| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A DFT-based QSARs study of protoporphyrinogen oxidase inhibitors: phenyl triazolinones
|
Zhang, Li
|
|
2004
|
12 |
23 |
p. 6183-6191
9 p.
|
artikel
|
| 2 |
A novel class of achiral seco-analogs of CC-1065 and the duocarmycins: design, synthesis, DNA binding, and anticancer properties
|
Kupchinsky, Stanley
|
|
2004
|
12 |
23 |
p. 6221-6236
16 p.
|
artikel
|
| 3 |
Bisquaternary caracurine V and iso-caracurine V salts as ligands for the muscle type of nicotinic acetylcholine receptors: SAR and QSAR studies
|
Zlotos, D.P.
|
|
2004
|
12 |
23 |
p. 6277-6285
9 p.
|
artikel
|
| 4 |
Carboxylic acid and phosphate ester derivatives of fluconazole: synthesis and antifungal activities
|
Nam, Nguyen-Hai
|
|
2004
|
12 |
23 |
p. 6255-6269
15 p.
|
artikel
|
| 5 |
Chrysin and its phosphate ester inhibit cell proliferation and induce apoptosis in Hela cells
|
Zhang, Ting
|
|
2004
|
12 |
23 |
p. 6097-6105
9 p.
|
artikel
|
| 6 |
Contributors to this issue
|
|
|
2004
|
12 |
23 |
p. I-
1 p.
|
artikel
|
| 7 |
Corrigendum to “Design and synthesis of Rho kinase inhibitors (I)”
|
Takami, Atsuya
|
|
2004
|
12 |
23 |
p. 6317-
1 p.
|
artikel
|
| 8 |
Editorial board
|
|
|
2004
|
12 |
23 |
p. IFC-
1 p.
|
artikel
|
| 9 |
Flexible docking of pyridinone derivatives into the non-nucleoside inhibitor binding site of HIV-1 reverse transcriptase
|
Medina-Franco, José Luis
|
|
2004
|
12 |
23 |
p. 6085-6095
11 p.
|
artikel
|
| 10 |
Fluorescent ε-ATP analogues for probing physicochemical properties of proteins. Synthesis, biochemical evaluation, and sensitivity to properties of the medium
|
Sharon, Einat
|
|
2004
|
12 |
23 |
p. 6119-6135
17 p.
|
artikel
|
| 11 |
Graphical contents list
|
|
|
2004
|
12 |
23 |
p. 6021-6027
7 p.
|
artikel
|
| 12 |
Inhibition of human β-tryptase by Bowman–Birk inhibitor derived peptides: creation of a new tri-functional inhibitor
|
Scarpi, Dina
|
|
2004
|
12 |
23 |
p. 6045-6052
8 p.
|
artikel
|
| 13 |
Instructions to contributors
|
|
|
2004
|
12 |
23 |
p. III-VII
nvt p.
|
artikel
|
| 14 |
Ionization, lipophilicity, and molecular modeling to investigate permeability and other biological properties of amlodipine
|
Caron, Giulia
|
|
2004
|
12 |
23 |
p. 6107-6118
12 p.
|
artikel
|
| 15 |
Literature
|
|
|
2004
|
12 |
23 |
p. 6319-6320
2 p.
|
artikel
|
| 16 |
Molecular docking and 3D QSAR studies on 1-amino-2-phenyl-4-(piperidin-1-yl)-butanes based on the structural modeling of human CCR5 receptor
|
Xu, Yong
|
|
2004
|
12 |
23 |
p. 6193-6208
16 p.
|
artikel
|
| 17 |
New lupane triterpenoids from Solidago canadensis that inhibit the lyase activity of DNA polymerase β
|
Chaturvedula, V.S. Prakash
|
|
2004
|
12 |
23 |
p. 6271-6275
5 p.
|
artikel
|
| 18 |
Preparation and preliminary biological evaluation of a 177Lu labeled sanazole derivative for possible use in targeting tumor hypoxia
|
Das, Tapas
|
|
2004
|
12 |
23 |
p. 6077-6084
8 p.
|
artikel
|
| 19 |
Pyrazole derivatives as new potent and selective 20-hydroxy-5,8,11,14-eicosatetraenoic acid synthase inhibitors
|
Nakamura, Toshio
|
|
2004
|
12 |
23 |
p. 6209-6219
11 p.
|
artikel
|
| 20 |
Quantitative structure–activity relationship study using refractotopological state atom index on some neonicotinoid insecticides
|
Debnath, Bikash
|
|
2004
|
12 |
23 |
p. 6137-6145
9 p.
|
artikel
|
| 21 |
Serendipitous discovery of an unexpected rearrangement leads to two new classes of potential protease inhibitors
|
Zhong, Jiaying
|
|
2004
|
12 |
23 |
p. 6249-6254
6 p.
|
artikel
|
| 22 |
Solution chemistry and cytotoxic properties of novel organogold(III) compounds
|
Messori, Luigi
|
|
2004
|
12 |
23 |
p. 6039-6043
5 p.
|
artikel
|
| 23 |
Sphingolipids as coenzymes in anion transfer and tumor death
|
Radin, Norman S.
|
|
2004
|
12 |
23 |
p. 6029-6037
9 p.
|
artikel
|
| 24 |
Structural requirements for 2,4- and 3,6-disubstituted pyran biomimetics of cis-(6-benzhydryl-piperidin-3-yl)-benzylamine compounds to interact with monoamine transporters
|
Zhang, Shijun
|
|
2004
|
12 |
23 |
p. 6301-6315
15 p.
|
artikel
|
| 25 |
Studies of nonnucleoside HIV-1 reverse transcriptase inhibitors. Part 1: Design and synthesis of thiazolidenebenzenesulfonamides
|
Masuda, Naoyuki
|
|
2004
|
12 |
23 |
p. 6171-6182
12 p.
|
artikel
|
| 26 |
Syntheses and bioactivities of macrocyclic paclitaxel bis-lactones
|
Liu, Changhui
|
|
2004
|
12 |
23 |
p. 6147-6161
15 p.
|
artikel
|
| 27 |
Synthesis and biological evaluation of 5R- and 5S-methyl substituted d- and l-configuration 1,3-dioxolane nucleoside analogs
|
Bera, Sanjib
|
|
2004
|
12 |
23 |
p. 6237-6247
11 p.
|
artikel
|
| 28 |
Synthesis and structure–activity correlations of the cytotoxic bifunctional 1,4-diamidoanthraquinone derivatives
|
Huang, Hsu-Shan
|
|
2004
|
12 |
23 |
p. 6163-6170
8 p.
|
artikel
|
| 29 |
Synthesis and structure–activity relationships of potent 3- or 4-substituted-2-cyanopyrrolidine dipeptidyl peptidase IV inhibitors
|
Fukushima, Hiroshi
|
|
2004
|
12 |
23 |
p. 6053-6061
9 p.
|
artikel
|
| 30 |
Synthesis and topoisomerase I inhibitory properties of luotonin A analogues
|
Cagir, Ali
|
|
2004
|
12 |
23 |
p. 6287-6299
13 p.
|
artikel
|
| 31 |
The synthesis of phosphorylated disaccharide components of the extracellular phosphomannan of Pichia (Hansenula) holstii NRRL Y-2448
|
Fairweather, Jon K.
|
|
2004
|
12 |
23 |
p. 6063-6075
13 p.
|
artikel
|
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