Results 41 to 50 of about 14,086 (252)

Anticancer Thiosemicarbazones: Chemical Properties, Interaction with Iron Metabolism, and Resistance Development

open access: yesAntioxidants and Redox Signaling, 2018
Significance: During the past decades, thiosemicarbazones were clinically developed for a variety of diseases, including tuberculosis, viral infections, malaria, and cancer.
P. Heffeter   +5 more
semanticscholar   +1 more source

Tripeptides conjugated with thiosemicarbazones: new inhibitors of tyrosinase for cosmeceutical use

open access: yesJournal of Enzyme Inhibition and Medicinal Chemistry, 2023
The development of skin-care products is recently growing. Cosmetic formulas containing active ingredients with proven efficacy, namely cosmeceuticals, are based on various compounds, including peptides.
Patrycja Ledwoń   +8 more
doaj   +1 more source

Novel isatin–triazole based thiosemicarbazones as potential anticancer agents: synthesis, DFT and molecular docking studies

open access: yesRSC Advances
Thiosemicarbazones of isatin have been found to exhibit versatile bioactivities. In this study, two distinct types of isatin–triazole hybrids 3a and 3b were accessed via copper-catalyzed azide–alkyne cycloaddition reaction (CuAAC), together with their ...
A. Mushtaq   +3 more
semanticscholar   +1 more source

A review of recent research on the antimicrobial activities of thiosemicarbazone-based compounds

open access: yesJournal of New Results in Science
Thiosemicarbazones can be synthesized by condensation of thiosemicarbazides with ketones or aldehydes and play a role as precursors in the synthesis of many compounds such as thiazoles.
Gürsel Korkmaz
doaj   +1 more source

COMPUȘI COORDINATIVI AI CUPRULUI(II) CU TIOSEMICARBAZONE ALE 2-FORMILPIRIDINEI ȘI DERIVAȚILOR EI

open access: yesStudia Universitatis Moldaviae: Stiinte reale si ale naturii, 2021
În articol este efectuată analiza literaturii de specialitate privind sinteza, caracterizarea structurală și proprietățile bio­lo­gice ale compușilor coordinativi ai cuprului(II) în baza tiosemicarbazonelor 2-formilpiridinei și a derivaților ei.
Elena NEGUȚA
doaj  

Development of pyridyl thiosemicarbazones as highly potent agents for the treatment of malaria after oral administration [PDF]

open access: yes, 2019
Objectives: Drug resistance exists to all current and investigational antimalarial drug classes. Consequently, we have set out to develop chemically and mechanistically discrete antimalarials.
Chavchich, Marina   +7 more
core   +1 more source

Thiosemicarbazones suppress expression of the c-Met oncogene by mechanisms involving lysosomal degradation and intracellular shedding [PDF]

open access: yes, 2020
Considering the role of proto-oncogene c-Met (c-Met) in oncogenesis, we examined the effects of the metastasis suppressor, N-myc downstream-regulated gene-1 (NDRG1), and two NDRG1-inducing thiosemicarbazone-based agents, Dp44mT and DpC, on c-Met ...
Geleta, B   +7 more
core   +1 more source

IN VITRO study of copper coordination compounds with thiosemicarbazone action on antioxidant enzymes

open access: yesOne Health & Risk Management
Introduction. Thiosemicarbazones represent a class of organic compounds with significant pharmacological potential, known for their antitumor, antimicrobial, and antiviral activities.
Valeriana PANTEA   +4 more
doaj   +1 more source

Influence of the Reaction Conditions in the Crystal Structures of Zn(II) and Ni(II) Coordination Compounds with a Dissymmetric Bis(Thiosemicarbazone) Ligand

open access: yesCrystals, 2022
The new ligand HMeATSM, derived from condensation of 2-3-butanedione with 4-methyl-3-thiosemicarbazide and 2,4-dimethyl-3-thiosemicarbazide, has been synthesized.
Luis Alonso   +3 more
doaj   +1 more source

Potential leishmanicidal of the thiosemicarbazones: A review

open access: yesResults in Chemistry
Thiosemicarbazones constitute a class of organic compounds with the general structure R=N-NH-CS-NHR and are known for their biological properties, making them an important structure for drug development. This work presents a systematic review of the main
Edilane Almeida da Silva   +5 more
doaj   +1 more source

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