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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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. Therefore, these results suggest that the compounds studied here may inhibit the root growth of cress seedlings by inhibiting α-amylase activity.</description><identifier>ISSN: 0176-1617</identifier><identifier>EISSN: 1618-1328</identifier><identifier>DOI: 10.1016/j.jplph.2010.04.006</identifier><identifier>PMID: 20605653</identifier><identifier>CODEN: JPPHEY</identifier><language>eng</language><publisher>Munich: Elsevier GmbH</publisher><subject>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</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. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-8d9ee3ce45dc7194cca8423db9716365109a10c73f2acfdb45657356e633a3cc3</citedby><cites>FETCH-LOGICAL-c436t-8d9ee3ce45dc7194cca8423db9716365109a10c73f2acfdb45657356e633a3cc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0176161710002191$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23222379$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20605653$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kato-Noguchi, Hisashi</creatorcontrib><creatorcontrib>Macías, Francisco A</creatorcontrib><creatorcontrib>Molinillo, José M.G</creatorcontrib><title>Structure–activity relationship of benzoxazinones and related compounds with respect to the growth inhibition and α-amylase activity in cress seedlings</title><title>Journal of plant physiology</title><addtitle>J Plant Physiol</addtitle><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.</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 & 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 & 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 & 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 & 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 & 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 & 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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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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