Synthesis and evaluation of modified chalcone based p53 stabilizing agents

S Iftikhar, S Khan, A Bilal, S Manzoor… - Bioorganic & medicinal …, 2017 - Elsevier
Tumor suppressor protein p53 induces cell cycle arrest and apoptotic cell death in response
to various cellular stresses thereby preventing cancer development. Activation and …

Licochalcone B induces apoptosis of human oral squamous cell carcinoma through the extrinsic-and intrinsic-signaling pathways

H Oh, G Yoon, JC Shin, SM Park… - International …, 2016 - spandidos-publications.com
Abstract Licochalcone B (Lico B), which belongs to the retrochalcone family, is isolated from
the roots of Chinese licorice. Lico B has been reported to have several other useful …

Structure–Activity Relationship Studies of Chalcones and Diarylpentanoids with Antitumor Activity: Potency and Selectivity Optimization

J Moreira, JB Loureiro, D Correia, A Palmeira… - Pharmaceuticals, 2023 - mdpi.com
We previously reported that chalcone CM-M345 (1) and diarylpentanoid BP-C4 (2) induced
p53-dependent growth inhibitory activity in human cancer cells. Herein, CM-M345 (1) and …

Novel halogenated pyrazine-based chalcones as potential antimicrobial drugs

M Kucerova-Chlupacova, V Vyskovska-Tyllova… - Molecules, 2016 - mdpi.com
Chalcones, ie, compounds with the chemical pattern of 1, 3-diphenylprop-2-en-1-ones, exert
a wide range of bio-activities, eg, antioxidant, anti-inflammatory, anticancer, anti-infective …

Synthesis of chalcone derivatives by Claisen-Schmidt condensation and in vitro analyses of their antiprotozoal activities

GB Souza, TAC Santos, APS Silva… - Natural Product …, 2024 - Taylor & Francis
Chalcone is a molecule with known biological activities. Based on this, a series of chalcone
derivatives bearing methyl, phenyl or furanyl substituents at different positions of A and B …

Computer-aided drug design applied to secondary metabolites as anticancer agents

RSA de Araújo, EF da Silva-Junior… - Current Topics in …, 2020 - ingentaconnect.com
Computer-Aided Drug Design (CADD) techniques have garnered a great deal of attention in
academia and industry because of their great versatility, low costs, possibilities of cost …

Spotlight on 4‐substituted quinolines as potential anti‐infective agents: Journey beyond chloroquine

A Goyal, H Kharkwal, M Piplani, Y Singh… - Archiv der …, 2023 - Wiley Online Library
Continued emerging resistance of pathogens against the clinically approved candidates and
their associated limitations continuously demand newer agents having better potency with a …

[HTML][HTML] Improved eradication efficacy of a combination of newly identified antimicrobial agents in C. albicans and S. aureus mixed-species biofilm

F Bonvicini, F Belluti, A Bisi, S Gobbi, I Manet… - Research in …, 2021 - Elsevier
Candida albicans and Staphylococcus aureus are common human pathogens, frequently
isolated independently or co-isolated from bloodstream infections, and able to form dense …

Synthesis, structure and in vitro anti-trypanosomal activity of non-toxic arylpyrrole-based chalcone derivatives

AI Zulu, OO Oderinlo, C Kruger, M Isaacs, HC Hoppe… - Molecules, 2020 - mdpi.com
With an intention of identifying chalcone derivatives exhibiting anti-protozoal activity, a
cohort of relatively unexplored arylpyrrole-based chalcone derivatives were synthesized in …

Cis and trans isomers of 1-(5-bromothiophen-2-yl)-3-(10-chloroanthracen-9-yl) prop-2-en-1-one: Synthesis and characterization

P Naresh, B Pramodh, S Naveen, S Ganguly… - Journal of Molecular …, 2021 - Elsevier
Chalcone derivatives are simple chemical scaffold found in natural products and have been
extensively used as an effective template in medicinal chemistry for drug discovery. Two …