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Published in 2020 at "ChemMedChem"
DOI: 10.1002/cmdc.202000002
Abstract: A series of novel quinoline and quinolinium iodide derivatives were designed and synthesized to discover potential anticancer and antibacterial agents. With regard to anticancer properties, in vitro cytotoxicities against three human cancer cell lines (A‐549, HeLa…
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Keywords:
quinolinium iodide;
quinoline quinolinium;
antibacterial agents;
anticancer antibacterial ... See more keywords
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Published in 2025 at "Journal of Biochemical and Molecular Toxicology"
DOI: 10.1002/jbt.70443
Abstract: We report the synthesis of four novel monoquaternary salts and four fused pyrrolo‐phenanthridine compounds, fully characterized by NMR, FT‐IR, and mass spectrometry. Guided by theoretical predictions, including molecular docking studies, we assessed their cytotoxic activity…
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Keywords:
potential anticancer;
anticancer;
pyrrolo;
pyrrolo fused ... See more keywords
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Published in 2024 at "ChemistryOpen"
DOI: 10.1002/open.202400140
Abstract: Abstract Three cationic Gold(I)‐NHC complexes with potential anticancer properties were studied using DFT with B3LYP functional in combination with two basis sets, LanL2DZ and SDD. Obtained equilibrium geometries and computed IR spectra were found in…
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Keywords:
anticancer properties;
potential anticancer;
complexes potential;
basis sets ... See more keywords
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Published in 2023 at "Phytotherapy Research"
DOI: 10.1002/ptr.7841
Abstract: Angelica species have been traditionally used for their medicinal properties. Recent studies have suggested their potential use as anticancer agents, making them an area of interest for further research. The review aims to summarize the…
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Keywords:
potential anticancer;
antitumor;
review;
angelica species ... See more keywords
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Published in 2020 at "Molecular Diversity"
DOI: 10.1007/s11030-020-10147-6
Abstract: Abstract In this paper, we report the synthesis of novel hybrids 2–14 based on itaconic acid and fluoroaniline, pyridine, indole and quinoline scaffolds. Itaconic acid is a naturally occurring compound with a Michael acceptor moiety,…
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Keywords:
anticancer agents;
itaconic acid;
acid hybrids;
hybrids potential ... See more keywords
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Published in 2019 at "3 Biotech"
DOI: 10.1007/s13205-019-1718-4
Abstract: Ruthenium seems to be a promising alternative to platinum because of the wide range of oxidation states it has and its ability to form complexes with bioactive ligands. In this study, naringin, a naturally occurring…
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Keywords:
ruthenium;
complex potential;
anticancer applications;
ruthenium complex ... See more keywords
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Published in 2020 at "European journal of medicinal chemistry"
DOI: 10.1016/j.ejmech.2020.113108
Abstract: In this work, we reported the discovery of compound 6i with potent antiproliferative activity against MGC-803. Among these compounds, the most potent compound 6i could effectively inhibit MGC-803 (IC50 = 0.96 μM), being around 38-fold selectivity over GES-1.…
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Keywords:
mgc 803;
discovery triazolo;
triazolo pyrimidines;
derivatives potential ... See more keywords
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Published in 2021 at "European journal of medicinal chemistry"
DOI: 10.1016/j.ejmech.2021.113321
Abstract: β-Carbolines are indole alkaloids having a tricyclic pyrido[3,4-b]indole ring in their structure. Since the isolation of first β-carboline from Peganum harmala in 1841, the isolation and synthesis of various β-carboline derivatives surged in the following…
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Keywords:
carbolines potential;
anticancer agents;
chemistry;
anticancer ... See more keywords
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Published in 2021 at "Journal of medicinal chemistry"
DOI: 10.1021/acs.jmedchem.1c00413
Abstract: Novel dual HDAC3/tubulin inhibitors were designed and efficiently synthesized by combining the pharmacophores of SMART (tubulin inhibitor) and MS-275 (HDAC inhibitor), among which compound 15c was found to be the most potent and balanced HDAC3/tubulin…
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Keywords:
compound 15c;
novel dual;
cancer cell;
tubulin ... See more keywords
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Published in 2021 at "Journal of medicinal chemistry"
DOI: 10.1021/acs.jmedchem.1c00715
Abstract: We previously reported a potent tubulin inhibitor CH-2-77. In this study, we optimized the structure of CH-2-77 by blocking metabolically labile sites and synthesized a series of CH-2-77 analogues. Two compounds, 40a and 60c, preserved…
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Keywords:
tubulin;
binding site;
colchicine binding;
potential anticancer ... See more keywords
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Published in 2022 at "Dalton transactions"
DOI: 10.1039/d2dt00290f
Abstract: The synthesis of new types of mono- and polynuclear ruthenium nitrosyl complexes is driving progress in the field of NO generation for a variety of applications. Light-induced Ru-NO bond dissociation in solution may involve transient…
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Keywords:
potential anticancer;
nitrosyl complexes;
ruthenium nitrosyl;
anticancer drugs ... See more keywords