Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Rodney G. Wilkinson"'
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:
Acta Chemica Scandinavica. 26:1671-1679
Publikováno v:
Acta Chemica Scandinavica. 26:1527-1541
Publikováno v:
Chemischer Informationsdienst. 6
Publikováno v:
Biochemical pharmacology. 26(13)
An unambiguous method based on the measurement of the acetylcholinesterase activity resulting from complete decarbamoylation of the acetylcholinesterase in blood samples inhibited by a carbamate is described and compared with a spectrophotometric mod
Autor:
D.B. Coult, Rodney G. Wilkinson
Publikováno v:
Biochemical pharmacology. 26(9)
4-Alkyl-2,6,7-trioxa-1-phosphabicyclo [2,2,2] octanes are weak competitive inhibitors of the high- K m form of cyclic adenosine 3′,5′-monophosphate phosphodiesterase (PDE) and non-competitive inhibitors of the low- K m form enzyme. The possibilit
Autor:
P. Watts, Rodney G. Wilkinson
Publikováno v:
Biochemical pharmacology. 26(8)
It has been shown that the kinetic schemes proposed by earlier workers to describe the reactions of carbamates with acetylcholinesterase are incomplete. A reaction scheme has been developed and tested by the use of methyl- and dimethyl-carbamoylcholi
Publikováno v:
Chemischer Informationsdienst. 7
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :1090
The kinetics of the displacement of halide from benzyl fluoride, chloride, and bromide by alkali-metal 9-cyano-, 9-methoxycarbonyl-, and 9-phenylsulphonylfluorenides have been studied in t-butyl alcohol solution in which the salts have been shown to
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :500
Whereas most phosphono-derivatives are hydrolysed more rapidly by hydroxide than the corresponding phosphoro-derivatives, the reverse situation holds for S-alkyl phosphonothioates and S-alkyl phosphorothioates; this reversal of the more usual pattern