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Dithiocarbamate

About: Dithiocarbamate is a research topic. Over the lifetime, 2996 publications have been published within this topic receiving 41318 citations. The topic is also known as: dithiocarbamates.


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Journal ArticleDOI
TL;DR: A series of N-mono- and N,N-disubstituted dithiocarbamates investigated as inhibitors of two β-carbonic anhydrases may have the potential for developing antimycobacterial agents with a diverse mechanism of action compared to the clinically used drugs.
Abstract: A series of N-mono- and N,N-disubstituted dithiocarbamates have been investigated as inhibitors of two β-carbonic anhydrases (CAs, EC 4211) from the bacterial pathogen Mycobacterium tuberculosis, mtCA 1 (Rv1284) and mtCA 3 (Rv3273) Both enzymes were inhibited with efficacies between the subnanomolar to the micromolar one, depending on the substitution pattern at the nitrogen atom from the dithiocarbamate zinc-binding group Aryl, arylalkyl-, heterocyclic as well as aliphatic and amino acyl such moieties led to potent mtCA 1 and 3 inhibitors in both the N-mono- and N,N-disubstituted dithiocarbamate series This new class of β-CA inhibitors may have the potential for developing antimycobacterial agents with a diverse mechanism of action compared to the clinically used drugs for which many strains exhibit multi-drug/extensive multi-drug resistance

130 citations

Journal ArticleDOI
Xiaosheng Jing1, Fuqiang Liu1, Xin Yang1, Panpan Ling1, Lanjuan Li1, Chao Long1, Aimin Li1 
TL;DR: The strong affinity of PSDC toward these target soft acids could be well demonstrated with the electrostatic attraction and chelating interaction caused by IDA moiety and sulphur which were namely soft bases on the concept of hard and soft acids and bases (HASB).

129 citations

Journal ArticleDOI
TL;DR: Analysis of apple, tomato, and papaya samples with field-incurred dithiocarbamate residues showed comparable results using both the traditional and the new reaction systems, which are less fragile than the traditional design, easier to assemble, and allows for a higher sample throughput.
Abstract: Dithiocarbamates are a class of fungicides extensively used in many crops worldwide. The current residue definition of dithiocarbamates in food for compliance with maximum residue limits, at national and international levels, is total residues arising from the use of any or each dithiocarbamate fungicide, determined as CS2. The analytical method most frequently used to analyze dithiocarbamate residues in food for monitoring purposes was proposed more than 30 years ago. In this method, total dithiocarbamates are decomposed to CS2, which is purified and reacted with a cupric reagent. The yellow complex formed is quantified by spectrophotometry. In this paper, a new reaction system for the purification and complexation of CS2 is proposed. The new system is less fragile than the traditional design, is easier to assemble, and allows for a higher sample throughput, in addition to being of low cost. Recovery of added mancozeb, thiram, or ziram (0.15−8.0 mg/kg) in rice, beans, apple, banana, orange, papaya, tomat...

128 citations

Journal ArticleDOI
TL;DR: The thiuram disulfide disulfiram (DSF) was found to induce glutathione oxidation, DNA fragmentation, and cell killing more potently than its parent dithiocarbamate, DDC, of particular importance was the finding that the actions of DSF were less prone to inhibition by the removal of external copper ions with a chelating agent.

127 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
202377
2022156
202173
202088
2019100
201891