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Renner G, Ruckdeschel G. Effects of pentachloronitrobenzene and some of its known and possible metabolites on fungi. Appl Environ Microbiol. 1983;46(3):765-8doi: 10.1128/aem.46.3.765-768.1983.
Renner, G., & Ruckdeschel, G. (1983). Effects of pentachloronitrobenzene and some of its known and possible metabolites on fungi. Applied and environmental microbiology, 46(3), 765-8. https://doi.org/10.1128/aem.46.3.765-768.1983
Renner, G, and Ruckdeschel, G. "Effects of pentachloronitrobenzene and some of its known and possible metabolites on fungi." Applied and environmental microbiology vol. 46,3 (1983): 765-8. doi: https://doi.org/10.1128/aem.46.3.765-768.1983
Renner G, Ruckdeschel G. Effects of pentachloronitrobenzene and some of its known and possible metabolites on fungi. Appl Environ Microbiol. 1983 Sep;46(3):765-8. doi: 10.1128/aem.46.3.765-768.1983. PMID: 16346392; PMCID: PMC239349.
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Appl Environ Microbiol. 1983 Sep;46(3):765-8. doi: 10.1128/aem.46.3.765-768.1983.

Effects of pentachloronitrobenzene and some of its known and possible metabolites on fungi.

Applied and environmental microbiology

G Renner, G Ruckdeschel

Affiliations

  1. Institut für Pharmakologie und Toxikologie and Max von Pettenkofer-Institut für Hygiene und Medizinische Mikrobiologie der Universität München, D-8000 Munich 2, Federal Republic of Germany.

PMID: 16346392 PMCID: PMC239349 DOI: 10.1128/aem.46.3.765-768.1983

Abstract

Fungicidal activities of pentachloronitrobenzene and derivatives were tested with Candida albicans, Aspergillus fumigatus, Trichophyton rubrum, Trichophyton mentagrophytes, and Microsporon canis. In relation to pentachloronitrobenzene, no increasing fungistatic activities were found with cysteine derivatives. Rising fungistatic activities were seen with pentachlorophenylmethylsulfone and, in some of the strains, with pentachloronitrosobenzene, pentachlorothiophenol, pentachlorophenol, pentachloroaniline, pentachlorophenylmethylsulfoxide, the isomeric tetrachloronitrobenzenes, tetrachlorothiophenols, tetrachlorophenols, and tetrachloroanilines.

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