2H/4H-Chromenes—A versatile biologically attractive Scaffold
2H/4H-chromene (2H/4H-ch) is an important class of heterocyclic compounds with versatile
biological profiles, a simple structure, and mild adverse effects. Researchers discovered …
biological profiles, a simple structure, and mild adverse effects. Researchers discovered …
Recent developments in biological aspects of chalcones: the odyssey continues
Introduction: Chalcones are attractive to synthetic chemists because they are easy to
prepare, have a large number of replaceable hydrogens, thereby having significant …
prepare, have a large number of replaceable hydrogens, thereby having significant …
Flavones and related compounds: synthesis and biological activity
This review focuses on the synthesis and biological activity of flavones and their related
flavonoidic compounds, namely flavonols and aurones. Among the biological activities of …
flavonoidic compounds, namely flavonols and aurones. Among the biological activities of …
Synthesis and biological evaluation of halogenated phenoxychalcones and their corresponding pyrazolines as cytotoxic agents in human breast cancer
Novel halogenated phenoxychalcones 2a–f and their corresponding N-acetylpyrazolines 3a–
f were synthesised and evaluated for their anticancer activities against breast cancer cell …
f were synthesised and evaluated for their anticancer activities against breast cancer cell …
Chalcone scaffolds as anticancer drugs: a review on molecular insight in action of mechanisms and anticancer properties
Cancer is the deadliest disease worldwide and the development of safer chemical entities to
treat cancer is one of the major challenges of medicinal chemistry. The emergence of new …
treat cancer is one of the major challenges of medicinal chemistry. The emergence of new …
In vivo and in vitro anti-inflammatory, antipyretic and ulcerogenic activities of pyridone and chromenopyridone derivatives, physicochemical and pharmacokinetic …
EA Fayed, AH Bayoumi, AS Saleh, EME Al-Arab… - Bioorganic …, 2021 - Elsevier
Throughout this study, we present the victorious synthesis of a novel class of 2 (1H)-
pyridone molecules, bearing a 4-hydroxyphenyl moiety through a one-pot reaction of 2 …
pyridone molecules, bearing a 4-hydroxyphenyl moiety through a one-pot reaction of 2 …
Design, synthesis, and biological evaluation of novel pyrrolo [1, 2-a] pyrazine derivatives
J Kim, M Park, J Choi, DK Singh, HJ Kwon… - Bioorganic & Medicinal …, 2019 - Elsevier
Abstract A pyrrolo [1, 2-a] pyrazine-based chemical territory was expanded via construction
of new chemical library with distinctive substitution patterns, which was made possible by …
of new chemical library with distinctive substitution patterns, which was made possible by …
Design, synthesis, and carbonic anhydrase inhibition activity of benzenesulfonamide-linked novel pyrazoline derivatives
Abstract Carbonic anhydrases (CA, EC 4.2. 1.1) are Zinc metalloenzymes and are present
throughout most living organisms. Among the catalytically active isoforms are the cytosolic …
throughout most living organisms. Among the catalytically active isoforms are the cytosolic …
Unravelling the anticancer potential of functionalized chromeno [2, 3-b] pyridines for breast cancer treatment
S Oliveira-Pinto, O Pontes, D Lopes… - Bioorganic …, 2020 - Elsevier
A selection of new chromeno [2, 3-b] pyridines was prepared from chromenylacrylonitriles
and N-substituted piperazines, using a novel and efficient synthetic procedure. The …
and N-substituted piperazines, using a novel and efficient synthetic procedure. The …
Ru (II)-Catalyzed Asymmetric Transfer Hydrogenation of Chalcones in Water: Application to the Enantioselective Synthesis of Flavans BW683C and Tephrowatsin E
FC Demidoff, GS Caleffi, M Figueiredo… - The Journal of Organic …, 2022 - ACS Publications
The oxo-tethered-Ru (II) precatalyst promoted the one-pot C═ C/C═ O reduction of
chalcones using sodium formate as the hydrogen source in water through asymmetric …
chalcones using sodium formate as the hydrogen source in water through asymmetric …