Results 11 to 20 of about 53,724 (334)

Anticancer Activity of Chalcones and Its Derivatives: Review and In Silico Studies

open access: yesMolecules, 2023
Chalcones are direct precursors in the biosynthesis of flavonoids. They have an α,β-unsaturated carbonyl system which gives them broad biological properties.
Fernando Ferreira Leite   +10 more
doaj   +2 more sources

Pharmacological Properties of Chalcones: A Review of Preclinical Including Molecular Mechanisms and Clinical Evidence

open access: yesFrontiers in Pharmacology, 2021
Chalcones are among the leading bioactive flavonoids with a therapeutic potential implicated to an array of bioactivities investigated by a series of preclinical and clinical studies.
Bahare Salehi   +22 more
doaj   +2 more sources

Structural, Vibrational and Electrochemical Analysis and Antibacterial Potential of Isomeric Chalcones Derived from Natural Acetophenone

open access: yesApplied Sciences, 2020
Background: Chalcones are part of a family of small phenolic compounds that are being extensively studied for presenting a diversity of molecular structures and biological activities. In this paper, two chalcones, (E)-1-(2-hydroxy-3,4,6-trimethoxyphenyl)-
Priscila Teixeira da Silva   +15 more
doaj   +2 more sources

Chalcones: Synthetic Chemistry Follows Where Nature Leads

open access: yesBiomolecules, 2021
Chalcones belong to the flavonoid class of phenolic compounds. They form one of the largest groups of bioactive natural products. The potential anticancer, anti-inflammatory, antimicrobial, antioxidant, and antiparasitic properties of naturally occurring
Hiba A. Jasim   +5 more
doaj   +2 more sources

Antitrypanosomal and Antileishmanial Activity of Chalcones and Flavanones from Polygonum salicifolium

open access: yesPathogens, 2021
Trypanosomiasis and leishmaniasis are a group of neglected parasitic diseases caused by several species of parasites belonging to the family Trypansomatida. The present study investigated the antitrypanosomal and antileishmanial activity of chalcones and
Ahmed M. Zheoat   +9 more
doaj   +2 more sources

Chalcones and Dihydrochalcones Augment TRAIL-Mediated Apoptosis in Prostate Cancer Cells [PDF]

open access: yesMolecules, 2010
Chalcones and dihydrochalcones exhibit chemopreventive and antitumor activity. TRAIL (tumor necrosis factor-related apoptosis-inducing ligand) is a natural endogenous anticancer agent.
Almasan   +24 more
core   +4 more sources

Toxicity assessments of chalcone and some synthetic chalcone analogues in a zebrafish model [PDF]

open access: yesMolecules, 2014
[[abstract]]The aim of this study was to investigate the in vivo toxicities of some novel synthetic chalcones. Chalcone and four chalcone analogues 1a–d were evaluated using zebrafish embryos following antibody staining to visualize their morphological ...
Ajaiyeoba   +9 more
core   +6 more sources

Antiproliferative activity and p53 upregulation effects of chalcones on human breast cancer cells

open access: yesJournal of Enzyme Inhibition and Medicinal Chemistry, 2019
Chalcones are valuable structures for drug discovery due to their broad bioactivity spectrum. In this study, we evaluated 20 synthetic chalcones against estrogen-receptor-positive breast cancer cells (MCF-7 line) and triple-negative breast cancer (TNBC ...
Mariana Bastos dos Santos   +10 more
doaj   +2 more sources

Evaluation of the anti-inflammatory effect of chalcone and chalcone analogues in a zebrafish model [PDF]

open access: yesMolecules, 2013
[[abstract]]The aim of this study was to investigate novel chalcones with potent anti-inflammatory activities in vivo. Chalcone and two chalcone analogues (compound 5 and 9) were evaluated using a caudal fin-wounded transgenic zebrafish line “Tg(mpx:gfp)”
Chi-Chung Wen   +5 more
core   +6 more sources

Enantioselective Conjugate Addition of Diethylzinc to Chalcones Catalysed by Chiral Ni(II) Aminoalcohol Complexes [PDF]

open access: green, 1994
Conjugate addition of diethylzinc to chalcones is catalysed by complexes prepared in situ from Ni(acac)2 and cis-exo-N,N-dialkyl-3-aminoisoborneols or (+)-cis-endo-N,N-dimethyl-3-aminoborneol ((+)-DAB) (13b).
Feringa, Bernard   +2 more
core   +4 more sources

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