Multiple sensitization due to bis‐dithiocarbamate and thiophthalimide pesticides

Peluso, Anna Maria; Tardio, M; Adamo, F; Venturo, Nicola

doi:10.1111/j.1600-0536.1991.tb01885.x

Cited by 21 publications

(6 citation statements)

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“…Typical cases described from The Netherlands included two office workers who had purchased maneb spray to care for the plants in their office and a 51-year-old woman who worked as an assistant in a flower shop (Nater et al, 1979). Similar cases have been reported from the United States (Adams and Manchester, 1982), Italy (Peluso et al, 1991), and Germany (Koch, 1996). A case reported from Japan identified mancozeb as a cause of allergic contact dermatitis and photodermatitis (Higo et al, 1996).…”

Section: Sensitization Studiesmentioning

confidence: 75%

The Regulatory Evaluation of the Skin Effects of Pesticides

O’Malley

2010

Hayes' Handbook of Pesticide Toxicology

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Section: Sensitization Studiesmentioning

confidence: 75%

The Regulatory Evaluation of the Skin Effects of Pesticides

O’Malley

2010

Hayes' Handbook of Pesticide Toxicology

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“…In this communication, we report the isolation from the leaves of P. pedicellatum and characterization of a new compound, designated as pedicellamide (1), and its antifungal and antioxidant properties. The structure of the compound has been established through 1 H and 13 C NMR spectroscopy and confirmed by single crystal X-ray crystallography. The antifungal properties of the isolated compound were measured against the plant pathogenic fungi R. solani, F. oxysporum, A. niger, P. gramini and C. lunata.…”

mentioning

confidence: 99%

“…Rhizoctonia solani, Fusarium oxysporum, Aspergillus niger, Puccinia gramini and Curvularia lunata are major causes of fungal infection in several important crops [2][3][4][5][6][7][8][9]. Existing antifungal agents are mostly of synthetic origin and are reported to have a number of side effects, such as acute renal failure, hepatotoxicity, toxic porphyria, hemolytic anemia, neuropathy, asthma, dermatitis, and hemolysis [10][11][12][13][14][15][16][17][18][19]. Moreover, the emerging resistance of many of these fungi to different fungicides is also an alarming concern [20][21][22][23].…”

mentioning

confidence: 99%

“…Two doublets at δ 6.45 and δ 6.29, with J = 2 Hz, and each integrating for two protons, were assigned to the presence of two protons at C-α and C-β, respectively, in a pyrrole ring system. In the 13 C NMR spectrum the peak at δ 169.45 revealed the presence of a carbonyl carbon. Other 13 C signals were at δ 30.4, 36.6, 55.9, 104.6, 112.9, 118.6, 131, 132.8, and 146 ppm.…”

mentioning

confidence: 99%

“…In the 13 C NMR spectrum the peak at δ 169.45 revealed the presence of a carbonyl carbon. Other 13 C signals were at δ 30.4, 36.6, 55.9, 104.6, 112.9, 118.6, 131, 132.8, and 146 ppm. NMR data are presented in Table 1.…”

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confidence: 99%

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Antifungal and Antioxidant Pyrrole Derivative from Piper Pedicellatum

Tamuly

Dutta

Bordoloi

et al. 2013

Natural Product Communications

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In continuation of our search for efficient pest control natural products from the flora of the South Eastern Sub-Himalayan biodiversity region, we have investigated wild edible Piper pedicellatum C. DC (Piperaceae) from Arunachal Pradesh, India against five important plant pathogenic fungi through an activity guided method, and a new compound, pedicellamide, was isolated. The structure was determined on the basis of extensive spectroscopic studies and confirmed by X-ray crystallography. The compound exhibited antifungal activities against the phytopathogenic fungal organisms Rhizoctonia solani (MIC 38.4 ± 1.6 μg/mL), Fusarium oxysporum (MIC 29.7 ± 0.8 μg/mL), Aspergillus niger (MIC 48.6 ± 0.7 μg/mL), Puccinia gramini (MIC 46.8 ± 1.4 μg/mL) and Curvularia lunata (MIC 49.1 ± 0.1μg/mL). Additionally, the antioxidant potential of the compound was estimated by DPPH, ABTS and FRAP assay and found to be 2.87 ± 0.20, 2.19 ± 0.13 and 3.96 ± 0.17 VCEAC (μM/g), respectively.

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Selected Aliphatic and Aromatic Nitrogen Compounds

Ziegler‐Skylakakis

2023

Patty's Toxicology

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This is an update of a previous chapter. It presents an evaluation of the toxicological potential of a number of aliphatic and aromatic nitrogen compounds, with information on their use, production, and exposure scenarios. These compounds were originally selected on the basis of their use in industry. In general, there has been little new information published in the literature that has significantly altered the previous profile of each compound. The three‐membered ring compounds discussed are ethyleneimine, propylenenimine, and triethylenemelamine. They are alkylating agents and have toxicological properties similar to nitrogen mustards. Six nitrogen mustards and their hydrochlorides are discussed as a group of chemicals. Furthermore, data on representatives of five‐membered ring nitrogen compounds (pyrrolidine, N ‐methyl‐2‐pyrrolidone) and of six‐membered ring compounds (piperidine, piperazine, morpholine, and hexamethylenetetramine) are included. Captan, captafol, and folpet—three N ‐sulfenyl phthalimide fungicides—and benomyl, carbendazim, and thiophanate‐methyl—benzimidazole fungicides—are evaluated as separate groups. Data on 1‐ H ‐benzotriazol are also included in this chapter. The subchapter of each compound or group of compounds includes the physical and chemical properties, information as to use and production, data on the toxicological potential, and standards, regulations, or guidelines of exposure. In addition, data on the environmental impact of each compound or group of compounds are presented and evaluated.

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Multiple sensitization due to bis‐dithiocarbamate and thiophthalimide pesticides

Cited by 21 publications

References 1 publication

The Regulatory Evaluation of the Skin Effects of Pesticides

The Regulatory Evaluation of the Skin Effects of Pesticides

Antifungal and Antioxidant Pyrrole Derivative from Piper Pedicellatum

Selected Aliphatic and Aromatic Nitrogen Compounds

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