Zobrazeno 1 - 10
of 17
pro vyhledávání: '"David J. Sellers"'
Autor:
Christopher M. Timperley, David J. Sellers, Stuart Notman, Krystal E. Casey, Gareth R. Williams, Nancy E. Williams, Nichola H. Williams
Publikováno v:
Journal of Fluorine Chemistry. 127:1554-1563
Eighteen new fluorogenic analogues of organophosphorus nerve agents were synthesised and characterised. They included analogues of tabun, sarin, cyclosarin, soman, VX, and Russian VX, with the 7-oxy-4-methylcoumarin or 7-oxy-4-(trifluoromethyl)coumar
Autor:
Michael Bird, David J. Sellers, Malcolm W. Parry, Robert E. Arbon, Colin R. Willis, Stuart Anson Brewer, Christopher M. Timperley
Publikováno v:
Journal of Fluorine Chemistry. 121:23-31
Ten fluoromonomers of structure (RFO)2P(O)OCH2CH2OC(O)CRCH2 were made in 30–64% yield by treating the chloridates (RFO)2P(O)Cl with HOCH2CH2OC(O)CRCH2 in chloroform in the presence of triethylamine [RF=CF3CH2, C2F5CH2, C3F7CH2, C4F9CH2, C4F9C
Publikováno v:
Journal of Fluorine Chemistry. 107:155-158
Whilst examining the chemistry of a series of tris(fluoroalkyl) phosphates as potential fire retardants, concern was raised over their possible anticholinesterase activity. Bimolecular rate constants ( k i values) for the inhibition of bovine erythro
Autor:
James Hill, Janet Wetherell, and Alan R. Fersht, Christopher M. Timperley, Gareth R. Williams, Andrew D. Griffiths, Stuart Notman, Andy P. Smith, Nichola H. Williams, Luis Briseño-Roa, David J. Sellers
Publikováno v:
Journal of medicinal chemistry. 49(1)
Enzymes that efficiently hydrolyze highly toxic organophosphorus nerve agents could potentially be used as medical countermeasures. As sufficiently active enzymes are currently unknown, we synthesized twelve fluorogenic analogues of organophosphorus
Publikováno v:
Biochemical Pharmacology. 35:745-751
The y in vitro reactivation profiles of O , O -diethyl phosphorylated ACh E and O -ethyl methyl phosphonylated AChE by P2S (2-hydroxy iminomethyl-1-methyl-pyridinium methane sulphonate) have been determined. Whilst reinhibition of the reactivated ACh
Autor:
D. G. Upshall, M. C. French, David J. Sellers, C. R. Hall, Thomas D. Inch, Andrew P. Smith, J. M. Harrison, P. Watts
Publikováno v:
Pesticide Biochemistry and Physiology. 24:53-60
R (+)-Ethyl S -propyl methylphosphonothioate is bioactivated both in vivo and when perfused through isolated liver to give a product which is much more active as an inhibitor of acetylcholinesterase than the parent compound. The bioactivation does no
Publikováno v:
Biochemical Pharmacology. 35:737-744
The rates of formation and decomposition of a series of phosphylated oximes derived from P2S (2-hydroxy-iminomethyl-1-methylpyridinium methane-sulphonate) have been measured. The rates of inhibition of AChE by these phosphylated oximes and the parent
Publikováno v:
Biochemical Pharmacology. 32:787-793
A study of the mechanism of interaction of acetylcholinesterase with some simple tetra-N-alkyammonium ions has been made. Kinetic schemes have been proposed which are consistent with the experimental results observed in the enzyme-tetra-N-alkylammoni
Publikováno v:
International Journal of Clinical and Experimental Hypnosis. 16:26-37
The probability that hypnotic induction produces psycho-pathological effects has not been experimentally determined. The present study hypothesizes various negative effects following hypnosis such as increased signs of personality disturbances, incre
Publikováno v:
Tetrahedron Letters. 12:2329-2332