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Alkyl N-Benzylthiocarbamates, the First Copper(II) Ion-Chelating Tyrosinase Inhibitors with a Thiocarbamate Group and ROS-Scavenging Activity, Exhibit Different Inhibitory Activities Depending on the Origin of Tyrosinase [PDF]

open access: goldAntioxidants
N-Benzylthiocarbamate (NBTC) analogs 1–10 were synthesized as potential Cu2+-chelating tyrosinase inhibitors. Most analogs exhibited strong Cu2+-chelating activity, but none inhibited mushroom tyrosinase (mTYR) activity better than kojic acid (KA ...
Hee Jin Jung   +11 more
doaj   +3 more sources

Enantiopure (S)-butan-2-yl N-(4-x-phenyl)thiocarbamates, x = NO2, OCH3, F, and Cl [PDF]

open access: goldActa Crystallographica Section E: Crystallographic Communications, 2023
The structures of (S)-butan-2-yl N-(4-nitrophenyl)thiocarbamate, C11H14N2O3S, (I), (S)-butan-2-yl N-(4-methoxyphenyl)thiocarbamate, C12H17NO2S, (II), (S)-butan-2-yl N-(4-fluorophenyl)thiocarbamate, C11H14FNOS, (III), and (S)-butan-2-yl N-(4-chlorophenyl ...
Werner Kaminsky, Max Kaganyuk
doaj   +4 more sources

A novel three-component reaction between isocyanides, alcohols or thiols and elemental sulfur: a mild, catalyst-free approach towards O-thiocarbamates and dithiocarbamates [PDF]

open access: diamondBeilstein Journal of Organic Chemistry, 2019
A new multicomponent reaction has been developed between isocyanides, sulfur and alcohols or thiols under mild reaction conditions to afford O-thiocarbamates and dithiocarbamates in moderate to good yields.
András György Németh   +2 more
doaj   +2 more sources

Crystal structure of O-ethyl N-(ethoxycarbonyl)thiocarbamate [PDF]

open access: goldActa Crystallographica Section E: Crystallographic Communications, 2015
The title compound, C6H11NO3S, provides entries to novel carbamoyl disulfanes and related compounds of interest to our laboratory. The atoms of the central O(C=S)N(C=O)O fragment have an r.m.s.
Matthew J. Henley   +3 more
doaj   +2 more sources

Thiocarbamates as plant growth regulators [PDF]

open access: bronzePlant Physiology, 1961
The findings of van der Kerk and his coworkers (10) that carboxymethyl (limietlhyldithiocarbamate (1) caused epinastic curvature ancl leaf deformations as well as some elongation of Avena coleoptile tissue related its action as a growth regulator to that of indole-3-acetic acid and other aromatic structures.
Robert Muir   +2 more
openalex   +4 more sources

Structure-guided engineering of molinate hydrolase for the degradation of thiocarbamate pesticides.

open access: goldPLoS ONE, 2015
Molinate is a recalcitrant thiocarbamate used to control grass weeds in rice fields. The recently described molinate hydrolase, from Gulosibacter molinativorax ON4T, plays a key role in the only known molinate degradation pathway ending in the formation ...
José P Leite   +6 more
doaj   +3 more sources

Chitosan-Based Bio-Composite Modified with Thiocarbamate Moiety for Decontamination of Cations from the Aqueous Media [PDF]

open access: goldMolecules, 2020
Herein, we report the development of chitosan (CH)-based bio-composite modified with acrylonitrile (AN) in the presence of carbon disulfide. The current work aimed to increase the Lewis basic centers on the polymeric backbone using single-step three ...
Nisar Ali   +5 more
doaj   +2 more sources

Novel Cholinesterase Inhibitors Based on O-Aromatic N,N-Disubstituted Carbamates and Thiocarbamates [PDF]

open access: goldMolecules, 2016
Based on the presence of carbamoyl moiety, twenty salicylanilide N,N-disubstituted (thio)carbamates were investigated using Ellman’s method for their ability to inhibit acetylcholinesterase (AChE) and butyrylcholinesterase (BChE).
Martin Krátký   +4 more
doaj   +2 more sources

Pesticide Toxicity Profile: Thiocarbamate Fungicides

open access: yesEDIS, 2005
This document provides a general overview of human toxicity, provides a listing of laboratory animal and wildlife toxicities and a cross reference of chemical, common and trade names of thiocarbamate pesticides used as fungicides registered for use in ...
Frederick M. Fishel
doaj   +7 more sources

Synthesis and Photoreactivity of 7-Nitroindoline-S-thiocarbamates. [PDF]

open access: goldACS Omega, 2023
Baily PT   +12 more
europepmc   +3 more sources

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