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Loredana Cappellacci

Researcher at University of Camerino

Publications -  142
Citations -  3475

Loredana Cappellacci is an academic researcher from University of Camerino. The author has contributed to research in topics: Tiazofurin & Adenosine. The author has an hindex of 29, co-authored 131 publications receiving 2753 citations. Previous affiliations of Loredana Cappellacci include University of Rochester Medical Center & Southern Research Institute.

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The essential oil from industrial hemp (Cannabis sativa L.) by-products as an effective tool for insect pest management in organic crops

TL;DR: Light is shed on the possible utilization of the crop residue of industrial hemp as a source of environmental-friendly botanical insecticides to be used in Integrated Pest Management and organic agriculture, particularly to manage aphid and housefly populations.
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Synergized mixtures of Apiaceae essential oils and related plant-borne compounds: Larvicidal effectiveness on the filariasis vector Culex quinquefasciatus Say

TL;DR: The results pointed out the promising potential of four Apiaceae essential oils from Trachyspermum ammi, Smyrnium olusatrum, Pimpinella anisum and Helosciadium nodiflorum to develop cheap and effective mosquito larvicides, as well as the importance to consider the synergistic effects among the tested botanicals during the design of novel mosquito larVicides.
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Mechanisms underlying reductant-induced reactive oxygen species formation by anticancer copper(II) compounds.

TL;DR: Thiol-induced intracellular ROS generation might contribute to the anticancer activity of copper thiosemicarbazone complexes but is not the determining factor, while experiments on generation of oxidative stress and the influence of biologically relevant reductants revealed that reductant-dependent redox cycling occurred mainly outside the cells.
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Furanfurin and thiophenfurin: two novel tiazofurin analogues. Synthesis, structure, antitumor activity, and interactions with inosine monophosphate dehydrogenase.

TL;DR: The results obtained support the hypothesis that the presence of S in the heterocycle in position 2 with respect to the glycosidic bond is essential for the cytotoxicity and IMP dehydrogenase activity of tiazofurin, while the N atom is not.