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 - benthamdirect.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 …

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

N Padauleng, M Mustofa… - … Pacific Journal of …, 2023 - pmc.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 …

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 …

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 …

Molecular Docking and Molecular Dynamic Investigations of Xanthone-Chalcone Derivatives against Epidermal Growth Factor Receptor for Preliminary Discovery of …

YS Kurniawan, E Yudha, G Nugraha… - Indonesian Journal of …, 2024 - journal.ugm.ac.id
Epidermal growth factor receptor (EGFR) is found to be overexpressed in cancer cells as it
controls angiogenesis, cell signaling, and proliferation mechanisms. Therefore, EGFR has …

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

FE Mulyana, SSW Waskitha, D Pranowo… - …, 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 …

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 …

Synthesis, antimalarial activity assay and molecular docking study of N-substituted chloro-pyrazolines

M Wiratama, SSW Waskitha, W Haryadi… - Tropical Journal of …, 2022 - ajol.info
Purpose: To synthesize chloro-pyrazolines (A–D), determine their antimalarial activity
against Plasmodium falciparum strain 3D7 in vitro, and understand the interaction between …