Results 151 to 160 of about 736,450 (179)
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Chemical sensing of chalcones by voltammetry: trans-Chalcone, cardamonin and xanthohumol
Electrochimica Acta, 2013Abstract Xanthohumol (XN) and cardamonin (CD) belong to the chemical class of chalcones which are phenolic compounds of large interest due to their health promoting properties. In the present work, their electrochemical behavior on a hanging mercury drop electrode (HMDE) is compared to trans -chalcone by means of cyclic voltammetry (CV).
Tavares, E.M. +8 more
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Electronic absorption spectra of heterocyclic analogs of trans-chalcone
Chemistry of Heterocyclic Compounds, 1977Thiophene, furan, and pyrrole analogs of trans-chalcone have UV spectra consisting of bands belonging to the spectra of the corresponding 2-acetylhetaryls and 2-hetarylideneacetones that are shifted bathochromically as a result of mutual perturbation of these two crossconjugated fragments.
M. Reinkhardt +3 more
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Abstract 4654: Antitumorigenic activity of trans-chalcone in osteosarcoma
Cancer Research, 2015Abstract Background and Aims: Osteosarcoma is the most common bone cancer, and it affects mostly teenagers and children. Although the emergence of multidrug therapies has improved available treatments for osteosarcoma, approximately 30% of patients will still develop metastasis.
Gabriel da Silva +3 more
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International Journal of Pharmaceutics, 2023
Improved therapies for inflammatory bowel diseases are sorely needed. Novel therapeutic agents and the development of controlled release systems for targeted tissue delivery are interesting approaches to overcome these barriers. We investigated the activity of trans-chalcone (T) in acetic acid-induced colitis in mice and developed, characterized, and ...
Carla F.S. Guazelli +10 more
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Improved therapies for inflammatory bowel diseases are sorely needed. Novel therapeutic agents and the development of controlled release systems for targeted tissue delivery are interesting approaches to overcome these barriers. We investigated the activity of trans-chalcone (T) in acetic acid-induced colitis in mice and developed, characterized, and ...
Carla F.S. Guazelli +10 more
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Journal of Polymer Engineering, 2022
Abstract In this study, controlled release of trans-chalcone was achieved by using a polycaprolactone-based hybrid system as the drug carrier material. Encapsulation efficiency was obtained in the range of 70–75% for various formulations and in vitro release studies, conducted at 37 °C and pH 7.4, revealed slow profile reaching 60 ...
Yasemin Kaptan, Yüksel Güvenilir
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Abstract In this study, controlled release of trans-chalcone was achieved by using a polycaprolactone-based hybrid system as the drug carrier material. Encapsulation efficiency was obtained in the range of 70–75% for various formulations and in vitro release studies, conducted at 37 °C and pH 7.4, revealed slow profile reaching 60 ...
Yasemin Kaptan, Yüksel Güvenilir
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Solubility enhancement of trans-chalcone using lipid carriers and supercritical CO2 processing
The Journal of Supercritical Fluids, 2009Abstract This work studies the possibility of enhancing the solubility of 1,3-diphenyl-2-propenone, the core structure of chalcones, through lipidic formulations under supercritical CO 2 processing. Microparticles of chalcone, alone and with lipid carriers, were produced by PGSS ® , a method which involves the quick depressurization of a gas ...
A.R. Sampaio de Sousa +5 more
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European Journal of Pharmacology, 2019
Leishmania parasites infect macrophages causing a wide spectrum of human diseases encompassing from cutaneous to visceral forms. The drugs currently used in leishmaniasis treatment are highly toxic and associated with acquired resistance. Seeking novel therapeutic targets, we conducted a comprehensive in vitro study to investigate the action of trans ...
Milena Menegazzo, Miranda-Sapla +14 more
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Leishmania parasites infect macrophages causing a wide spectrum of human diseases encompassing from cutaneous to visceral forms. The drugs currently used in leishmaniasis treatment are highly toxic and associated with acquired resistance. Seeking novel therapeutic targets, we conducted a comprehensive in vitro study to investigate the action of trans ...
Milena Menegazzo, Miranda-Sapla +14 more
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Organic & Biomolecular Chemistry, 2017
Rigidifying 4′,7-dihydroxyflavylium prevents the formation of trans-chalcone (Ct). The addition of CTAB micelles unveils Ct enabling photochromism. Disrupting the micelles with α-cyclodextrin returns the system to its initial state.
Márcia, Pessêgo +6 more
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Rigidifying 4′,7-dihydroxyflavylium prevents the formation of trans-chalcone (Ct). The addition of CTAB micelles unveils Ct enabling photochromism. Disrupting the micelles with α-cyclodextrin returns the system to its initial state.
Márcia, Pessêgo +6 more
openaire +2 more sources
Anti-cancer activity of trans-chalcone in osteosarcoma: Involvement of Sp1 and p53.
Molecular carcinogenesis, 2017Osteosarcoma is the most common bone cancer. Although the emergence of multidrug therapies has improved available treatments for osteosarcoma, approximately 30% of patients will still develop metastasis. Currently, much anticancer therapy uses drugs that affect oncogenes/tumor suppressor genes, such as p53 (up-regulation) and Sp1 (down-regulation ...
Gabriel, Silva +4 more
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Kinetics and mechanism of reactions of cis- and trans-chalcones with amines
Journal of the American Chemical Society, 1969F M, Menger, J H, Smith
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