Synthesis and pharmacological properties of chalcones: a review

Design of potent fluoro-substituted chalcones as antimicrobial agents

(2017) Serdar Burmaoglu et al.   JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY

Synthesis and Biological Evaluation of Novel Bischalcone Derivatives as Carbonic Anhydrase Inhibitors

(2016) Tayfun Arslan et al.   ARCHIV DER PHARMAZIE

Synthesis and carbonic anhydrase inhibitory properties of novel chalcone substituted benzenesulfonamides

(2016) Tayfun Arslan et al.   BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

A convenient synthesis of coumarinyl chalcones using HClO4–SiO2: A green approach

(2015) Zeba N. Siddiqui   Arabian Journal of Chemistry

One-Pot Synthesis of Aminoindolizines and Chalcones Using CuI/CSP Nanocomposites with Anomalous Selectivity under Green Conditions

(2015) U. Chinna Rajesh et al.   ACS Sustainable Chemistry & Engineering

Antiobesity, antioxidant and cytotoxicity activities of newly synthesized chalcone derivatives and their metal complexes

(2014) Mohamed Ramadan El Sayed Aly et al.   EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

Design, economical synthesis and antiplasmodial evaluation of vanillin derived allylated chalcones and their marked synergism with artemisinin against chloroquine resistant strains of Plasmodium falciparum

(2014) Nandini Sharma et al.   EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

Antimalarial Activity of Newly Synthesized Chalcone Derivatives In Vitro

(2012) Neesha Yadav et al.   Chemical Biology & Drug Design

Trimethoxy-chalcone derivatives inhibit growth of Leishmania braziliensis: Synthesis, biological evaluation, molecular modeling and structure–activity relationship (SAR)

(2011) Murilo Lamim Bello et al.   BIOORGANIC & MEDICINAL CHEMISTRY

Enone– and Chalcone–Chloroquinoline Hybrid Analogues: In Silico Guided Design, Synthesis, Antiplasmodial Activity, in Vitro Metabolism, and Mechanistic Studies

(2011) Eric M. Guantai et al.   JOURNAL OF MEDICINAL CHEMISTRY

Synthesis of chalcones catalyzed by aminopropylated silica sol–gel under solvent-free conditions

(2011) Gustavo Romanelli et al.   JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL

Synthesis of novel α-pyranochalcones and pyrazoline derivatives as Plasmodium falciparum growth inhibitors

(2010) Gajanan Wanare et al.   BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

Fluorinated 2′-hydroxychalcones as garcinol analogs with enhanced antioxidant and anticancer activities

(2010) Subhash Padhye et al.   BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

Synthesis and biological evaluation of indolyl chalcones as antitumor agents

(2010) Dalip Kumar et al.   BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

Chromene-Based Synthetic Chalcones as Potent Antileishmanial Agents: Synthesis and Biological Activity

(2010) Alireza Foroumadi et al.   Chemical Biology & Drug Design

Synthesis and biological evaluation of β-chloro vinyl chalcones as inhibitors of TNF-α and IL-6 with antimicrobial activity

(2010) Babasaheb P. Bandgar et al.   EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

Hydroxychalcones as potent antioxidants: Structure–activity relationship analysis and mechanism considerations

(2010) Yi-Ping Qian et al.   FOOD CHEMISTRY

Synthesis, antioxidant evaluation, and quantitative structure–activity relationship studies of chalcones

(2010) P. M. Sivakumar et al.   MEDICINAL CHEMISTRY RESEARCH

Novel antileishmanial chalconoids: Synthesis and biological activity of 1- or 3-(6-chloro-2H-chromen-3-yl)propen-1-ones

(2009) Zohreh Nazarian et al.   EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

Synthesis of new chalcone derivatives containing acridinyl moiety with potential antimalarial activity

(2009) V. Tomar et al.   EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

Palladium-Catalyzed Cyclocarbonylation-Decarboxylation of Diethyl(2-iodoaryl)malonates with Vinyl Ketones Affording Functionalized Enolic 2-Acyl-3,4-dihydronaphthalenones

(2009) Zhaoyan Zheng et al.   ORGANIC LETTERS

Synthesis, physicochemical properties and antimicrobial evaluation of new (E)-chalcones

(2007) Z. Nowakowska et al.   EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY