Results 81 to 90 of about 10,379 (265)

hydrazonic acids [PDF]

open access: yes, 2014
Citation: 'hydrazonic acids' in the IUPAC Compendium of Chemical Terminology, 3rd ed.; International Union of Pure and Applied Chemistry; 2006. Online version 3.0.1, 2019. 10.1351/goldbook.H02885 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
openaire   +2 more sources

An overview on synthetic aspects and biological activity profiles of hydrazone derivatives

open access: yesDiscover Chemistry
In the realm of medicinal chemistry, hydrazide-hydrazones represent a versatile class of compounds that have attracted significant attention due to their structural flexibility with respect to molecular design and wide-ranging biological activities ...
K. Nagaraj Pai, K. Subrahmanya Bhat
doaj   +1 more source

Synthesis, Cytotoxicity and Antiproliferative Effect of New Pyrrole Hydrazones

open access: yesMolecules
Novel pyrrole-based carbohydrazide (1) and hydrazones (1A–D) were synthesized, characterized, and subjected to spectroscopic studies. The hydrazones were obtained by reacting a pyrrole hydrazide with substituted pyrrole aldehydes.
Stanislava Vladimirova   +2 more
doaj   +1 more source

Design, Synthesis and Evaluation of Antiproliferative Activity of New Benzimidazolehydrazones

open access: yesMolecules, 2016
The synthesis and antiproliferative activity of new benzimidazole derivatives bearing an hydrazone mojety at the 2-position is described. The new N′-(4-arylidene)-1H-benzo[d]imidazole-2-carbohydrazides were evaluated for their cytostatic activity toward ...
Valentina Onnis   +8 more
doaj   +1 more source

Novel sulindac derivatives: synthesis, characterisation, evaluation of antioxidant, analgesic, anti-inflammatory, ulcerogenic and COX-2 inhibition activity

open access: yesJournal of Enzyme Inhibition and Medicinal Chemistry, 2020
A new series of N′-(substituted phenyl)-2-(1-(4-(methylsulfinyl) benzylidene)−5-fluoro-2-methyl-1H-inden-3-yl) acetohydrazide derivatives (1 – 25) were prepared in good yields in an efficient manner.
Mashooq A. Bhat   +7 more
doaj   +1 more source

Hydrazones, hydrazones-based coinage metal complexes, and their biological applications

open access: yesRSC Advances
Hydrazone-based compounds distinguished by their azomethine –NHNCH group and their respective coinage metal complexes have emerged as leading candidates in the search for effective anticancer and antibiotic agents.
Dessie Ashagrie Tafere   +6 more
openaire   +2 more sources

Metal-catalyzed fluoroalkylation of hydrazones

open access: yes, 2016
La chimie du fluor suscite un intérêt croissant de la part des chimistes organiciens de par son exploitation industrielle dans les domaines pharmaceutique et agrochimique.
Prieto, Alexis
core  

Analysis and Characterization of Kisspeptin and Its Analogues in Serum and Urine Samples by Liquid Chromatography–High‐Resolution Mass Spectrometry for Doping Control Purposes

open access: yesDrug Testing and Analysis, EarlyView.
Sensitive LC‐HRMS methods were established for the detection of kisspeptin and its analogues in serum and urine, alongside their analytical and metabolic characterization. Stability studies were conducted in serum, plasma, and urine, highlighting the importance of appropriate sample handling for reliable anti‐doping analysis.
Sophia Krombholz   +3 more
wiley   +1 more source

Antimalarial Activity of Small-Molecule Benzothiazole Hydrazones

open access: yes, 2016
We synthesized a new series of conjugated hydrazones that were found to be active against malaria parasite in vitro as well as in vivo in murine model. These hydrazones concentration-dependently chelated free iron and offered antimalarial activity.
Siddiqui, Asim A.   +9 more
core   +1 more source

Detection of Testosterone Esters in Urine: Evidence of Trace‐Level Detectability in Doping Control Samples

open access: yesDrug Testing and Analysis, EarlyView.
An ultrasensitive LC‐MS/MS method for detecting testosterone esters (T‐esters) in urine at sub–pg/mL levels is presented. This approach, employing Girard P derivatization, provides the first evidence of T‐esters' trace‐level detectability in human urine.
Daniel Pecher   +3 more
wiley   +1 more source

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