| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Alendronate
|
Shinkai, Ichiro
|
|
1996
|
4 |
1 |
p. 3-4
2 p.
|
artikel
|
| 2 |
Announcements
|
|
|
1996
|
4 |
1 |
p. v-vi
nvt p.
|
artikel
|
| 3 |
Contributors to this issue
|
|
|
1996
|
4 |
1 |
p. vii-
1 p.
|
artikel
|
| 4 |
Design, synthesis and in vitro evaluation of pyridinium ion based cyclase inhibitors and antifungal agents
|
Rose, Ingo C.
|
|
1996
|
4 |
1 |
p. 97-103
7 p.
|
artikel
|
| 5 |
Editorial
|
Wong, Chi-Huey
|
|
1996
|
4 |
1 |
p. iii-
1 p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
1996
|
4 |
1 |
p. IFC-
1 p.
|
artikel
|
| 7 |
Graphical abstracts
|
|
|
1996
|
4 |
1 |
p. ix-xii
nvt p.
|
artikel
|
| 8 |
Inhibition of aldose reductase by maesanin and related p-benzoquinone derivatives and effects on other enzymes
|
Haraguchi, Hiroyuki
|
|
1996
|
4 |
1 |
p. 49-53
5 p.
|
artikel
|
| 9 |
MS-271, a novel inhibitor of calmodulin-activated myosin light chain kinase from Streptomyces sp.—I. isolation, structural determination and biological properties of MS-271
|
Yano, Keiichi
|
|
1996
|
4 |
1 |
p. 115-120
6 p.
|
artikel
|
| 10 |
MS-271, A novel inhibitor of calmodulin-activated myosin light chain kinase from Streptomyces sp.—II. Solution structure of MS-271: Characteristic features of the ‘lasso’ structure
|
Katahira, Ritsuko
|
|
1996
|
4 |
1 |
p. 121-129
9 p.
|
artikel
|
| 11 |
N-Cubylmethyl substituted morphinoids as novel narcotic antagonists
|
Cheng, Chen-Yu
|
|
1996
|
4 |
1 |
p. 73-80
8 p.
|
artikel
|
| 12 |
Novel designed enediynes: Molecular design, chemical synthesis, mode of cycloaromatization and guanine-specific DNA cleavage
|
Toshima, Kazunobu
|
|
1996
|
4 |
1 |
p. 105-113
9 p.
|
artikel
|
| 13 |
Overexpression, one-step purification and characterization of UDP-glucose dehydrogenase and UDP-N-acetylglucosamine pyrophosphorylase
|
De Luca, Claudio
|
|
1996
|
4 |
1 |
p. 131-141
11 p.
|
artikel
|
| 14 |
Peptide Nucleic Acids (PNA): Synthesis, properties and potential applications
|
Hyrup, Birgitte
|
|
1996
|
4 |
1 |
p. 5-23
19 p.
|
artikel
|
| 15 |
Synthesis and activity of 1-N-iminosugar inhibitors, siastatin B analogues for α-N-acetylgalactosaminidase and β-N-acetylglucosaminidase
|
Nishimura, Yoshio
|
|
1996
|
4 |
1 |
p. 91-96
6 p.
|
artikel
|
| 16 |
Synthesis and in vitro antibacterial activity of spermidine-based mixed catechol- and hydroxamate-containing siderophore—Vancomycin conjugates
|
Ghosh, Manuka
|
|
1996
|
4 |
1 |
p. 43-48
6 p.
|
artikel
|
| 17 |
Synthesis of hexahydrocyclopentimidazol-2-(1H)-one derivatives displaying selective DP-receptor agonist properties
|
Barraclough, Paul
|
|
1996
|
4 |
1 |
p. 81-90
10 p.
|
artikel
|
| 18 |
The absolute configuration of adjacent bis-THF acetogenins and asiminocin, a novel highly potent asimicin isomer from Asimina triloba
|
Zhao, Geng-Xian
|
|
1996
|
4 |
1 |
p. 25-32
8 p.
|
artikel
|
| 19 |
The design of dipeptide helical mimetics: The synthesis, tachykinin receptor affinity and conformational analysis of 1,1,6-trisubstituted indanes
|
Horwell, David C.
|
|
1996
|
4 |
1 |
p. 33-42
10 p.
|
artikel
|
| 20 |
Using SAR and QSAR analysis to model the activity and structure of the quinolone—DNA complex
|
Llorente, Belsis
|
|
1996
|
4 |
1 |
p. 61-71
11 p.
|
artikel
|
| 21 |
Valacyclovir
|
Shinkai, Ichiro
|
|
1996
|
4 |
1 |
p. 1-2
2 p.
|
artikel
|
| 22 |
Vinyl fluoride as a mimic of the ‘intermediate’ enol form in the 5α-reductase transformation: Synthesis and in vitro activity of (N-1′,1′-Dimethylethyl)-3-haloandrost-3,5-diene-17β-carboxamides
|
Li, Xun
|
|
1996
|
4 |
1 |
p. 55-60
6 p.
|
artikel
|
Tijdschrift beschrijving