Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Jiang Ji-Long"'
Publikováno v:
Polymer. 37:5059-5067
The reactions of 4-bromobutyric acid, 5-bromopentanoic acid, 6-bromohexanoic acid, 8-bromo-octanoic acid, 11-bromoundecanoic acid and 12-methanesulfonyloxydodecanoic acid with the bicarbonate forms of various anion-exchange resins were investigated.
Autor:
A. M. Van Rhee, Neli Melman, Kenneth A. Jacobson, Jiang Ji-Long, Gary L. Stiles, Mark E. Olah
Publikováno v:
Journal of Medicinal Chemistry. 39:2980-2989
1,4-Dihydropyridine and pyridine derivatives bound to three subtypes of adenosine receptors in the micromolar range. Affinity was determined in radioligand binding assays at rat brain A1 and A2A receptors using [3H]-(R)-PIA [[3H]-(R)-N6-(phenylisopro
Publikováno v:
Tetrahedron Letters. 34:261-264
A short synthesis of 2, 3-dideoxy-3(S)-C-hydroxymethyl rebosides is described. The key step involves a photochemical ring-expansion of a chiral cyclobutanone which occurs stereospecifically.
Publikováno v:
ChemInform. 28
An approach to designing dihydropyridines that bind to adenosine receptors without binding to L-type calcium channels has been described. 1,4-Dihydropyridine derivatives substituted with beta-styryl or phenylethynyl groups at the 4-position and aryl
Autor:
Mark E. Olah, Kenneth A. Jacobson, Jiang Ji-Long, Yishai Karton, X. Ji, Gary L. Stiles, Neli Melman
Publikováno v:
ChemInform. 27
A broad screening of phytochemicals has demonstrated that certain flavone and flavonol derivatives have a relatively high affinity at A3 adenosine receptors, with Ki values of > or = 1 microM (Ji et al. J. Med. Chem. 1996, 39, 781-788). We have furth
The adenosine A3 receptor is expressed in brain, but the consequences of activation of this receptor on electrophysiological activity are unknown. We have characterized the actions of a selective adenosine A3 receptor agonist, 2-chloro-N6-(3-lodobenz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::170f7b8aedb956af44b1e2a0251313e5
https://europepmc.org/articles/PMC5470729/
https://europepmc.org/articles/PMC5470729/
Publikováno v:
Journal of medicinal chemistry. 39(23)
An approach to designing dihydropyridines that bind to adenosine receptors without binding to L-type calcium channels has been described. 1,4-Dihydropyridine derivatives substituted with beta-styryl or phenylethynyl groups at the 4-position and aryl
Autor:
Jiang Ji-Long, Neli Melman, Mark E. Olah, Kenneth A. Jacobson, X. Ji, Yishai Karton, Gary L. Stiles
Publikováno v:
Journal of medicinal chemistry. 39(12)
A broad screening of phytochemicals has demonstrated that certain flavone and flavonol derivatives have a relatively high affinity at A3 adenosine receptors, with Ki values of > or = 1 microM (Ji et al. J. Med. Chem. 1996, 39, 781-788). We have furth
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Autor:
Ball, Matthew, Boyd, Alistair, Churchill, Gwydion, Cuthbert, Murray, Drew, Mark, Fielding, Mark, Ford, Gair, Frodsham, Lianne, Golden, Michael, Leslie, Kevin, Lyons, Sarah, McKeever-Abbas, Ben, Stark, Andrew, Tomlin, Paula, Gottschling, Stephen, Hajar, Abraham, Jiang, Ji-long, Lo, Josephine, Suchozak, Bob
Publikováno v:
Organic Process Research & Development; May2012, Vol. 16 Issue 5, p741-747, 7p