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41.
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V. V. Klochkov Sh. K. Latypov L. K. Yuldasheva A. V. Aganov A. V. Il'yasov B. A. Arbuzov 《Russian Chemical Bulletin》1987,36(3):496-499
Conclusions From an analysis of the variation of1 H NMR spectra with temperature it has been shown that 2-substituted 5,6-benz-1,3-dithiepins exist in solution in the chair-e and boat-e conformations, the equilibrium between which depends considerably on the nature of the solvent.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 545–548, March, 1987.The authors wish to thank E. N. Klimovitskii and D. Yu. Strel'nik for submitting compound (III). 相似文献
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L. N. Yuldasheva A. Cruz e Carvalho O. V. Krasilnikov 《Journal of inclusion phenomena and macrocyclic chemistry》2008,60(1-2):65-70
It is believed that the biological effects of chelating agents such as crown ethers are largely related to their ability to
form complexes with ions and/or to facilitate ion transport across membranes. Specific influences are rarely related. Here
we present the evidence that even one of the simplest representatives of the crown ether super-family, 1,4,7,10,13,16-hexaoxacyclooctane
(18-crown-6), is able to affect the activity of Na+, K+-ATPase directly. Using nonlinear regression fitting to kinetic data we have found that the crown ether diminishes the apparent
Michaelis constant, K
m
, and the maximal rate of ATP hydrolysis, V
m
, acting as noncompetitive inhibitors. The apparent dissociation constants, K
i
, for the crown interaction with the free ATPase and with the enzyme-substrate complex were established to be of 77 ± 3 mM
and 21 ± 2 mM, respectively. So 18-crown-6 possesses weak but “direct” pharmacological activity on Na+, K+-ATPase hinders the formation of enzyme–substrate complex and detains the enzyme in this state. 相似文献
49.
Institute of the Chemistry of Plant Substances, Uzbek SSR Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh
Soedinenii, No. 4, pp. 588–589, July–August, 1988. 相似文献
50.