1971
DOI: 10.1007/978-3-662-11311-0
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Chemistry of Fungicidal Action

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Cited by 54 publications
(37 citation statements)
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“…This result confirms captan non-specific thiol reactivity as one of the most important direct effects of the phtalimide fungicides [3]. Moreover, captan-treated cells exhibited a drastic loss of membrane integrity, a typical necrotic behavior [16], which can be the result of the modification of membrane protein structures by protein sulfhydryldisulfide transitions, and consequent increase in membrane permeability [17].…”
Section: Resultssupporting
confidence: 68%
See 1 more Smart Citation
“…This result confirms captan non-specific thiol reactivity as one of the most important direct effects of the phtalimide fungicides [3]. Moreover, captan-treated cells exhibited a drastic loss of membrane integrity, a typical necrotic behavior [16], which can be the result of the modification of membrane protein structures by protein sulfhydryldisulfide transitions, and consequent increase in membrane permeability [17].…”
Section: Resultssupporting
confidence: 68%
“…Captan reaction with thiol groups has been pointed as the main mode of action on phytopathogenic fungi, been responsible for the reduction of enzymatic activities, respiration, physiological changes, and fungal death [3]. In the presence of exposed thiol groups, captan oxidize thiols and is hydrolyze to its reactive thiophosgene (SCCl 3 ) moiety, and the 1,2,3,6-tetrahydrophthalimide ring [4].…”
Section: Introductionmentioning
confidence: 99%
“…tricarboxylic acid enzymes, hexokinase enzymes, triosphosphate dehydrogenase enzymes, aldolase enzymes, cocarboxylase enzymes, thiamin pyrophosphate enzymes, keto acid dehydrogenase enzymes, polyphenol oxidase enzymes, citric acid synthetase enzymes, akonitase enzymes, isositrate dehydrogenase enzymes, α-ketoglutarate dehydrogenase enzymes, succinate dehydrogenase enzymes, malate dehydrogenase enzymes and glycolytic enzymes (hexokinase, phosphohexose isomerase, phosphofructokinase, aldolase, triosa phosphate isomerase, glyceraldehyde 3-phosphate dehydrogenase, phosphoglycerate kinase, phosphoglycerate mutase, enolase and pyruvate kinase) [17].…”
Section: Discussionmentioning
confidence: 99%
“…Affects the respiratory complexes of mitochondria by disrupting the flow of electrons in the respiratory chain, causing multi-site toxicity on a broad spectrum [15,16]. Affects enzymes in mitochondria [17]. Calcium polysulfide toxicity against non-target organisms is between non-toxic to moderate toxicity [18][19][20][21].…”
mentioning
confidence: 99%
“…The inhibitory power of substituted quinones largely depends upon their substituent group. It was found that halogenation increased inhibitory effectiveness hence chloranil (tetrachloro-1,4-benzoquinone) and dichlone (2,3-dichloro-1,4-naphthoquinone) are fungicides most frequently used [19].…”
Section: Introductionmentioning
confidence: 99%