Hiroshi, Tadasa, Koji
Format: Article
Language:English
Subjects:
Citations: 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-c560t-6e2e78093a6d4579592deba54db67ab148f907d728fdf4756b422f91e241377a3
cites
container_end_page 529
container_issue 3
container_start_page 527
container_title Bioscience, biotechnology, and biochemistry
container_volume 61
creator Miao, Zhuang
Kayahara, Hiroshi
Tadasa, Koji
description Three series of ferulic acid derivatives (feruloylaminoacid benzyl ester or methyl ester, feruloylaminoacid, and 4-O-[N-carbobenzyloxy)-aminoacyl]ferulic acid) were synthesized newly, and their superoxide dismutase (SOD)-like, platelet aggregation (PA)-in-hibitory, tyrosinase-inhibitory,, and angiotensin converting enzyme (ACE)-inhibitory activities were evaluated. 4-O-[N-(Carbobenzyloxy)isoleucyl]ferulic acid (20) and 4-O-[N-(carbobenzyloxy)prolyl]ferulic acid (21) showed potent PA-inhibitory activities and tyrosinase-inhibitory activities, while they also had SOD-like activities at the same level as ferulic acid.
doi_str_mv 10.1271/bbb.61.527
format article
fullrecord <record><control><sourceid>proquest_pasca</sourceid><recordid>TN_cdi_proquest_journals_1449426052</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3121796871</sourcerecordid><originalsourceid>FETCH-LOGICAL-c560t-6e2e78093a6d4579592deba54db67ab148f907d728fdf4756b422f91e241377a3</originalsourceid><addsrcrecordid>eNptkEtLAzEUhYMoWKsbf8GAroSpSSaPybJW64OCC3UdkkmiKdNJTaaV_ntTW125upfDd87lHgDOERwhzNG11nrE0IhifgAGqCK8ZILwQzCAArGyJhQdg5OU5hBmgaIBeHrZdP2HTT4VqjPFjQ9tePeNaotx0_u1771NRXDF1MZV65uselOOF74LP2txa6Nfq0zadAqOnGqTPdvPIXib3r1OHsrZ8_3jZDwrG8pgXzKLLa-hqBQzhHJBBTZWK0qMZlxpRGonIDcc1844winTBGMnkMUEVZyraggudrnLGD5XNvVyHlaxyyclIkQQzCDFmbraUU0MKUXr5DL6hYobiaDcdiVzV5IhmbvK8OU-UqX8u4uqa3z6c2DGGRbbTLrDfOdCXKivEFsje7VpQ_z1VP_EfwN_n3nx</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1449426052</pqid></control><display><type>article</type><title>Synthesis and Biological Activities of Ferulic Acid-Amino Acid Derivatives</title><source>Oxford Journals Online</source><source>EZB Electronic Journals Library</source><creator>Miao, Zhuang ; Kayahara, Hiroshi ; Tadasa, Koji</creator><creatorcontrib>Miao, Zhuang ; Kayahara, Hiroshi ; Tadasa, Koji</creatorcontrib><description>Three series of ferulic acid derivatives (feruloylaminoacid benzyl ester or methyl ester, feruloylaminoacid, and 4-O-[N-carbobenzyloxy)-aminoacyl]ferulic acid) were synthesized newly, and their superoxide dismutase (SOD)-like, platelet aggregation (PA)-in-hibitory, tyrosinase-inhibitory,, and angiotensin converting enzyme (ACE)-inhibitory activities were evaluated. 4-O-[N-(Carbobenzyloxy)isoleucyl]ferulic acid (20) and 4-O-[N-(carbobenzyloxy)prolyl]ferulic acid (21) showed potent PA-inhibitory activities and tyrosinase-inhibitory activities, while they also had SOD-like activities at the same level as ferulic acid.</description><identifier>ISSN: 0916-8451</identifier><identifier>EISSN: 1347-6947</identifier><identifier>DOI: 10.1271/bbb.61.527</identifier><language>eng</language><publisher>Tokyo: Taylor &amp; Francis</publisher><subject>angiotensin converting enzyme ; Biological and medical sciences ; Blood. Blood coagulation. Reticuloendothelial system ; ferulic acid-amino acid derivatives ; Medical sciences ; Pharmacology. Drug treatments ; platelet aggregation ; superoxide radical ; tyrosinase</subject><ispartof>Bioscience, biotechnology, and biochemistry, 1997, Vol.61 (3), p.527-529</ispartof><rights>Copyright 1997 Taylor and Francis Group LLC 1997</rights><rights>1997 INIST-CNRS</rights><rights>Copyright Japan Science and Technology Agency 1997</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c560t-6e2e78093a6d4579592deba54db67ab148f907d728fdf4756b422f91e241377a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=2676292$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Miao, Zhuang</creatorcontrib><creatorcontrib>Kayahara, Hiroshi</creatorcontrib><creatorcontrib>Tadasa, Koji</creatorcontrib><title>Synthesis and Biological Activities of Ferulic Acid-Amino Acid Derivatives</title><title>Bioscience, biotechnology, and biochemistry</title><description>Three series of ferulic acid derivatives (feruloylaminoacid benzyl ester or methyl ester, feruloylaminoacid, and 4-O-[N-carbobenzyloxy)-aminoacyl]ferulic acid) were synthesized newly, and their superoxide dismutase (SOD)-like, platelet aggregation (PA)-in-hibitory, tyrosinase-inhibitory,, and angiotensin converting enzyme (ACE)-inhibitory activities were evaluated. 4-O-[N-(Carbobenzyloxy)isoleucyl]ferulic acid (20) and 4-O-[N-(carbobenzyloxy)prolyl]ferulic acid (21) showed potent PA-inhibitory activities and tyrosinase-inhibitory activities, while they also had SOD-like activities at the same level as ferulic acid.</description><subject>angiotensin converting enzyme</subject><subject>Biological and medical sciences</subject><subject>Blood. Blood coagulation. Reticuloendothelial system</subject><subject>ferulic acid-amino acid derivatives</subject><subject>Medical sciences</subject><subject>Pharmacology. Drug treatments</subject><subject>platelet aggregation</subject><subject>superoxide radical</subject><subject>tyrosinase</subject><issn>0916-8451</issn><issn>1347-6947</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNptkEtLAzEUhYMoWKsbf8GAroSpSSaPybJW64OCC3UdkkmiKdNJTaaV_ntTW125upfDd87lHgDOERwhzNG11nrE0IhifgAGqCK8ZILwQzCAArGyJhQdg5OU5hBmgaIBeHrZdP2HTT4VqjPFjQ9tePeNaotx0_u1771NRXDF1MZV65uselOOF74LP2txa6Nfq0zadAqOnGqTPdvPIXib3r1OHsrZ8_3jZDwrG8pgXzKLLa-hqBQzhHJBBTZWK0qMZlxpRGonIDcc1844winTBGMnkMUEVZyraggudrnLGD5XNvVyHlaxyyclIkQQzCDFmbraUU0MKUXr5DL6hYobiaDcdiVzV5IhmbvK8OU-UqX8u4uqa3z6c2DGGRbbTLrDfOdCXKivEFsje7VpQ_z1VP_EfwN_n3nx</recordid><startdate>1997</startdate><enddate>1997</enddate><creator>Miao, Zhuang</creator><creator>Kayahara, Hiroshi</creator><creator>Tadasa, Koji</creator><general>Taylor &amp; Francis</general><general>Japan Society for Bioscience Biotechnology and Agrochemistry</general><general>Oxford University Press</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>1997</creationdate><title>Synthesis and Biological Activities of Ferulic Acid-Amino Acid Derivatives</title><author>Miao, Zhuang ; Kayahara, Hiroshi ; Tadasa, Koji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c560t-6e2e78093a6d4579592deba54db67ab148f907d728fdf4756b422f91e241377a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>angiotensin converting enzyme</topic><topic>Biological and medical sciences</topic><topic>Blood. Blood coagulation. Reticuloendothelial system</topic><topic>ferulic acid-amino acid derivatives</topic><topic>Medical sciences</topic><topic>Pharmacology. Drug treatments</topic><topic>platelet aggregation</topic><topic>superoxide radical</topic><topic>tyrosinase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miao, Zhuang</creatorcontrib><creatorcontrib>Kayahara, Hiroshi</creatorcontrib><creatorcontrib>Tadasa, Koji</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Bioscience, biotechnology, and biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miao, Zhuang</au><au>Kayahara, Hiroshi</au><au>Tadasa, Koji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Biological Activities of Ferulic Acid-Amino Acid Derivatives</atitle><jtitle>Bioscience, biotechnology, and biochemistry</jtitle><date>1997</date><risdate>1997</risdate><volume>61</volume><issue>3</issue><spage>527</spage><epage>529</epage><pages>527-529</pages><issn>0916-8451</issn><eissn>1347-6947</eissn><abstract>Three series of ferulic acid derivatives (feruloylaminoacid benzyl ester or methyl ester, feruloylaminoacid, and 4-O-[N-carbobenzyloxy)-aminoacyl]ferulic acid) were synthesized newly, and their superoxide dismutase (SOD)-like, platelet aggregation (PA)-in-hibitory, tyrosinase-inhibitory,, and angiotensin converting enzyme (ACE)-inhibitory activities were evaluated. 4-O-[N-(Carbobenzyloxy)isoleucyl]ferulic acid (20) and 4-O-[N-(carbobenzyloxy)prolyl]ferulic acid (21) showed potent PA-inhibitory activities and tyrosinase-inhibitory activities, while they also had SOD-like activities at the same level as ferulic acid.</abstract><cop>Tokyo</cop><pub>Taylor &amp; Francis</pub><doi>10.1271/bbb.61.527</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0916-8451
ispartof Bioscience, biotechnology, and biochemistry, 1997, Vol.61 (3), p.527-529
issn 0916-8451
1347-6947
language eng
recordid cdi_proquest_journals_1449426052
source Oxford Journals Online; EZB Electronic Journals Library
subjects angiotensin converting enzyme
Biological and medical sciences
Blood. Blood coagulation. Reticuloendothelial system
ferulic acid-amino acid derivatives
Medical sciences
Pharmacology. Drug treatments
platelet aggregation
superoxide radical
tyrosinase
title Synthesis and Biological Activities of Ferulic Acid-Amino Acid Derivatives
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T01%3A52%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pasca&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20and%20Biological%20Activities%20of%20Ferulic%20Acid-Amino%20Acid%20Derivatives&rft.jtitle=Bioscience,%20biotechnology,%20and%20biochemistry&rft.au=Miao,%20Zhuang&rft.date=1997&rft.volume=61&rft.issue=3&rft.spage=527&rft.epage=529&rft.pages=527-529&rft.issn=0916-8451&rft.eissn=1347-6947&rft_id=info:doi/10.1271/bbb.61.527&rft_dat=%3Cproquest_pasca%3E3121796871%3C/proquest_pasca%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c560t-6e2e78093a6d4579592deba54db67ab148f907d728fdf4756b422f91e241377a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1449426052&rft_id=info:pmid/&rfr_iscdi=true