Stereoselective synthesis of flavonoids: A brief overview

AM Pereira, H Cidade, ME Tiritan - Molecules, 2023 - mdpi.com
Stereoselective synthesis has been emerging as a resourceful tool because it enables the
obtaining of compounds with biological interest and high enantiomeric purity. Flavonoids are …

Recent advances in chalcone-based anticancer heterocycles: A structural and molecular target perspective

V Kumar, S Dhawan, PS Girase… - Current Medicinal …, 2021 - ingentaconnect.com
Chalcones are an interesting class of compounds endowed with a plethora of biological
activities beneficial to human health. These chemotypes have continued to attract increased …

Design, synthesis and neuropharmacological evaluation of new 2, 4-disubstituted-1, 5-benzodiazepines as CNS active agents

R Verma, R Bhatia, G Singh, B Kumar, S Mehan… - Bioorganic …, 2020 - Elsevier
Benzodiazepines (BZDs) represent a class of privilege scaffold in the modern era of
medicinal chemistry as CNS active agents and BZD based drugs are used to treat different …

Experimental and Theoretical Studies of the Pyrazoline Derivative 5-(4-methylphenyl)-3-(5-methylfuran-2-yl)-1-phenyl-4,5-dihydro-1H-Pyrazole and its Application for Selective …

P Sharma, S Bhogal, A Lealam, S Kumar, M Yusuf… - Journal of …, 2022 - Springer
Abstract A simple fluorescent chemosensor 5-(4-methylphenyl)-3-(5-methylfuran-2-yl)-1-
phenyl-4, 5-dihydro-1 H-pyrazole (PY) has been synthesized for the detection of Cd2+ ion …

[HTML][HTML] Chalcone-3 inhibits the proliferation of human breast cancer MDA-MB-231 cell line

N Padauleng, M Mustofa… - Asian Pacific Journal …, 2023 - ncbi.nlm.nih.gov
Objective: Chalcone-3 has been shown to be cytotoxic and selective against luminal
subtype breast cancer cell lines, which are suspected to occur through the mechanism of …

[PDF][PDF] Synthesis of chalcone derivatives with methoxybenzene and pyridine moieties as potential antimalarial agents.

FE Mulyana, SS Wira Waskitha… - Pharmacia (0428 …, 2023 - pharmacia.pensoft.net
Malaria remains an endemic disease in tropical regions, urgently needed the search for
effective antimalarial agents due to resistance against existing drugs. This study investigated …

Synthesis, cytotoxicity evaluation and molecular docking study of N-phenylpyrazoline derivatives

AAT Suma, TD Wahyuningsih… - Indonesian Journal of …, 2019 - journal.ugm.ac.id
The synthesis of N-phenylpyrazolines 1-5 was performed by the cyclocondensation of
phenylhydrazine and appropriate chalcones that have been synthesized from our previous …

Synthesis of some chalcone derivatives, in vitro and in silico toxicity evaluation

AN Kristanti, H Suwito, NS Aminah… - Rasayan Journal of …, 2020 - repository.unair.ac.id
Chalcone can be synthesized using some methods, but conventional Claisen-Schmidt
condensation is still the best method. The objevtives of this study were to synthesize some …

QSAR approach and synthesis of chalcone derivatives as antimalarial compound against Plasmodium falciparum 3D7 Strain.

SSW Waskitha, FE Mulyana, NF Riza… - Rasayan Journal of …, 2021 - search.ebscohost.com
A quantitative structure-activity relationship (QSAR) analysis of serial chalcone derivatives
as antimalarial agents against Plasmodium falciparum strain 3D7 (Pf3D7) was conducted, it …

[PDF][PDF] Molecular interaction of the downstream executioner cysteine aspartyl proteases (caspase-3 and caspase-7) with corilagin, quercetin, rutin, kaempferol, gallic …

S Megantara, M Mutakin, E Halimah… - Rasayan J Chem …, 2020 - rasayanjournal.co.in
Apoptosis is caused by activation of caspases, ie intracellular cysteine proteases which
cleave their substrates at aspartic acid residues. Caspases are categorized into (1) the …