Zobrazeno 1 - 10
of 402
pro vyhledávání: '"E J, Parish"'
Autor:
Ik-Soo Lee
Publikováno v:
Phytochemical Analysis. 4:293-294
Autor:
T. M. Shead, I. K. Tezaur, W. L. Davis IV, M. L. Carlson, D. M. Dunlavy, E. J. Parish, P. J. Blonigan, J. Tencer, F. Rizzi, H. Kolla
Publikováno v:
Lecture Notes in Energy ISBN: 9783031162473
We present a novel framework for automatically detecting spatial and temporal events of interest in situ while running high performance computing (HPC) simulations. The new framework – composed from signature, measure, and decision building blocks
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2058f31b28b9b8c2e519c3b7110b5e90
https://doi.org/10.1007/978-3-031-16248-0_3
https://doi.org/10.1007/978-3-031-16248-0_3
Publikováno v:
Journal of Lipid Research, Vol 27, Iss 11, Pp 1190-1204 (1990)
Treatment of rat intestinal epithelial cell cultures with the oxidosqualene cyclase inhibitor, 3 beta-[2-(diethylamino)-ethoxy]androst-5-en-17-one (U18666A), resulted in an accumulation of squalene 2,3:22,23-dioxide (SDO). When U18666A was withdrawn
Externí odkaz:
https://doaj.org/article/96c1c06bc0e34a83bb5bc8fa59f2b3ba
Publikováno v:
Journal of Macromolecular Science, Part A. 40:1397-1406
A polymer does not have to be conjugated to become electrically conductive. The correct fundamental basis for a polymer to be conductive is that it must have at least one double bond in the repeat. The magnitude of conductivity increases with the num
Autor:
E J Parish, G J Schroepfer, Jr
Publikováno v:
Journal of Lipid Research, Vol 22, Iss 5, Pp 859-868 (1981)
A simplified method is described for the preparation of 14 alpha-hydroxymethyl-4,4-dimethyl-5 alpha-cholest-8-en-e beta-ol, 14 alpha-hydroxymethyl-4,4-dimethyl-5 alpha-cholest-7-en-3 beta-ol, and 14 alpha-hydroxymethyl-4,4-dimethyl-5-alpha-cholest-6-
Externí odkaz:
https://doaj.org/article/d9eff28e7d374337ba1c3be68a847e6d
Publikováno v:
Journal of Lipid Research, Vol 21, Iss 5, Pp 571-584 (1980)
The chemical syntheses of a number of 14 alpha-hydroxymethyl sterols and 14 alpha -hydroxymethyl-15 alpha-hydroxysterols and their derivatives have been pursued to permit evaluation of their activity in the inhibition of sterol biosynthesis in animal
Externí odkaz:
https://doaj.org/article/69a07bfef8804ffbbb5fac6c0427ece8
Publikováno v:
Journal of Lipid Research, Vol 20, Iss 8, Pp 994-998 (1979)
Reported herein are the results of investigations of the effects of a number of 14 alpha-alkyl-substituted 15-oxygenated sterols, prepared by chemical synthesis, on sterol biosynthesis and the levels of 3-hydroxy-3-methylglutaryl CoA reductase activi
Externí odkaz:
https://doaj.org/article/b77b4c2b728b4e448e3c767634b5dfc9
Publikováno v:
Chemistry and physics of lipids. 109(1)
Reduction of 3beta-benzoyloxy-14alpha,15alpha-epoxy-5alpha-cholest-7-ene with lithium in ethylenediamine gave 5alpha-cholest-8(14)-en-3beta, 5alpha-diol in high yield. This procedure offers an alternate synthesis through the reductive rearrangement o
Autor:
Lee, Ik Soo
Publikováno v:
Phytochemical Analysis; Nov1993, Vol. 4 Issue 6, p293-294, 2p
Publikováno v:
Chemistry and physics of lipids. 74(1)
3 beta-Hydroxy-5 alpha-cholestan-15-one (2a) and its 14 beta-epimer 2b were prepared from 3 beta-acetoxy-5 alpha-cholest-8(14)-ene (3). Hydroboration of 3 at 45-50 degrees C gave a mixture of 5 alpha,14 alpha-cholestane-3 beta,15 alpha-diol and 5 alp