Zobrazeno 1 - 10
of 60
pro vyhledávání: '"E Binderup"'
Autor:
A S, Weiskopf, P, Vouros, J, Cunniff, E, Binderup, F, Björkling, L, Binderup, M C, White, G H, Posner
Publikováno v:
Journal of mass spectrometry : JMS. 36(1)
The structural specificity of vitamin D derivatization by PTAD (4-phenyl-1,2,4-triazoline-3,5-dione) was probed using synthetic analogues and ion trap mass spectrometry. EB 1089, a vitamin D(3) analogue which contains a second site for Diels--Alder c
Publikováno v:
Current pharmaceutical design. 6(7)
It is well established that the metabolically active form of vitamin D, 1alpha,25-dihydroxyvitamin D 3 (1alpha,25(OH)2 D 3 ) plays a key role in the establishment and maintenance of the calcium metabolism in the body. In addition to this classic effe
Publikováno v:
British journal of pharmacology. 125(4)
1. 1alpha,25-dihydroxyvitamin3 (VD) is a nuclear hormone that has important cell regulatory functions but also a strong calcemic effect. EB1089 is a potent antiproliferative VD analogue, which has a modified side chain resulting in increased metaboli
Autor:
Graham R. Williams, E. Binderup, Glenville Jones, M. J. Calverley, A.-M. Kissmeyer, F. J. Dilworth, J. L. Nielsen, Hugh L.J. Makin
Publikováno v:
Scopus-Elsevier
Vitamin D analogs are valuable drugs with established and potential uses in hyperproliferative disorders. Lexacalcitol (KH1060) is over 100 times more active than 1alpha,25-dihydroxyvitamin D3 [1alpha,25-(OH)2D3], as judged by in vitro antiproliferat
Publikováno v:
Vitamin D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::931dd6cc7fd48a2192cfac7e9d06d50b
https://doi.org/10.1515/9783110882513-025
https://doi.org/10.1515/9783110882513-025
Autor:
A.-M. Kissmeyer, E. Binderup, Glenville Jones, V.N. Shankar, D.J.H. Trafford, N.J. Schroeder, H.L.J. Makin, Martin John Calverley
Publikováno v:
Bone. 17:326
Autor:
E. Binderup
Publikováno v:
Drugs of the Future. 15:15
Autor:
W. O. Godtfredsen, B. Baltzer, H. Sorensen, W. von Daehne, E. Binderup, B. Nielsen, S. Vangedal, K. Hansen
Publikováno v:
The Journal of Antibiotics. 33:1183-1192
The principle of combining a beta-lactam antibiotic with a beta-lactamase inhibitor in a single molecule functioning as pro-drug for the two active components is illustrated by the linked esters 3 and 4 in which ampicillin and mecillinam, respectivel
Autor:
E. Binderup, E. T. Hansen
Publikováno v:
Synthetic Communications. 14:857-864
During a search for a satisfactory synthesis of chloromethyl esters 1 of certain β-lactam antibiotics, e.g. penicillanic acid sulfone, we discovered that chloromethyl chlorosulfate1 (4) is an excellent reagent for this purpose. We also found that ot
Publikováno v:
Acta Chemica Scandinavica. 21:1984-1986