nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A credit-card library approach for disrupting protein–protein interactions
|
Xu, Yang |
|
2006 |
14 |
8 |
p. 2660-2673 14 p. |
artikel |
2 |
A modelling study of a non-concerted hydrolytic cycloaddition reaction by the catalytic antibody H11
|
Clark, Rachel L. |
|
2006 |
14 |
8 |
p. 2674-2683 10 p. |
artikel |
3 |
A novel naturally occurring tripyrrole with potential nuclease and anti-tumour properties
|
Subramanian, Mahesh |
|
2006 |
14 |
8 |
p. 2480-2486 7 p. |
artikel |
4 |
Antitumor agents 247. New 4-ethoxycarbonylethyl curcumin analogs as potential antiandrogenic agents
|
Lin, Li |
|
2006 |
14 |
8 |
p. 2527-2534 8 p. |
artikel |
5 |
Automated synthesis, characterization, and structural analysis of oligonucleotide C-3′-radical precursors
|
Lahoud, Georges |
|
2006 |
14 |
8 |
p. 2581-2588 8 p. |
artikel |
6 |
Binding free energy calculations of adenosine deaminase inhibitors
|
Coi, Alessio |
|
2006 |
14 |
8 |
p. 2636-2641 6 p. |
artikel |
7 |
Classification of dopamine, serotonin, and dual antagonists by decision trees
|
Kim, Hye-Jung |
|
2006 |
14 |
8 |
p. 2763-2770 8 p. |
artikel |
8 |
Design, synthesis, and biological evaluation of 1,3-diarylprop-2-en-1-ones : A novel class of cyclooxygenase-2 inhibitors
|
Zarghi, Afshin |
|
2006 |
14 |
8 |
p. 2600-2605 6 p. |
artikel |
9 |
Design, synthesis, and biological evaluation of substituted 3-alkylthio-4,5-diaryl-4H-1,2,4-triazoles as selective COX-2 inhibitors
|
Navidpour, Latifeh |
|
2006 |
14 |
8 |
p. 2507-2517 11 p. |
artikel |
10 |
Direct PCR amplification of various modified DNAs having amino acids: Convenient preparation of DNA libraries with high-potential activities for in vitro selection
|
Kuwahara, Masayasu |
|
2006 |
14 |
8 |
p. 2518-2526 9 p. |
artikel |
11 |
3D-QSAR and docking studies of aldehyde inhibitors of human cathepsin K
|
Pan, Xulin |
|
2006 |
14 |
8 |
p. 2771-2778 8 p. |
artikel |
12 |
Editorial Board
|
|
|
2006 |
14 |
8 |
p. CO2- 1 p. |
artikel |
13 |
Efficient approach to acyloxymethyl esters of nalidixic acid and in vitro evaluation as intra-ocular prodrugs
|
Azéma, Joëlle |
|
2006 |
14 |
8 |
p. 2569-2580 12 p. |
artikel |
14 |
Fluorescein-based amino acids for solid phase synthesis of fluorogenic protease substrates
|
Burchak, Olga N. |
|
2006 |
14 |
8 |
p. 2559-2568 10 p. |
artikel |
15 |
Furocoumarins from grapefruit juice and their effect on human CYP 3A4 and CYP 1B1 isoenzymes
|
Girennavar, Basavaraj |
|
2006 |
14 |
8 |
p. 2606-2612 7 p. |
artikel |
16 |
Graphical Contents List
|
|
|
2006 |
14 |
8 |
p. 2469-2479 11 p. |
artikel |
17 |
Instructions to contributors
|
|
|
2006 |
14 |
8 |
p. I- 1 p. |
artikel |
18 |
Natural products as starting materials for development of second-generation SERCA inhibitors targeted towards prostate cancer cells
|
Søhoel, Helmer |
|
2006 |
14 |
8 |
p. 2810-2815 6 p. |
artikel |
19 |
Neamine derivatives having a nucleobase with a lysine or an arginine as a linker, their synthesis and evaluation as potential inhibitors for HIV TAR–Tat
|
Yajima, Saki |
|
2006 |
14 |
8 |
p. 2799-2809 11 p. |
artikel |
20 |
New leads of metallo-β-lactamase inhibitors from structure-based pharmacophore design
|
Olsen, Lars |
|
2006 |
14 |
8 |
p. 2627-2635 9 p. |
artikel |
21 |
Novel cyano- and amidino-substituted derivatives of thieno[2,3-b]- and thieno[3,2-b]thiophene-2-carboxanilides and thieno[3′,2′:4,5]thieno- and thieno[2′,3′:4,5]thieno [2,3-c]quinolones: Synthesis, photochemical synthesis, DNA binding, and antitumor evaluation
|
Jarak, Ivana |
|
2006 |
14 |
8 |
p. 2859-2868 10 p. |
artikel |
22 |
α-Peptide/β-sulfonamidopeptide hybrids: Analogs of the chemotactic agent for-Met-Leu-Phe-OMe
|
Giordano, Cesare |
|
2006 |
14 |
8 |
p. 2642-2652 11 p. |
artikel |
23 |
QSAR models for Daphnia toxicity of pesticides based on combinations of topological parameters of molecular structures
|
Toropov, Andrey A. |
|
2006 |
14 |
8 |
p. 2779-2788 10 p. |
artikel |
24 |
Rapid and efficient oxidation of Hantzsch 1,4-dihydropyridines with sodium periodate catalyzed by manganese (III) Schiff base complexes
|
Nasr-Esfahani, Masoud |
|
2006 |
14 |
8 |
p. 2720-2724 5 p. |
artikel |
25 |
Sesquiterpene lactones as inhibitors of IL-8 expression in HeLa cells
|
Lindenmeyer, Maja T. |
|
2006 |
14 |
8 |
p. 2487-2497 11 p. |
artikel |
26 |
Synthesis and antifungal activity of substituted-10-methyl-1,2,3,4-tetrahydropyrazino[1,2-a]indoles
|
Tiwari, Rakesh Kumar |
|
2006 |
14 |
8 |
p. 2747-2752 6 p. |
artikel |
27 |
Synthesis and anti-inflammatory activity of a series of N-substituted naproxen glycolamides: Nitric oxide-donor naproxen prodrugs
|
Ranatunge, Ramani R. |
|
2006 |
14 |
8 |
p. 2589-2599 11 p. |
artikel |
28 |
Synthesis and appetite suppressant activity of 1-aryloxy-2-substituted aminomethyltetrahydronaphthalenes as conformationally rigid analogues of fluoxetine
|
Bhandari, Kalpana |
|
2006 |
14 |
8 |
p. 2535-2544 10 p. |
artikel |
29 |
Synthesis and binding affinities of methylvesamicol analogs for the acetylcholine transporter and sigma receptor
|
Shiba, Kazuhiro |
|
2006 |
14 |
8 |
p. 2620-2626 7 p. |
artikel |
30 |
Synthesis and biological evaluation of dimeric cinnamaldehydes as potent antitumor agents
|
Shin, Dae-Seop |
|
2006 |
14 |
8 |
p. 2498-2506 9 p. |
artikel |
31 |
Synthesis and CB1 receptor activities of dimethylheptyl derivatives of 2-arachidonoyl glycerol (2-AG) and 2-arachidonyl glyceryl ether (2-AGE)
|
Parkkari, Teija |
|
2006 |
14 |
8 |
p. 2850-2858 9 p. |
artikel |
32 |
Synthesis and cytotoxicity of new heterocyclic terpenylnaphthoquinones
|
Miguel del Corral, José M. |
|
2006 |
14 |
8 |
p. 2816-2827 12 p. |
artikel |
33 |
Synthesis and in vitro anti-hepatitis B virus activities of some ethyl 5-hydroxy-1H-indole-3-carboxylates
|
Zhao, Chunshen |
|
2006 |
14 |
8 |
p. 2552-2558 7 p. |
artikel |
34 |
Synthesis and in vitro evaluation of pseudosaccharinamine derivatives as potential elastase inhibitors
|
Rode, Haridas |
|
2006 |
14 |
8 |
p. 2789-2798 10 p. |
artikel |
35 |
Synthesis and pharmacology of pyrido[2,3-d]pyrimidinediones bearing polar substituents as adenosine receptor antagonists
|
Bulicz, Jacek |
|
2006 |
14 |
8 |
p. 2837-2849 13 p. |
artikel |
36 |
Synthesis and preliminary evaluation of new 1- and 3-[1-(2-hydroxy-3-phenoxypropyl)]xanthines from 2-amino-2-oxazolines as potential A1 and A2A adenosine receptor antagonists
|
Massip, Stéphane |
|
2006 |
14 |
8 |
p. 2697-2719 23 p. |
artikel |
37 |
Synthesis and study of the cancer cell growth inhibitory properties of α-, γ-tocopheryl and γ-tocotrienyl 2-phenylselenyl succinates
|
Vraka, Panayiota S. |
|
2006 |
14 |
8 |
p. 2684-2696 13 p. |
artikel |
38 |
Synthesis, antiproliferative and antifungal activities of some 2-(2,4-dihydroxyphenyl)-4H-3,1-benzothiazines
|
Matysiak, Joanna |
|
2006 |
14 |
8 |
p. 2613-2619 7 p. |
artikel |
39 |
Synthesis, biological evaluation, and pharmacokinetic study of prolyl-1-piperazinylacetic acid and prolyl-4-piperidinylacetic acid derivatives as VLA-4 antagonists
|
Chiba, Jun |
|
2006 |
14 |
8 |
p. 2725-2746 22 p. |
artikel |
40 |
Synthesis of 8-aminoadenosine 5′-(aminoalkyl phosphates), analogues of aminoacyl adenylates
|
Yousefi-Salakdeh, Esmail |
|
2006 |
14 |
8 |
p. 2653-2659 7 p. |
artikel |
41 |
Synthesis of new piperazine–pyridazinone derivatives and their binding affinity toward α1-, α2-adrenergic and 5-HT1A serotoninergic receptors
|
Betti, Laura |
|
2006 |
14 |
8 |
p. 2828-2836 9 p. |
artikel |
42 |
Synthesis of verbenachalcone congeners and their biological assessment against activation of the NGF-mediated neurite outgrowth of PC12D cells’ activity
|
Tanabe, Takamasa |
|
2006 |
14 |
8 |
p. 2753-2762 10 p. |
artikel |
43 |
Synthesis, stereochemical assignments, and biological activities of homoisoflavonoids
|
Siddaiah, Vidavalur |
|
2006 |
14 |
8 |
p. 2545-2551 7 p. |
artikel |