Results 171 to 180 of about 24,863 (212)

Open-Source System Suitability: Mass Spectrometry Query Language Lab (MassQLab). [PDF]

Rapid Commun Mass Spectrom
Winter HL, Johnson D, Jarmusch AK.
europepmc   +1 more source

Trimethylamin aus Menschenharn [PDF]

Justus Liebigs Annalen der Chemie
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Gut Microbiome and Cardiovascular Health: Mechanisms, Therapeutic Potential and Future Directions. [PDF]

Heart Int
Edpuganti S, Subhash S, Subrahmaniyan SL, Latheef S, Albarari SS.   +4 more
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All Roads Lead to Carbinolamine: QM/MM Study of Enzymatic C-N Bond Cleavage in Anaerobic Glycyl Radical Enzyme Choline Trimethylamine-Lyase (CutC). [PDF]

J Phys Chem B
Hanzevacki M, Güven JJ, Hinchliffe P, Shaw J, Mey ASJS, Fey N, Spencer J, Mulholland AJ.   +7 more
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Research Trends and Hotspots of Gut Microbiota and Its Metabolites in Cardiovascular Diseases: A Bibliometric Analysis. [PDF]

J Multidiscip Healthc
Zhang K, Shi Y, Peng L, Zhang X, Zheng N, Xin J, Zou J, Luan F.   +7 more
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Dietary Fatty Acids Modulate Gut Microbiota-Derived Trimethylamine-N-Oxide: Potential Mechanisms and Future Perspective. [PDF]

Nutrients
Kilic E, Basaran P.
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Trimethylamine N-oxide (TMAO) as a prognostic marker among patients at nutritional risk

Schuetz P, Stern A, Wunderle C, Tribolet P, Neyer P, Bernasconi L, Stanga Z, Mueller B.   +7 more
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Pentacarbonyl(trimethylamine)chromium and Pentacarbonyl(trimethylamine)Molybdenum

Journal of Chemical Crystallography, 2009
Pentacarbonyl(trimethylamine)chromium (1) and pentacarbonyl(trimethylamine)molybdenum (2) are isomorphous and crystallize in the space group P21/n, a = 6.8267(14) A, b = 11.269(2) A, c = 14.692(3) A, β = 102.89(3)°, V = 1,101.8(4) A3, Z = 4 for 1 and a = 6.949(5) A, b = 11.362(5) A, c = 14.927(5) A, β = 102.639(5)°, V = 1,150.0(10) A3, Z = 4 for 2 ...
Michael Findlater, Nicholas J. Hill, Alan H. Cowley   +2 more
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Chlorination of trimethylamine borane. Synthesis of trimethylamine dichloroborane

Inorganica Chimica Acta, 1970
Abstract Trimethylamine borane can be chlorinated with a variety of halides and oxyhalides under mild conditions. Reactivity decreases in the order SbCl5∼ SO2Cl2 > SbCl3 > SOCl2 > HgCl2 > HCl > (CH3)3 NH . HCl, and correlates well with thermodynamic properties of the halogenating agents.
J.W. Wiggins, G.E. Ryschkewitsch
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