| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
chemistry of opium alkaloids. part 44: Synthesis and opioid receptor binding profile of substituted ethenoisomorphinans and ethenomorphinans 1 Part XLIII. Baas, J. M. A.; Woudenberg, R. H.; Maat, L. Liebigs Ann./Recueil 1997, 13. 1
|
Maat, Leendert
|
|
1999
|
7 |
3 |
p. 529-541
13 p.
|
artikel
|
| 2 |
Discovery of non-peptidic P2–P3 butanediamide renin inhibitors with high oral efficacy
|
Simoneau, Bruno
|
|
1999
|
7 |
3 |
p. 489-508
20 p.
|
artikel
|
| 3 |
Dolichylpyrophosphate oligosaccharides: large-scale isolation and evaluation as oligosaccharyltransferase substrates
|
Gibbs, Barbara S
|
|
1999
|
7 |
3 |
p. 441-447
7 p.
|
artikel
|
| 4 |
Hybridized and isosteric analogues of N 1-acetyl-N 4-dimethyl-piperazinium iodide (ADMP) and N 1-phenyl-N 4-dimethyl-piperazinium iodide (DMPP) with central nicotinic action
|
Manetti, Dina
|
|
1999
|
7 |
3 |
p. 457-465
9 p.
|
artikel
|
| 5 |
N-2-(Azol-1(2)-yl)ethyliminodiacetic acids: a novel series of Gd(III) chelators as T2 relaxation agents for magnetic resonance imaging
|
López, Pilar
|
|
1999
|
7 |
3 |
p. 517-527
11 p.
|
artikel
|
| 6 |
2′,5′-Oligoadenylate-peptide nucleic acids (2–5A-PNAs) activate RNase L
|
Verheijen, Jeroen C
|
|
1999
|
7 |
3 |
p. 449-455
7 p.
|
artikel
|
| 7 |
Phosphodiesterase 4 inhibitors as airways smooth muscle relaxant agents: synthesis and biological activities of triazine derivatives
|
Leroux, F
|
|
1999
|
7 |
3 |
p. 509-516
8 p.
|
artikel
|
| 8 |
Synthesis and biological evaluation of novel 2′-deoxy-4′-thio-imidazole nucleosides
|
Wang, Y.
|
|
1999
|
7 |
3 |
p. 481-487
7 p.
|
artikel
|
| 9 |
Synthesis and evaluation of 2-amino-6-fluoro-9-(4-hydroxy-3-hydroxymethylbut-1-yl)purine mono- and diesters as potential prodrugs of penciclovir
|
Kim, Dae-Kee
|
|
1999
|
7 |
3 |
p. 565-570
6 p.
|
artikel
|
| 10 |
Synthesis of a fluorine-18 labeled derivative of epibatidine for in vivo nicotinic acetylcholine receptor PET imaging
|
Dolci, Lilian
|
|
1999
|
7 |
3 |
p. 467-479
13 p.
|
artikel
|
| 11 |
Synthesis of an antisense oligonucleotide targeted against C-raf kinase: efficient oligonucleotide synthesis without chlorinated solvents
|
Krotz, Achim H
|
|
1999
|
7 |
3 |
p. 435-439
5 p.
|
artikel
|
| 12 |
Synthesis of sialyl lewis x mimetics as selectin inhibitors by enzymatic aldol condensation reactions
|
Lin, Chun-Cheng
|
|
1999
|
7 |
3 |
p. 425-433
9 p.
|
artikel
|
| 13 |
The design, synthesis, and biological evaluation of analogues of the serine-threonine protein phosphatase 1 and 2A selective inhibitor microcystin LA: rational modifications imparting PP1 selectivity
|
Aggen, James B
|
|
1999
|
7 |
3 |
p. 543-564
22 p.
|
artikel
|
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