Pyridine derivatives as biologically active precursors; organics and selected coordination complexes
E Khan - ChemistrySelect, 2021 - Wiley Online Library
Pyridine (py) is an important heterocyclic compound and is an integral part of various natural
products. There are various medicines containing py ring system being available in the …
products. There are various medicines containing py ring system being available in the …
Thiosemicarbazones as potent anticancer agents and their modes of action
Thiosemicarbazones (TSCs) are a class of Schiff bases usually obtained by the
condensation of thiosemicarbazide with a suitable aldehyde or ketone. TSCs have been the …
condensation of thiosemicarbazide with a suitable aldehyde or ketone. TSCs have been the …
New azafluorenones with cytotoxic and carbonic anhydrase inhibitory properties: 2-Aryl-4-(4-hydroxyphenyl)-5H-indeno [1, 2-b] pyridin-5-ones
Abstract New azafluorenones, 2-aryl-4-(4-hydroxyphenyl)-5H-indeno [1, 2-b] pyridin-5-ones,
were prepared to evaluate their cytotoxic/anticancer properties, also their inhibitory effects …
were prepared to evaluate their cytotoxic/anticancer properties, also their inhibitory effects …
[HTML][HTML] Discovery of novel indene-based hybrids as breast cancer inhibitors targeting Hsp90: Synthesis, bio-evaluation and molecular docking study
AM Alosaimy, AS Abouzied, AMR Alsaedi… - Arabian Journal of …, 2023 - Elsevier
Inhibition of Heat-shock protein 90 (Hsp90) is considered an attractive route in fighting
against cancer proliferation. Herein, new indene derivatives targeting Hsp90 were …
against cancer proliferation. Herein, new indene derivatives targeting Hsp90 were …
Synthesis of mono Mannich bases of 2-(4-hydroxybenzylidene)-2, 3-dihydroinden-1-one and evaluation of their cytotoxicities
Chalcones and Mannich bases are a group of compounds known for their cytotoxicities. In
this study restricted chalcone analogue, compound 2-(4-hydroxybenzylidene)-2, 3 …
this study restricted chalcone analogue, compound 2-(4-hydroxybenzylidene)-2, 3 …
DNA binding and Topoisomerase inhibition: How can these mechanisms be explored to design more specific anticancer agents?
SMV de Almeida, AG Ribeiro, GC de Lima Silva… - Biomedicine & …, 2017 - Elsevier
DNA is considered one of the most promising targets of molecules with anticancer activity
potential. Its key role in various cell division mechanisms, which commands the intense …
potential. Its key role in various cell division mechanisms, which commands the intense …
Discovery and structure-activity relationship studies of 2-benzylidene-2, 3-dihydro-1H-inden-1-one and benzofuran-3 (2H)-one derivatives as a novel class of potential …
To develop effective therapeutics for inflammatory bowel disease (IBD), 2-benzylidene-2, 3-
dihydro-1 H-inden-1-one and benzofuran-3 (2H)-one derivatives, were designed and …
dihydro-1 H-inden-1-one and benzofuran-3 (2H)-one derivatives, were designed and …
Overview of the New Bioactive Heterocycles as Targeting Topoisomerase Inhibitors Useful Against Colon Cancer
MB Santos… - Anti-Cancer Agents …, 2024 - ingentaconnect.com
Colorectal cancer (CRC) is the third most common cancer globally, with high mortality.
Metastatic CRC is incurable in most cases, and multiple drug therapy can increase patients' …
Metastatic CRC is incurable in most cases, and multiple drug therapy can increase patients' …
Stereoselective synthesis of 11-phenylundeca-5Z, 9Z-dienoic acid and investigation of its human topoisomerase I and IIα inhibitory activity
VA D'yakonov, LU Dzhemileva, AA Makarov… - Bioorganic & Medicinal …, 2015 - Elsevier
Abstract (5Z, 9Z)-11-Phenylundeca-5, 9-dienoic acid was stereoselectively synthesized,
based on original cross-cyclomagnesiation of 2-(hepta-5, 6-dien-1-yloxy) tetrahydro-2H …
based on original cross-cyclomagnesiation of 2-(hepta-5, 6-dien-1-yloxy) tetrahydro-2H …
Topoisomerase I and II inhibitory activity, cytotoxicity, and structure–activity relationship study of dihydroxylated 2, 6-diphenyl-4-aryl pyridines
A new series of thirty-six dihydroxylated 2, 6-diphenyl-4-aryl pyridines containing hydroxyl
groups at the ortho, meta, or para position of 2-and 6-phenyl rings attached to the central …
groups at the ortho, meta, or para position of 2-and 6-phenyl rings attached to the central …