Acibenzolar-S-methyl (original) (raw)
Acibenzolar-S-methyl is the ISO common name for an organic compound that is used as a fungicide. Unusually, it is not directly toxic to fungi but works by inducing systemic acquired resistance, the natural defence system of plants.
Property | Value |
---|---|
dbo:abstract | Acibenzolar-S-methyl is the ISO common name for an organic compound that is used as a fungicide. Unusually, it is not directly toxic to fungi but works by inducing systemic acquired resistance, the natural defence system of plants. (en) Acibenzolar-S-methyl (Abkürzung BTH) ist eine chemische Verbindung, die als Fungizid verwendet wird. BTH leitet sich von Acibenzolar ab. Der Wirkstoff greift in die Salicylsäure-Synthese ein und führt so zur Auslösung einer systemisch aktivierten Resistenz. Es gilt als unbedenklich für den Verbraucher und wird schon bei Tomaten gegen bakterielle Krankheiten eingesetzt. Bei Weintrauben wiesen Versuche nach, dass BTH behandelte Weintrauben mehr Anthocyane (antioxidative Wirkung vermutet) enthielten als unbehandelte. Nach der Rückstands-Höchstmengenverordnung des Bundesministeriums für Verbraucherschutz dürfen nur 0,02 mg/kg von BTH in Eiern, Fleisch und Milchprodukten vorhanden sein. (de) L'acibenzolar-S-méthyl est une substance active de produit phytosanitaire (ou produit phytopharmaceutique, ou pesticide), qui présente un effet fongicide. Analogue de l’acide salicylique, il appartient à la famille chimique des (BTH). Il s"agit du premier produit développé dans les années 1980 et revendiquant un mode d’action de type stimulateur des défenses naturelles des plantes, plus connu sous le nom de BTH et commercialisé par Syngenta aux États-Unis. (fr) Acibenzolar-S-methyl, een stof die afgeleid is van , is een plantenactivator. Dat wil zeggen dat de stof de natuurlijke weerstand van planten tegen bacteriële en schimmelziekten stimuleert, maar zelf niet actief is tegen die organismen. Het is dus strikt genomen geen fungicide, daar het de schimmels niet vernietigt. De stof wordt ingezet voor de bescherming van planten of zaden van onder meer tarwe, gerst, rijst, tabak, en katoen. De stof heeft daarnaast ook een werking als insecticide. Acibenzolar-S-methyl werd ontwikkeld door Novartis (nu Syngenta), die het in de producten Blockade, BION of Actigard op de markt brengt. (nl) Acibenzolar-S-metile è un composto organico fungicida che agisce attivando nelle piante ospitanti i funghi parassiti una difesa autonoma da essi, grazie ad un aumento nella di alcuni geni, come CAD1, NPR1 e PR2. Si tratta di un derivato metilico dell'. (it) Acibenzolar-S-metil (ASM) é um fungicida do grupo químico dos benzothiadiazoles, que tem sido testado como um indutor de resistência em plantas. Não age diretamente sobre o agente patogénico, tendo antes como objetivo ativar naturalmente as defesas da planta, deixando a mesma menos suscetível a doenças e pragas. Deve ser aplicado de forma preventiva, pois ele vai agir sistemicamente, ou seja, vai circular na seiva ativando a resistência da planta de forma generalizada. (pt) |
dbo:alternativeName | BTH, CGA245704 (en) |
dbo:iupacName | S-Methyl 1,2,3-benzothiadiazole-7-carbothioate (en) |
dbo:thumbnail | wiki-commons:Special:FilePath/S-methyl_benzo(d)(1,2...zole-7-carbothioate_200.svg?width=300 |
dbo:wikiPageExternalLink | https://www.apsnet.org/edcenter/apsnetfeatures/Pages/Fungicides.aspx |
dbo:wikiPageID | 9921194 (xsd:integer) |
dbo:wikiPageLength | 14494 (xsd:nonNegativeInteger) |
dbo:wikiPageRevisionID | 1110158552 (xsd:integer) |
dbo:wikiPageWikiLink | dbr:California dbr:Pathogenesis-related_protein dbr:Benzene dbr:Brand_names dbr:United_States_Environmental_Protection_Agency dbc:Benzothiadiazoles dbc:Fungicides dbr:Salicylic_acid dbr:Ester dbr:Esterase dbr:Organic_compound dbr:Thioester dbr:Pyricularia_oryzae dbr:Fungus dbr:Genes dbr:Fungicide dbr:Trivial_name dbr:European_Food_Safety_Authority dbr:Federal_Insecticide,_Fungicide,_and_Rodenticide_Act dbr:Florida dbr:Food_Quality_Protection_Act dbr:Carboxylic_acid dbr:Diazonium_compound dbr:Pesticide_resistance dbr:Recrystallization_(chemistry) dbr:Rice dbc:Thioesters dbr:International_Organization_for_Standardization dbr:Hydrolysis dbr:LD50 dbr:Switzerland dbr:Syngenta dbr:Codex_Alimentarius dbr:Sodium_nitrite dbr:Methyl_jasmonate dbr:Systemic_acquired_resistance dbr:Heterocyclic dbr:Pesticide_regulation_in_the_United_States dbr:Pesticide dbr:Phloem dbr:Seed_treatment dbr:Hydrochloride_salt dbr:1,2,3-benzothiadiazole dbr:File:Acibenzolar_methyl_ester_synthesis.png |
dbp:imagealtr | Space-filling model of the acibenzolar-S-methyl molecule (en) |
dbp:imagefilel | S-methyl benzothiadiazole-7-carbothioate 200.svg (en) |
dbp:imagefiler | Acibenzolar-S-methyl-3D-spacefill.png (en) |
dbp:imagenamel | Skeletal formula of acibenzolar-S-methyl (en) |
dbp:imagesizel | 121 (xsd:integer) |
dbp:imagesizer | 120 (xsd:integer) |
dbp:name | Acibenzolar-S-methyl (en) |
dbp:othernames | BTH, CGA245704 (en) |
dbp:pin | S-Methyl 1,2,3-benzothiadiazole-7-carbothioate (en) |
dbp:wikiPageUsesTemplate | dbt:Chembox dbt:Chembox_Hazards dbt:Chembox_Identifiers dbt:Chembox_Properties dbt:Cite_journal dbt:Reflist dbt:Cascite dbt:Chembox_Related dbt:Chemboximage dbt:Chemspidercite dbt:Ebicite dbt:Fdacite dbt:GHS07 dbt:GHS09 dbt:H-phrases dbt:P-phrases dbt:Stdinchicite dbt:PPDB |
dcterms:subject | dbc:Benzothiadiazoles dbc:Fungicides dbc:Thioesters |
gold:hypernym | dbr:Fungicide |
rdf:type | owl:Thing dul:ChemicalObject dbo:ChemicalSubstance wikidata:Q11173 yago:WikicatNitrogenHeterocycles yago:WikicatOrganosulfurCompounds yago:WikicatSulfurHeterocycles yago:Abstraction100002137 yago:Chemical114806838 yago:Cognition100023271 yago:Compound105870180 yago:Compound114818238 yago:Concept105835747 yago:Content105809192 yago:HeterocyclicCompound115025397 yago:Idea105833840 yago:Ketone114926294 yago:Material114580897 yago:Matter100020827 yago:OrganicCompound114727670 yago:Part113809207 yago:PhysicalEntity100001930 yago:PsychologicalFeature100023100 yago:Relation100031921 yago:WikicatKetones dbo:ChemicalCompound yago:Substance100019613 yago:Whole105869584 umbel-rc:ChemicalSubstanceType |
rdfs:comment | Acibenzolar-S-methyl is the ISO common name for an organic compound that is used as a fungicide. Unusually, it is not directly toxic to fungi but works by inducing systemic acquired resistance, the natural defence system of plants. (en) L'acibenzolar-S-méthyl est une substance active de produit phytosanitaire (ou produit phytopharmaceutique, ou pesticide), qui présente un effet fongicide. Analogue de l’acide salicylique, il appartient à la famille chimique des (BTH). Il s"agit du premier produit développé dans les années 1980 et revendiquant un mode d’action de type stimulateur des défenses naturelles des plantes, plus connu sous le nom de BTH et commercialisé par Syngenta aux États-Unis. (fr) Acibenzolar-S-metile è un composto organico fungicida che agisce attivando nelle piante ospitanti i funghi parassiti una difesa autonoma da essi, grazie ad un aumento nella di alcuni geni, come CAD1, NPR1 e PR2. Si tratta di un derivato metilico dell'. (it) Acibenzolar-S-metil (ASM) é um fungicida do grupo químico dos benzothiadiazoles, que tem sido testado como um indutor de resistência em plantas. Não age diretamente sobre o agente patogénico, tendo antes como objetivo ativar naturalmente as defesas da planta, deixando a mesma menos suscetível a doenças e pragas. Deve ser aplicado de forma preventiva, pois ele vai agir sistemicamente, ou seja, vai circular na seiva ativando a resistência da planta de forma generalizada. (pt) Acibenzolar-S-methyl (Abkürzung BTH) ist eine chemische Verbindung, die als Fungizid verwendet wird. BTH leitet sich von Acibenzolar ab. Der Wirkstoff greift in die Salicylsäure-Synthese ein und führt so zur Auslösung einer systemisch aktivierten Resistenz. Es gilt als unbedenklich für den Verbraucher und wird schon bei Tomaten gegen bakterielle Krankheiten eingesetzt. Bei Weintrauben wiesen Versuche nach, dass BTH behandelte Weintrauben mehr Anthocyane (antioxidative Wirkung vermutet) enthielten als unbehandelte. (de) Acibenzolar-S-methyl, een stof die afgeleid is van , is een plantenactivator. Dat wil zeggen dat de stof de natuurlijke weerstand van planten tegen bacteriële en schimmelziekten stimuleert, maar zelf niet actief is tegen die organismen. Het is dus strikt genomen geen fungicide, daar het de schimmels niet vernietigt. De stof wordt ingezet voor de bescherming van planten of zaden van onder meer tarwe, gerst, rijst, tabak, en katoen. De stof heeft daarnaast ook een werking als insecticide. (nl) |
rdfs:label | Acibenzolar-S-methyl (en) Acibenzolar-S-methyl (de) Acibenzolar-S-méthyl (fr) Acibenzolar-S-metile (it) Acibenzolar-S-methyl (nl) Acibenzolar-S-metil (pt) |
owl:sameAs | freebase:Acibenzolar-S-methyl yago-res:Acibenzolar-S-methyl wikidata:Acibenzolar-S-methyl http://azb.dbpedia.org/resource/اسیبنزولار-اس-متیل dbpedia-de:Acibenzolar-S-methyl dbpedia-fa:Acibenzolar-S-methyl dbpedia-fr:Acibenzolar-S-methyl dbpedia-it:Acibenzolar-S-methyl dbpedia-nl:Acibenzolar-S-methyl dbpedia-pt:Acibenzolar-S-methyl dbpedia-sh:Acibenzolar-S-methyl dbpedia-sr:Acibenzolar-S-methyl https://global.dbpedia.org/id/39TFZ |
prov:wasDerivedFrom | wikipedia-en:Acibenzolar-S-methyl?oldid=1110158552&ns=0 |
foaf:depiction | wiki-commons:Special:FilePath/Acibenzolar-S-methyl-3D-spacefill.png wiki-commons:Special:FilePath/Acibenzolar_methyl_ester_synthesis.png wiki-commons:Special:FilePath/S-methyl_benzo(d)(1,2,3)thiadiazole-7-carbothioate_200.svg |
foaf:isPrimaryTopicOf | wikipedia-en:Acibenzolar-S-methyl |
foaf:name | Acibenzolar-S-methyl (en) |
is dbo:wikiPageRedirects of | dbr:C7H4N2OS2 dbr:C8H6N2OS2 dbr:Acibenzolar |
is dbo:wikiPageWikiLink of | dbr:Pathogenesis-related_protein dbr:C7H4N2OS2 dbr:Index_of_pesticide_articles dbr:1,2,3-Benzothiadiazole dbr:C8H6N2OS2 dbr:Economy_of_Florida dbr:Benzothiadiazole dbr:Systemic_acquired_resistance dbr:Acibenzolar |
is foaf:primaryTopic of | wikipedia-en:Acibenzolar-S-methyl |