Results 21 to 30 of about 14,086 (252)

Designing Tailored Thiosemicarbazones with Bespoke Properties: The Styrene Moiety Imparts Potent and Selective Anti-Tumor Activity [PDF]

open access: yes, 2023
Background: Thiosemicarbazones of the di-2-pyridylketone thiosemicarbazone class possess potent anti-tumor activity via binding essential metal ions in cancer cells (e.g., iron (Fe(II)), copper (Cu(II)), and zinc (Zn(II)) to form metal complexes.
Dharmasivam, Mahendiran   +2 more
core   +1 more source

Designing Tailored Thiosemicarbazones with Bespoke Properties: The Styrene Moiety Imparts Potent Activity, Inhibits Heme Center Oxidation, and Results in a Novel "Stealth Zinc(II) Complex".

open access: yesJournal of Medicinal Chemistry, 2023
A novel, potent, and selective antitumor agent, namely (E)-3-phenyl-1-(2-pyridinyl)-2-propen-1-one 4,4-dimethyl-3-thiosemicarbazone (PPP44mT), and its analogues were synthesized and characterized and displayed strikingly distinctive properties.
M. Dharmasivam   +8 more
semanticscholar   +1 more source

Pyridine-Based NNS Tridentate Chitosan Thiosemicarbazones and Their Copper(II) Complexes: Synthesis, Characterization, and Anticancer Activity

open access: yesACS Omega, 2022
Chitosan-functionalized pyridine-based thiosemicarbazones and their copper(II) complexes have been found to own a substantial antiproliferative activity against the tumorigenic Madin Darby canine kidney (MDCK) and MCF-7 cancer cell lines.
Hari Sharan Adhikari   +3 more
semanticscholar   +1 more source

Thiosemicarbazones as versatile photoswitches with light-controllable supramolecular activity. [PDF]

open access: yesChem Sci
Using photoswitchable molecules to manipulate supramolecular interactions under light illumination has driven advancements in numerous fields, allowing for the strategic alteration of molecular systems.
Sentürk B, Butschke B, Eisenreich F.
europepmc   +3 more sources

Rhodium Assisted C−H Activation of Benzaldehyde Thiosemicarbazones and Their Oxidation via Activation of Molecular Oxygen [PDF]

open access: yes, 2016
The benzaldehyde thiosemicarbazones are found to undergo oxidation at the sulfur center upon reaction with [Rh(PPh3)3Cl] in refluxing ethanol in the presence of a base (NEt3).
Shie-Ming Peng (1425703)   +6 more
core   +9 more sources

Steric Blockade of Oxy-Myoglobin Oxidation by Thiosemicarbazones: Structure–Activity Relationships of the Novel PPP4pT Series [PDF]

open access: yes, 2023
The di-2-pyridylketone thiosemicarbazones demonstrated marked anticancer efficacy, prompting progression of DpC to clinical trials. However, DpC induced deleterious oxy-myoglobin oxidation, stifling development.
Bernhardt, Paul V   +12 more
core   +1 more source

Novel Thiosemicarbazones Sensitize Pediatric Solid Tumor Cell-Types to Conventional Chemotherapeutics through Multiple Molecular Mechanisms [PDF]

open access: yes, 2020
Combining low-dose chemotherapies is a strategy for designing less toxic and more potent childhood cancer treatments. We examined the effects of combining the novel thiosemicarbazones, di-2-pyridylketone 4-cyclohexyl-4-methyl-3-thiosemicarbazone (DpC ...
Jakub Neradil   +15 more
core   +1 more source

SYNTHESIS, CHARACTERIZATION AND THERMAL STUDIES OF MIXED LIGAND COMPLEXES OF Hg(II) THIOSEMICARBAZONES WITH 2-AMINOTHIAZOLE [PDF]

open access: yesBulletin of Pharmaceutical Sciences. Assiut University, 2009
Several Hg(II) mixed ligand complexes of thiosemicarbazones (2-acetylpyridine-, 4-aminoacetophenone- and 2-furaldehyde thiosemicarbazones) with 2-aminothiazole have beenprepared.
Kamal Al-Jadabi
doaj   +1 more source

Monosubstituted Acetophenone Thiosemicarbazones as Potent Inhibitors of Tyrosinase: Synthesis, Inhibitory Studies, and Molecular Docking

open access: yesPharmaceuticals, 2021
A set of 12 monosubstituted acetophenone thiosemicarbazone derivatives (TSCs) were synthesized and their inhibitory properties toward tyrosinase activity were tested.
Katarzyna Hałdys   +4 more
doaj   +1 more source

Synthesis, characterization and antiproliferative activity of hexa arm star shaped thiosemicarbazones derived from cyclotriphosphazene core [PDF]

open access: yes, 2014
A series of novel hexa-arm star shaped thiosemicarbazones with different substitutions at para positions emanating from cyclotriphosphazene core were prepared with excellent yields.
Patil, B.R.   +5 more
core   +1 more source

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