Publications by authors named "Menegon R"

Article Synopsis
  • * Researchers extracted compounds from A. oleracea using ultrasound-assisted methods and created chitosan membranes, testing their effects on HEp-2 tumor cells through viability assays and a wound healing test.
  • * The results showed that the chitosan membranes with the plant extract significantly reduced tumor cell density and activity, suggesting they could serve as a potential alternative treatment for superficial cancers.
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Numerous natural products have pharmacological activity such that many biologically active compounds have led to the development of cancer chemotherapy drugs. Spilanthes acmella (Asteraceae) is widely cultivated in the State of Pará, Brazil, being employed in folk medicine for its anti-inflammatory, antimicrobial, antioxidant, analgesic, insecticide, and larvicidal properties. However, its cytotoxicity and influence on actin cytoskeleton organisation in tumour cell lines are practically nonexistent.

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The present work reports on the synthesis, biological assaying and docking studies of a series of 12 aryl thiosemicarbazones, which were planned to act over two main enzymes, cruzain and trypanothione reductase. These enzymes are used as targets of trypanocidal activity in Chagas disease control with a minimal mutagenic profile. Three p-nitroaromatic thiosemicarbazones showed high activity against Trypanosoma cruzi in in vitro assays (IC50 < 57 μM), and no mutagenic profile was observed in micronucleous tests.

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Article Synopsis
  • Chlorhexidine (CHX) is a well-known antiplaque agent with side effects that limit its long-term use, leading to poor patient compliance.
  • Researchers hypothesized that a less water-soluble form called chlorhexidine tetrapalmitate (CHXTP) could reduce these side effects while maintaining effectiveness.
  • Tests showed that CHXTP is highly effective against harmful bacteria, doesn't interfere with taste, has low staining potential, but is less retained in saliva compared to traditional CHX formulations.
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The compound 1-(2,6-dichlorophenyl)indolin-2-one (1), planned as a pro-drug of diclofenac (2), was easily synthesized in 94% yield by an intramolecular reaction in the presence of coupling agent (i.e., EDC).

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We report the synthesis and total NMR characterization of 5-thia-1-azabicyclo-[4.2.0]oct-2-ene-2-carboxylic acid-3-[[[(4''-nitrophenoxy)carbonyl]oxy]-methyl]-8-oxo-7-[(2-thienyloxoacetyl)amino]-diphenylmethyl ester-5-dioxide (5), a new cephalosporin derivative.

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Recently, World Health Organization (WHO) and Medicins San Frontieres (MSF) proposed a classification of diseases as global, neglected and extremely neglected. Global diseases, such as cancer, cardiovascular and mental (CNS) diseases represent the targets of the majority of the R&D efforts of pharmaceutical companies. Neglected diseases affect millions of people in the world yet existing drug therapy is limited and often inappropriate.

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