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N-Alkylaryltriazine Herbicides: A Possible Link Between Triazines and Phenylureas
A comparison of the structure of the α-methylbenzyl analogue (MBAT) of atrazine with the Photosystem II herbicides atrazine [6-chloro-N-ethyl-N′-(1-methylethyl)-1,3,5-triazine-2,4-diamine] and diuron [N′-(3,4-dichlorophenyl)-N,N-dimethylurea] suggested that N-alkylbenzyltriazines may be a structural...
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Published in: | Weed science 1987-11, Vol.35 (6), p.763-769 |
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container_title | Weed science |
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creator | Gardner, Gary Sanborn, James R. Goss, John R. |
description | A comparison of the structure of the α-methylbenzyl analogue (MBAT) of atrazine with the Photosystem II herbicides atrazine [6-chloro-N-ethyl-N′-(1-methylethyl)-1,3,5-triazine-2,4-diamine] and diuron [N′-(3,4-dichlorophenyl)-N,N-dimethylurea] suggested that N-alkylbenzyltriazines may be a structural bridge between the triazines and the phenylureas. In the phenylureas, the addition of chlorines at the meta and/or para positions produces a marked increase in activity. Chloro-substituted derivatives of MBAT were synthesized to determine whether this structure-activity relationship also applies to the alkylaryltriazines. Addition of a chlorine to MBAT at the 4-position (CMBAT) caused a substantial increase in intrinsic activity, and a second chlorine at the 3-position (DCMBAT) caused a further increase. In direct comparisons, DCMBAT was more active in vitro than terbuthylazine [6-chloro-N-ethyl-N′-(1,1-dimethylethyl)-1,3,5-triazine-2,4-diamine], the most active chlorotriazine, and was also more active than diruon. The effects of DCMBAT were also measured on triazine-resistant pigweed (Amaranthus hybridus L. # AMACH) both in vivo and in vitro. The activity of this compound in triazine-resistant chloroplasts was intermediate between that of atrazine and diruon both in inhibition of photosynthetic electron transport and in competition for diuron binding sites, with half-maximal values falling in the micromolar range. Whole plant phytotoxicity of DCMBAT on triazine-resistant pigweed was also intermediate between that of diuron and atrazine. Since DCMBAT is a triazine with biological properties similar to that of a urea, we conclude that in a functional as well as structural sense, DCMBAT is a herbicide that is a hybrid between a triazine and a urea. |
doi_str_mv | 10.1017/S0043174500079303 |
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In the phenylureas, the addition of chlorines at the meta and/or para positions produces a marked increase in activity. Chloro-substituted derivatives of MBAT were synthesized to determine whether this structure-activity relationship also applies to the alkylaryltriazines. Addition of a chlorine to MBAT at the 4-position (CMBAT) caused a substantial increase in intrinsic activity, and a second chlorine at the 3-position (DCMBAT) caused a further increase. In direct comparisons, DCMBAT was more active in vitro than terbuthylazine [6-chloro-N-ethyl-N′-(1,1-dimethylethyl)-1,3,5-triazine-2,4-diamine], the most active chlorotriazine, and was also more active than diruon. The effects of DCMBAT were also measured on triazine-resistant pigweed (Amaranthus hybridus L. # AMACH) both in vivo and in vitro. The activity of this compound in triazine-resistant chloroplasts was intermediate between that of atrazine and diruon both in inhibition of photosynthetic electron transport and in competition for diuron binding sites, with half-maximal values falling in the micromolar range. Whole plant phytotoxicity of DCMBAT on triazine-resistant pigweed was also intermediate between that of diuron and atrazine. Since DCMBAT is a triazine with biological properties similar to that of a urea, we conclude that in a functional as well as structural sense, DCMBAT is a herbicide that is a hybrid between a triazine and a urea.</description><identifier>ISSN: 0043-1745</identifier><identifier>EISSN: 1550-2759</identifier><identifier>DOI: 10.1017/S0043174500079303</identifier><language>eng</language><publisher>Cambridge, UK: Cambridge University Press</publisher><subject>AMARANTHUS ; AMARANTHUS HYBRIDUS ; AMARANTHUS RETROFLEXUS ; ATRAZINE ; Binding sites ; Chlorine ; Chloroplasts ; DIURON ; Electrons ; HERBICIDAS ; HERBICIDE ; HERBICIDES ; Phenyls ; Photosystem II ; Physiology, Chemistry, and Biochemistry ; Phytotoxicity ; Plants ; Triazines</subject><ispartof>Weed science, 1987-11, Vol.35 (6), p.763-769</ispartof><rights>Copyright © 1987 by the Weed Science Society of America</rights><rights>Copyright 1987 The Weed Science Society of America</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c261t-1cba778d7cde1e60ece6557aa4fecf39668cbb338c1967e8f3f70899c71888543</citedby><cites>FETCH-LOGICAL-c261t-1cba778d7cde1e60ece6557aa4fecf39668cbb338c1967e8f3f70899c71888543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4044567$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4044567$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,58213,58446</link.rule.ids></links><search><creatorcontrib>Gardner, Gary</creatorcontrib><creatorcontrib>Sanborn, James R.</creatorcontrib><creatorcontrib>Goss, John R.</creatorcontrib><title>N-Alkylaryltriazine Herbicides: A Possible Link Between Triazines and Phenylureas</title><title>Weed science</title><addtitle>Weed sci</addtitle><description>A comparison of the structure of the α-methylbenzyl analogue (MBAT) of atrazine with the Photosystem II herbicides atrazine [6-chloro-N-ethyl-N′-(1-methylethyl)-1,3,5-triazine-2,4-diamine] and diuron [N′-(3,4-dichlorophenyl)-N,N-dimethylurea] suggested that N-alkylbenzyltriazines may be a structural bridge between the triazines and the phenylureas. In the phenylureas, the addition of chlorines at the meta and/or para positions produces a marked increase in activity. Chloro-substituted derivatives of MBAT were synthesized to determine whether this structure-activity relationship also applies to the alkylaryltriazines. Addition of a chlorine to MBAT at the 4-position (CMBAT) caused a substantial increase in intrinsic activity, and a second chlorine at the 3-position (DCMBAT) caused a further increase. In direct comparisons, DCMBAT was more active in vitro than terbuthylazine [6-chloro-N-ethyl-N′-(1,1-dimethylethyl)-1,3,5-triazine-2,4-diamine], the most active chlorotriazine, and was also more active than diruon. The effects of DCMBAT were also measured on triazine-resistant pigweed (Amaranthus hybridus L. # AMACH) both in vivo and in vitro. The activity of this compound in triazine-resistant chloroplasts was intermediate between that of atrazine and diruon both in inhibition of photosynthetic electron transport and in competition for diuron binding sites, with half-maximal values falling in the micromolar range. Whole plant phytotoxicity of DCMBAT on triazine-resistant pigweed was also intermediate between that of diuron and atrazine. Since DCMBAT is a triazine with biological properties similar to that of a urea, we conclude that in a functional as well as structural sense, DCMBAT is a herbicide that is a hybrid between a triazine and a urea.</description><subject>AMARANTHUS</subject><subject>AMARANTHUS HYBRIDUS</subject><subject>AMARANTHUS RETROFLEXUS</subject><subject>ATRAZINE</subject><subject>Binding sites</subject><subject>Chlorine</subject><subject>Chloroplasts</subject><subject>DIURON</subject><subject>Electrons</subject><subject>HERBICIDAS</subject><subject>HERBICIDE</subject><subject>HERBICIDES</subject><subject>Phenyls</subject><subject>Photosystem II</subject><subject>Physiology, Chemistry, and Biochemistry</subject><subject>Phytotoxicity</subject><subject>Plants</subject><subject>Triazines</subject><issn>0043-1745</issn><issn>1550-2759</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><recordid>eNp9kM1OwzAQhC0EEqXwAEgc_AKBdR3_hFtBQJEqKGp7jhxnXdymCbJTofL0pGoFByROe_h2dnaGkEsG1wyYupkCpJypVACAyjjwI9JjQkAyUCI7Jr0dTnb8lJzFuARgcsCyHnl7SYbValuZsK3a4M2Xr5GOMBTe-hLjLR3SSROjLyqkY1-v6B22n4g1nR2WIzV1SSfvWG-rTUATz8mJM1XEi8Psk_njw-x-lIxfn57vh-PEDiRrE2YLo5QulS2RoQS0KIVQxqQOreOZlNoWBefaskwq1I47BTrLrGJaa5HyPmH7uzZ0DwZ0-Ufw6y5HziDfdZL_6aTTXO01y9g24UeQQpoKqX6xM01uFsHHfD7VmkkBnWmH-cHRrIvgywXmy2YT6i7lP57f6SZ1uQ</recordid><startdate>198711</startdate><enddate>198711</enddate><creator>Gardner, Gary</creator><creator>Sanborn, James R.</creator><creator>Goss, John R.</creator><general>Cambridge University Press</general><general>Weed Science Society of America</general><scope>FBQ</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>198711</creationdate><title>N-Alkylaryltriazine Herbicides: A Possible Link Between Triazines and Phenylureas</title><author>Gardner, Gary ; Sanborn, James R. ; Goss, John R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c261t-1cba778d7cde1e60ece6557aa4fecf39668cbb338c1967e8f3f70899c71888543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>AMARANTHUS</topic><topic>AMARANTHUS HYBRIDUS</topic><topic>AMARANTHUS RETROFLEXUS</topic><topic>ATRAZINE</topic><topic>Binding sites</topic><topic>Chlorine</topic><topic>Chloroplasts</topic><topic>DIURON</topic><topic>Electrons</topic><topic>HERBICIDAS</topic><topic>HERBICIDE</topic><topic>HERBICIDES</topic><topic>Phenyls</topic><topic>Photosystem II</topic><topic>Physiology, Chemistry, and Biochemistry</topic><topic>Phytotoxicity</topic><topic>Plants</topic><topic>Triazines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gardner, Gary</creatorcontrib><creatorcontrib>Sanborn, James R.</creatorcontrib><creatorcontrib>Goss, John R.</creatorcontrib><collection>AGRIS</collection><collection>CrossRef</collection><jtitle>Weed science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gardner, Gary</au><au>Sanborn, James R.</au><au>Goss, John R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>N-Alkylaryltriazine Herbicides: A Possible Link Between Triazines and Phenylureas</atitle><jtitle>Weed science</jtitle><addtitle>Weed sci</addtitle><date>1987-11</date><risdate>1987</risdate><volume>35</volume><issue>6</issue><spage>763</spage><epage>769</epage><pages>763-769</pages><issn>0043-1745</issn><eissn>1550-2759</eissn><abstract>A comparison of the structure of the α-methylbenzyl analogue (MBAT) of atrazine with the Photosystem II herbicides atrazine [6-chloro-N-ethyl-N′-(1-methylethyl)-1,3,5-triazine-2,4-diamine] and diuron [N′-(3,4-dichlorophenyl)-N,N-dimethylurea] suggested that N-alkylbenzyltriazines may be a structural bridge between the triazines and the phenylureas. In the phenylureas, the addition of chlorines at the meta and/or para positions produces a marked increase in activity. Chloro-substituted derivatives of MBAT were synthesized to determine whether this structure-activity relationship also applies to the alkylaryltriazines. Addition of a chlorine to MBAT at the 4-position (CMBAT) caused a substantial increase in intrinsic activity, and a second chlorine at the 3-position (DCMBAT) caused a further increase. In direct comparisons, DCMBAT was more active in vitro than terbuthylazine [6-chloro-N-ethyl-N′-(1,1-dimethylethyl)-1,3,5-triazine-2,4-diamine], the most active chlorotriazine, and was also more active than diruon. The effects of DCMBAT were also measured on triazine-resistant pigweed (Amaranthus hybridus L. # AMACH) both in vivo and in vitro. The activity of this compound in triazine-resistant chloroplasts was intermediate between that of atrazine and diruon both in inhibition of photosynthetic electron transport and in competition for diuron binding sites, with half-maximal values falling in the micromolar range. Whole plant phytotoxicity of DCMBAT on triazine-resistant pigweed was also intermediate between that of diuron and atrazine. Since DCMBAT is a triazine with biological properties similar to that of a urea, we conclude that in a functional as well as structural sense, DCMBAT is a herbicide that is a hybrid between a triazine and a urea.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><doi>10.1017/S0043174500079303</doi><tpages>7</tpages></addata></record> |
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subjects | AMARANTHUS AMARANTHUS HYBRIDUS AMARANTHUS RETROFLEXUS ATRAZINE Binding sites Chlorine Chloroplasts DIURON Electrons HERBICIDAS HERBICIDE HERBICIDES Phenyls Photosystem II Physiology, Chemistry, and Biochemistry Phytotoxicity Plants Triazines |
title | N-Alkylaryltriazine Herbicides: A Possible Link Between Triazines and Phenylureas |
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