scholarly journals Raw nuclear magnetic resonance data of human linker histone H1x, lacking the C-terminal domain (NGH1x), and trajectory data of nanosecond molecular dynamics simulations of GH1x- and NGH1x-chromatosomes

Data in Brief ◽  
2020 ◽  
Vol 31 ◽  
pp. 105865
Author(s):  
Herna de Wit ◽  
Alicia Vallet ◽  
Bernhard Brutscher ◽  
Leon du Preez ◽  
Gerrit Koorsen
Keyword(s):  
Molecular Dynamics ◽  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Molecular Dynamics Simulations ◽  
Linker Histone ◽  
Nuclear Magnetic Resonance Data ◽  
Trajectory Data ◽  
Magnetic Resonance Data ◽  
Resonance Data ◽  
Dynamics Simulations

Methods to Determine Phytopharmaceuticals in Tobacco and Tobacco Products. 4th Report: A Procedure to Determine Vamidothion and its Metabolites/Methoden zur Bestimmung von Phytopharmaka in Tabak und Tabakerzeugnissen: IV. Mitteilung: Ein Bestimmungsverfahren fuer Vamidothion und seine Metaboliten

1977 ◽  
Vol 9 (2) ◽  
Author(s):  
A.N. Sagredos ◽  
R. Moser
Keyword(s):  
Mass Spectrometry ◽  
Nuclear Magnetic Resonance ◽  
Acetic Acid ◽  
Magnetic Resonance ◽  
Aluminium Oxide ◽  
Nuclear Magnetic Resonance Data ◽  
Gas Chromatograph ◽  
Tobacco Products ◽  
Magnetic Resonance Data ◽  
Resonance Data

AbstractBased on previous work (7) a method to simultaneously determine vamidothion [I], vamidothion-sulfoxide [II] and vamidothion sulfone [III] in tobacco has been developed. The compounds are extracted with water/acetone/acetic acid from the tobacco, cleansed over an aluminium oxide column and then determined on the gas chromatograph with the specific sulphur detector. Rates of recovery are 70 % - 92 %, the determination level is 0.1 ppm. Mass spectrometry and nuclear magnetic resonance data of vamidothion [I], vamidothion-sulfoxide [ II ] and vamidothion-sulfone [III] are given.

Sign in / Sign up

Export Citation Format

Share Document