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]
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]
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]
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]
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]
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.
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]
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]
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
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]
Baily PT +12 more
europepmc +3 more sources

