Results 31 to 40 of about 46,055 (292)

Pyridinium-2-carbaldoximes with quinolinium carboxamide moiety are simultaneous reactivators of acetylcholinesterase and butyrylcholinesterase inhibited by nerve agent surrogates

open access: yesJournal of Enzyme Inhibition and Medicinal Chemistry, 2021
The pyridinium-2-carbaldoximes with quinolinium carboxamide moiety were designed and synthesised as cholinesterase reactivators. The prepared compounds showed intermediate-to-high inhibition of both cholinesterases when compared to standard oximes. Their
Hyun Myung Lee   +13 more
doaj   +1 more source

Novel Tryptanthrin Derivatives with Selectivity as c–Jun N–Terminal Kinase (JNK) 3 Inhibitors

open access: yesMolecules, 2023
The c-Jun N-terminal kinase (JNK) family includes three proteins (JNK1-3) that regulate many physiological processes, including cell proliferation and differentiation, cell survival, and inflammation.
Igor A. Schepetkin   +8 more
doaj   +1 more source

Functionalised oximes : emergent precursors for carbon-, nitrogen- and oxygen-centred radicals [PDF]

open access: yes, 2016
The author thanks EaStCHEM for financial support.Oxime derivatives are easily made, are non-hazardous and have long shelf lives. They contain weak N–O bonds that undergo homolytic scission, on appropriate thermal or photochemical stimulus, to initially ...
John C. Walton   +3 more
core   +1 more source

The Evaluation of the Reactivating and Neuroprotective Efficacy of Two Newly Prepared Bispyridinium Oximes (K305, K307) in Tabun-Poisoned Rats—A Comparison with Trimedoxime and the Oxime K203

open access: yesMolecules, 2017
The ability of two newly developed oximes (K305, K307) to protect tabun-poisoned rats from tabun-induced inhibition of brain acetylcholinesterase, acute neurotoxic signs and symptoms and brain damage was compared with that of the oxime K203 and ...
Jiri Kassa   +6 more
doaj   +1 more source

Cytotoxic and genotoxic effects of oxime β-lapachone in human cancer cells: selectivity toward NCI-H460 and insights from molecular docking [PDF]

open access: hybridHum Cell
Maria Francilene Souza Silva   +14 more
openalex   +2 more sources

Photochemical e-z isomerisation and cyclisation in an arylidenecycloakanone oxime ether system [PDF]

open access: yes, 1994
The synthesis and photochemistry of a number of arylidenecycloalkanone oxime ethers has been investigated . Irradiation of E,E- 2-benzylidenecyclopentanone oxime O-allyl ether results in rapid E-Z isomérisation around the carbon-nitrogen double bond ...
Austin, Mark
core   +2 more sources

The Separation of Cobalt by Solvent Extraction Using Oxime-Amine Mixture System

open access: yesJournal of MMIJ, 2017
Extraction behavior of cobalt from sulfate media containing excess manganese by mixtures LIX63 and several amines was investigated. The addition of amines shifted cobalt extraction isotherm to higher pH region in all case.
Masatoshi TAKANO   +5 more
doaj   +1 more source

Manganese Catalyzed Oximation of Hydrocarbons to Oximes

open access: yesNature Communications
Abstract Oximes are used in many scientific and industrial domains, ranging from organic synthesis through biotechnology to materials science. Traditionally, their synthesis necessitates the use of hydrocarbons with specific functional groups, such as carbonyls, which are often more challenging and expensive to obtain compared to their ...
Menghui Song   +10 more
openaire   +2 more sources

Novel Group of AChE Reactivators—Synthesis, In Vitro Reactivation and Molecular Docking Study

open access: yesMolecules, 2018
The acetylcholinesterase (AChE) reactivators (e.g., obidoxime, asoxime) became an essential part of organophosphorus (OP) poisoning treatment, together with atropine and diazepam.
David Malinak   +4 more
doaj   +1 more source

Oximes: Novel Therapeutics with Anticancer and Anti-Inflammatory Potential

open access: yesBiomolecules, 2021
Oximes have been studied for decades because of their significant roles as acetylcholinesterase reactivators. Over the last twenty years, a large number of oximes have been reported with useful pharmaceutical properties, including compounds with ...
Igor A. Schepetkin   +4 more
doaj   +1 more source

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