Structure–activity relationship of benzoxazinones and related compounds with respect to the growth inhibition and α-amylase activity in cress seedlings

Benzoxazinones and their degradation compounds inhibited root growth and α-amylase activity in cress seedlings. The inhibitory activity of these compounds was divided into three groups: the high active group; 2,4-dihydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, 2,4-dihydroxy-(2H)-1,4-benzoxazin-3(...

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Veröffentlicht in:Journal of plant physiology 2010-01, Vol.167 (15), p.1221-1225
Hauptverfasser: Kato-Noguchi, Hisashi, Macías, Francisco A, Molinillo, José M.G
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Macías, Francisco A
Molinillo, José M.G
description Benzoxazinones and their degradation compounds inhibited root growth and α-amylase activity in cress seedlings. The inhibitory activity of these compounds was divided into three groups: the high active group; 2,4-dihydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, 2,4-dihydroxy-(2H)-1,4-benzoxazin-3(4H)-one, 4-hydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, 4-hydroxy-(2H)-1,4-benzoxazin-3(4H)-one, the moderate active group; 7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, (2H)-1,4-benzoxazin-3(4H)-one, 6-methoxy-benzoxazolin-2(3H)-one, benzoxazolin-2(3H)-one and 2-amino-phenoxazine-3-one, and the low active group; 2-hydroxy-(2H)-1,4-benzoxazin-3(4H)-one, 2-hydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, 2-amino-7-hydroxyphenoxazine-3-one and 2-amino-7-methoxyphenoxazine-3-one. The structure–activity of these compounds suggests that compounds that have benzoxazinone skeletons are the most active structure, and a hydroxyl group at position C-2 on the benzoxazinone skeleton may not affect inhibitory activity, whereas a hydroxyl group at position N-4 on the skeleton is essential for inhibitory activity. However, the concentration–response curves of these compounds and the I50 values (the concentrations required for 50% inhibition) for root growth and α-amylase indicated that root growth was positively correlated with the α-amylase activity in the seedlings. α-Amylase is required not only for seed germination, but also subsequent seedling growth until photosynthesis is sufficient to support seedling growth. Therefore, these results suggest that the compounds studied here may inhibit the root growth of cress seedlings by inhibiting α-amylase activity.
doi_str_mv 10.1016/j.jplph.2010.04.006
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The inhibitory activity of these compounds was divided into three groups: the high active group; 2,4-dihydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, 2,4-dihydroxy-(2H)-1,4-benzoxazin-3(4H)-one, 4-hydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, 4-hydroxy-(2H)-1,4-benzoxazin-3(4H)-one, the moderate active group; 7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, (2H)-1,4-benzoxazin-3(4H)-one, 6-methoxy-benzoxazolin-2(3H)-one, benzoxazolin-2(3H)-one and 2-amino-phenoxazine-3-one, and the low active group; 2-hydroxy-(2H)-1,4-benzoxazin-3(4H)-one, 2-hydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, 2-amino-7-hydroxyphenoxazine-3-one and 2-amino-7-methoxyphenoxazine-3-one. The structure–activity of these compounds suggests that compounds that have benzoxazinone skeletons are the most active structure, and a hydroxyl group at position C-2 on the benzoxazinone skeleton may not affect inhibitory activity, whereas a hydroxyl group at position N-4 on the skeleton is essential for inhibitory activity. However, the concentration–response curves of these compounds and the I50 values (the concentrations required for 50% inhibition) for root growth and α-amylase indicated that root growth was positively correlated with the α-amylase activity in the seedlings. α-Amylase is required not only for seed germination, but also subsequent seedling growth until photosynthesis is sufficient to support seedling growth. 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Psychology ; Growth inhibitor ; Lepidium sativum ; Plant physiology and development ; Plant Roots - drug effects ; Plant Roots - enzymology ; Plant Roots - growth &amp; development ; root growth ; seed germination ; seedling growth ; seedlings ; Seedlings - drug effects ; Seedlings - enzymology ; Seedlings - growth &amp; development ; Structure-Activity Relationship ; α-Amylase</subject><ispartof>Journal of plant physiology, 2010-01, Vol.167 (15), p.1221-1225</ispartof><rights>2010 Elsevier GmbH</rights><rights>2015 INIST-CNRS</rights><rights>Copyright (c) 2010 Elsevier GmbH. 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The inhibitory activity of these compounds was divided into three groups: the high active group; 2,4-dihydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, 2,4-dihydroxy-(2H)-1,4-benzoxazin-3(4H)-one, 4-hydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, 4-hydroxy-(2H)-1,4-benzoxazin-3(4H)-one, the moderate active group; 7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, (2H)-1,4-benzoxazin-3(4H)-one, 6-methoxy-benzoxazolin-2(3H)-one, benzoxazolin-2(3H)-one and 2-amino-phenoxazine-3-one, and the low active group; 2-hydroxy-(2H)-1,4-benzoxazin-3(4H)-one, 2-hydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, 2-amino-7-hydroxyphenoxazine-3-one and 2-amino-7-methoxyphenoxazine-3-one. The structure–activity of these compounds suggests that compounds that have benzoxazinone skeletons are the most active structure, and a hydroxyl group at position C-2 on the benzoxazinone skeleton may not affect inhibitory activity, whereas a hydroxyl group at position N-4 on the skeleton is essential for inhibitory activity. However, the concentration–response curves of these compounds and the I50 values (the concentrations required for 50% inhibition) for root growth and α-amylase indicated that root growth was positively correlated with the α-amylase activity in the seedlings. α-Amylase is required not only for seed germination, but also subsequent seedling growth until photosynthesis is sufficient to support seedling growth. Therefore, these results suggest that the compounds studied here may inhibit the root growth of cress seedlings by inhibiting α-amylase activity.</description><subject>alpha-amylase</subject><subject>alpha-Amylases - metabolism</subject><subject>Aminophenoxazine</subject><subject>Benzoxazines - chemistry</subject><subject>Benzoxazines - pharmacology</subject><subject>benzoxazinoids</subject><subject>Benzoxazinone</subject><subject>Benzoxazolinone</subject><subject>Biological and medical sciences</subject><subject>Brassicaceae</subject><subject>Brassicaceae - drug effects</subject><subject>Brassicaceae - enzymology</subject><subject>Brassicaceae - growth &amp; development</subject><subject>correlation</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Growth inhibitor</subject><subject>Lepidium sativum</subject><subject>Plant physiology and development</subject><subject>Plant Roots - drug effects</subject><subject>Plant Roots - enzymology</subject><subject>Plant Roots - growth &amp; development</subject><subject>root growth</subject><subject>seed germination</subject><subject>seedling growth</subject><subject>seedlings</subject><subject>Seedlings - drug effects</subject><subject>Seedlings - enzymology</subject><subject>Seedlings - growth &amp; development</subject><subject>Structure-Activity Relationship</subject><subject>α-Amylase</subject><issn>0176-1617</issn><issn>1618-1328</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kkFu1DAYhS0EokPhBEjgDWKVwY4TJ1mwqCoKSJVYlK4tx_4z8Sixg-20TFfcoTtuwUU4BCfB0wxlBSvLT997v34_I_SckjUllL_ZrrfTMPXrnCSFFGtC-AO0opzWGWV5_RCtCK14loTqCD0JYUvSvazZY3SUE05KXrIV-n4R_azi7OHXt1uporkycYc9DDIaZ0NvJuw63IK9cV_ljbHOQsDS6gUBjZUbJzdbHfC1iX2SwwQq4uhw7AFvvLtOqrG9ac0-8c7780cmx90gA-D7kcZilcwBBwA9GLsJT9GjTg4Bnh3OY3R59u7z6Yfs_NP7j6cn55kqGI9ZrRsApqAotapoUygl6yJnum0qyhkvKWkkJapiXS5Vp9siLV6xkgNnTDKl2DF6veRO3n2ZIUQxmqBgGKQFNwdRFXVTlxVliWQLqbwLwUMnJm9G6XeCErHvRGzFXSdi34kghUidJNeLQ_7cjqDvPX9KSMCrAyCDkkPnpVUm_OVYnuesahL3cuE66YTc-MRcXqRJBUljaFGTfxKM0LpOn4Em4u1CQHrRKwNeBGXAKtDGp96Edua_y_wG-OTDpg</recordid><startdate>20100101</startdate><enddate>20100101</enddate><creator>Kato-Noguchi, Hisashi</creator><creator>Macías, Francisco A</creator><creator>Molinillo, José M.G</creator><general>Elsevier GmbH</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20100101</creationdate><title>Structure–activity relationship of benzoxazinones and related compounds with respect to the growth inhibition and α-amylase activity in cress seedlings</title><author>Kato-Noguchi, Hisashi ; Macías, Francisco A ; Molinillo, José M.G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-8d9ee3ce45dc7194cca8423db9716365109a10c73f2acfdb45657356e633a3cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>alpha-amylase</topic><topic>alpha-Amylases - metabolism</topic><topic>Aminophenoxazine</topic><topic>Benzoxazines - chemistry</topic><topic>Benzoxazines - pharmacology</topic><topic>benzoxazinoids</topic><topic>Benzoxazinone</topic><topic>Benzoxazolinone</topic><topic>Biological and medical sciences</topic><topic>Brassicaceae</topic><topic>Brassicaceae - drug effects</topic><topic>Brassicaceae - enzymology</topic><topic>Brassicaceae - growth &amp; development</topic><topic>correlation</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Growth inhibitor</topic><topic>Lepidium sativum</topic><topic>Plant physiology and development</topic><topic>Plant Roots - drug effects</topic><topic>Plant Roots - enzymology</topic><topic>Plant Roots - growth &amp; development</topic><topic>root growth</topic><topic>seed germination</topic><topic>seedling growth</topic><topic>seedlings</topic><topic>Seedlings - drug effects</topic><topic>Seedlings - enzymology</topic><topic>Seedlings - growth &amp; development</topic><topic>Structure-Activity Relationship</topic><topic>α-Amylase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kato-Noguchi, Hisashi</creatorcontrib><creatorcontrib>Macías, Francisco A</creatorcontrib><creatorcontrib>Molinillo, José M.G</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of plant physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kato-Noguchi, Hisashi</au><au>Macías, Francisco A</au><au>Molinillo, José M.G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structure–activity relationship of benzoxazinones and related compounds with respect to the growth inhibition and α-amylase activity in cress seedlings</atitle><jtitle>Journal of plant physiology</jtitle><addtitle>J Plant Physiol</addtitle><date>2010-01-01</date><risdate>2010</risdate><volume>167</volume><issue>15</issue><spage>1221</spage><epage>1225</epage><pages>1221-1225</pages><issn>0176-1617</issn><eissn>1618-1328</eissn><coden>JPPHEY</coden><abstract>Benzoxazinones and their degradation compounds inhibited root growth and α-amylase activity in cress seedlings. The inhibitory activity of these compounds was divided into three groups: the high active group; 2,4-dihydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, 2,4-dihydroxy-(2H)-1,4-benzoxazin-3(4H)-one, 4-hydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, 4-hydroxy-(2H)-1,4-benzoxazin-3(4H)-one, the moderate active group; 7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, (2H)-1,4-benzoxazin-3(4H)-one, 6-methoxy-benzoxazolin-2(3H)-one, benzoxazolin-2(3H)-one and 2-amino-phenoxazine-3-one, and the low active group; 2-hydroxy-(2H)-1,4-benzoxazin-3(4H)-one, 2-hydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one, 2-amino-7-hydroxyphenoxazine-3-one and 2-amino-7-methoxyphenoxazine-3-one. The structure–activity of these compounds suggests that compounds that have benzoxazinone skeletons are the most active structure, and a hydroxyl group at position C-2 on the benzoxazinone skeleton may not affect inhibitory activity, whereas a hydroxyl group at position N-4 on the skeleton is essential for inhibitory activity. However, the concentration–response curves of these compounds and the I50 values (the concentrations required for 50% inhibition) for root growth and α-amylase indicated that root growth was positively correlated with the α-amylase activity in the seedlings. α-Amylase is required not only for seed germination, but also subsequent seedling growth until photosynthesis is sufficient to support seedling growth. Therefore, these results suggest that the compounds studied here may inhibit the root growth of cress seedlings by inhibiting α-amylase activity.</abstract><cop>Munich</cop><pub>Elsevier GmbH</pub><pmid>20605653</pmid><doi>10.1016/j.jplph.2010.04.006</doi><tpages>5</tpages></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects alpha-amylase
alpha-Amylases - metabolism
Aminophenoxazine
Benzoxazines - chemistry
Benzoxazines - pharmacology
benzoxazinoids
Benzoxazinone
Benzoxazolinone
Biological and medical sciences
Brassicaceae
Brassicaceae - drug effects
Brassicaceae - enzymology
Brassicaceae - growth & development
correlation
Fundamental and applied biological sciences. Psychology
Growth inhibitor
Lepidium sativum
Plant physiology and development
Plant Roots - drug effects
Plant Roots - enzymology
Plant Roots - growth & development
root growth
seed germination
seedling growth
seedlings
Seedlings - drug effects
Seedlings - enzymology
Seedlings - growth & development
Structure-Activity Relationship
α-Amylase
title Structure–activity relationship of benzoxazinones and related compounds with respect to the growth inhibition and α-amylase activity in cress seedlings
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