| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A combined NMR and molecular dynamics simulation study to determine the conformational properties of agonists and antagonists against experimental autoimmune encephalomyelitis
|
Mantzourani, Efthimia D.
|
|
2008
|
16 |
5 |
p. 2171-2182
12 p.
|
artikel
|
| 2 |
Activation and inhibition of DNA methyltransferases by S-adenosyl-l-homocysteine analogues
|
Kumar, Ritesh
|
|
2008
|
16 |
5 |
p. 2276-2285
10 p.
|
artikel
|
| 3 |
Activity of Mannich bases of 7-hydroxycoumarin against Flaviviridae
|
Mazzei, Mauro
|
|
2008
|
16 |
5 |
p. 2591-2605
15 p.
|
artikel
|
| 4 |
Alachalasins A–G, new cytochalasins from the fungus Stachybotrys charatum
|
Zhang, Yonggang
|
|
2008
|
16 |
5 |
p. 2627-2634
8 p.
|
artikel
|
| 5 |
Amphiphilic chitosan nanosphere: Studies on formation, toxicity, and guest molecule incorporation
|
Yoksan, Rangrong
|
|
2008
|
16 |
5 |
p. 2687-2696
10 p.
|
artikel
|
| 6 |
α- and β-Substituted phosphonate analogs of LPA as autotaxin inhibitors
|
Cui, Peng
|
|
2008
|
16 |
5 |
p. 2212-2225
14 p.
|
artikel
|
| 7 |
Bornyl (3,4,5-trihydroxy)-cinnamate - An optimized human neutrophil elastase inhibitor designed by free energy calculations
|
Steinbrecher, Thomas
|
|
2008
|
16 |
5 |
p. 2385-2390
6 p.
|
artikel
|
| 8 |
Designed modification of partial agonist of ORL1 nociceptin receptor for conversion into highly potent antagonist
|
Li, Jinglan
|
|
2008
|
16 |
5 |
p. 2635-2644
10 p.
|
artikel
|
| 9 |
1,3-Dipropyl-8-(1-phenylacetamide-1H-pyrazol-3-yl)-xanthine derivatives as highly potent and selective human A2B adenosine receptor antagonists
|
Tabrizi, Mojgan Aghazadeh
|
|
2008
|
16 |
5 |
p. 2419-2430
12 p.
|
artikel
|
| 10 |
Discovery of sulfonylalkylamides: A new class of orally active factor Xa inhibitors
|
Imaeda, Yasuhiro
|
|
2008
|
16 |
5 |
p. 2243-2260
18 p.
|
artikel
|
| 11 |
Docking and hydropathic scoring of polysubstituted pyrrole compounds with antitubulin activity
|
Tripathi, Ashutosh
|
|
2008
|
16 |
5 |
p. 2235-2242
8 p.
|
artikel
|
| 12 |
Editorial board
|
|
|
2008
|
16 |
5 |
p. IFC-
1 p.
|
artikel
|
| 13 |
Fluorinated methylenecyclopropane analogues of nucleosides. Synthesis and antiviral activity of (Z)- and (E)-9-{[(2-fluoromethyl-2-hydroxymethyl)-cyclopropylidene]methyl}adenine and -guanine
|
Li, Chengwei
|
|
2008
|
16 |
5 |
p. 2148-2155
8 p.
|
artikel
|
| 14 |
Functional assay and structure–activity relationships of new third-generation P-glycoprotein inhibitors
|
Müller, Henrik
|
|
2008
|
16 |
5 |
p. 2448-2462
15 p.
|
artikel
|
| 15 |
Fused bicyclic pyrrolizinones as new scaffolds for human NK1 antagonists
|
Morriello, Gregori J.
|
|
2008
|
16 |
5 |
p. 2156-2170
15 p.
|
artikel
|
| 16 |
Glyconanobiotics: Novel carbohydrated nanoparticle antibiotics for MRSA and Bacillus anthracis
|
Abeylath, Sampath C.
|
|
2008
|
16 |
5 |
p. 2412-2418
7 p.
|
artikel
|
| 17 |
Graphical contents list
|
|
|
2008
|
16 |
5 |
p. 2135-2147
13 p.
|
artikel
|
| 18 |
Imidazolidines as new anti-Trypanosoma cruzi agents: Biological evaluation and structure–activity relationships
|
Caterina, M. Cristina
|
|
2008
|
16 |
5 |
p. 2226-2234
9 p.
|
artikel
|
| 19 |
Improved syntheses and applicability of different DOTA building blocks for multiply derivatized scaffolds
|
Wängler, C.
|
|
2008
|
16 |
5 |
p. 2606-2616
11 p.
|
artikel
|
| 20 |
Instructions to contributors
|
|
|
2008
|
16 |
5 |
p. I-
1 p.
|
artikel
|
| 21 |
Low molecular weight lignin suppresses activation of NF-κB and HIV-1 promoter
|
Mitsuhashi, Shinya
|
|
2008
|
16 |
5 |
p. 2645-2650
6 p.
|
artikel
|
| 22 |
Molecular modeling study and synthesis of novel pyrrolo[2,3-d]pyrimidines and pyrrolotriazolopyrimidines of expected antitumor and radioprotective activities
|
Abou El Ella, Dalal A.
|
|
2008
|
16 |
5 |
p. 2391-2402
12 p.
|
artikel
|
| 23 |
ω-(2-Naphthyloxy) amino alkanes as a novel class of anti-hyperglycemic and lipid lowering agents
|
Chaturvedi, Devdutt
|
|
2008
|
16 |
5 |
p. 2489-2498
10 p.
|
artikel
|
| 24 |
N δ-Methylated l-arginine derivatives and their effects on the nitric oxide generating system
|
Kotthaus, Jürke
|
|
2008
|
16 |
5 |
p. 2305-2312
8 p.
|
artikel
|
| 25 |
Novel AMPA and kainate receptor antagonists containing the pyrazolo[1,5-c]quinazoline ring system: Synthesis and structure–activity relationships
|
Varano, Flavia
|
|
2008
|
16 |
5 |
p. 2617-2626
10 p.
|
artikel
|
| 26 |
Novel 2-(4-methylsulfonylphenyl)pyrimidine derivatives as highly potent and specific COX-2 inhibitors
|
Orjales, Aurelio
|
|
2008
|
16 |
5 |
p. 2183-2199
17 p.
|
artikel
|
| 27 |
Novel quinazolinone derivatives as 5-HT7 receptor ligands
|
Na, Yong Ho
|
|
2008
|
16 |
5 |
p. 2570-2578
9 p.
|
artikel
|
| 28 |
Parallel synthesis of a series of potentially brain penetrant aminoalkyl benzoimidazoles
|
Micco, Iolanda
|
|
2008
|
16 |
5 |
p. 2313-2328
16 p.
|
artikel
|
| 29 |
Rate enhancement of the oxidative folding of lysozyme by the use of aromatic thiol containing redox buffers
|
Gurbhele-Tupkar, Minakshi C.
|
|
2008
|
16 |
5 |
p. 2579-2590
12 p.
|
artikel
|
| 30 |
Requirement of β-alanine components in sequence-specific DNA alkylation by pyrrole–imidazole conjugates with seven-base pair recognition
|
Bando, Toshikazu
|
|
2008
|
16 |
5 |
p. 2286-2291
6 p.
|
artikel
|
| 31 |
SAR studies of capsazepinoid bronchodilators. Part 2: Chlorination and catechol replacement in the A-ring
|
Berglund, Magnus
|
|
2008
|
16 |
5 |
p. 2513-2528
16 p.
|
artikel
|
| 32 |
SAR studies of capsazepinoid bronchodilators. Part 1: The importance of the catechol moiety and aspects of the B-ring structure
|
Dalence-Guzmán, Marı´a F.
|
|
2008
|
16 |
5 |
p. 2499-2512
14 p.
|
artikel
|
| 33 |
SAR studies of capsazepinoid bronchodilators 3: The thiourea part (coupling region) and the 2-(4-chlorophenyl)ethyl moiety (C-region)
|
Berglund, Magnus
|
|
2008
|
16 |
5 |
p. 2529-2540
12 p.
|
artikel
|
| 34 |
Selective COX-2 inhibitors. Part 2: Synthesis and biological evaluation of 4-benzylideneamino- and 4-phenyliminomethyl-benzenesulfonamides
|
Lin, Shwu-Jiuan
|
|
2008
|
16 |
5 |
p. 2697-2706
10 p.
|
artikel
|
| 35 |
Stereospecific synthesis and bio-activity of novel β3-adrenoceptor agonists and inverse agonists
|
Perrone, Maria Grazia
|
|
2008
|
16 |
5 |
p. 2473-2488
16 p.
|
artikel
|
| 36 |
Structural insights into hydroxycoumarin-induced apoptosis in U-937 cells
|
Riveiro, Maria E.
|
|
2008
|
16 |
5 |
p. 2665-2675
11 p.
|
artikel
|
| 37 |
Structural requirements for the stability of novel cephalosporins to AmpC β-lactamase based on 3D-structure
|
Murano, Kenji
|
|
2008
|
16 |
5 |
p. 2261-2275
15 p.
|
artikel
|
| 38 |
Structure–activity relationships in the inhibition of monoamine oxidase B by 1-methyl-3-phenylpyrroles
|
Ogunrombi, Modupe O.
|
|
2008
|
16 |
5 |
p. 2463-2472
10 p.
|
artikel
|
| 39 |
Structure–activity study of 2,3-benzodiazepin-4-ones noncompetitive AMPAR antagonists: Identification of the 1-(4-amino-3-methylphenyl)-3,5-dihydro-7,8-ethylenedioxy-4H-2,3-benzodiazepin-4-one as neuroprotective agent
|
Micale, Nicola
|
|
2008
|
16 |
5 |
p. 2200-2211
12 p.
|
artikel
|
| 40 |
Synthesis and anticonvulsant evaluation of N-substituted isoquinoline AMPA receptor antagonists
|
Gitto, Rosaria
|
|
2008
|
16 |
5 |
p. 2379-2384
6 p.
|
artikel
|
| 41 |
Synthesis and antimycobacterial evaluation of newer 1-cyclopropyl-1,4-dihydro-6-fluoro-7-(substituted secondary amino)-8-methoxy-5-(sub)-4-oxoquinoline-3-carboxylic acids
|
Senthilkumar, Palaniappan
|
|
2008
|
16 |
5 |
p. 2558-2569
12 p.
|
artikel
|
| 42 |
Synthesis and antiproliferative activity of benzyl and phenethyl analogs of makaluvamines
|
Shinkre, Bidhan A.
|
|
2008
|
16 |
5 |
p. 2541-2549
9 p.
|
artikel
|
| 43 |
Synthesis and biological evaluation of imidazol-2-one derivatives as potential antitumor agents
|
Xue, Na
|
|
2008
|
16 |
5 |
p. 2550-2557
8 p.
|
artikel
|
| 44 |
Synthesis and biological evaluation of pyrroloiminoquinone derivatives
|
Passarella, Daniele
|
|
2008
|
16 |
5 |
p. 2431-2438
8 p.
|
artikel
|
| 45 |
Synthesis and evaluation of antitumoral activity of ester and amide derivatives of 2-arylamino-6-trifluoromethyl-3-pyridinecarboxylic acids
|
Onnis, Valentina
|
|
2008
|
16 |
5 |
p. 2367-2378
12 p.
|
artikel
|
| 46 |
Synthesis and solution conformation studies of 3-substituted uridine and pseudouridine derivatives
|
Chang, Yu-Cheng
|
|
2008
|
16 |
5 |
p. 2676-2686
11 p.
|
artikel
|
| 47 |
Synthesis and structure–immunosuppressive activity relationships of bakuchiol and its derivatives
|
Chen, Hongli
|
|
2008
|
16 |
5 |
p. 2403-2411
9 p.
|
artikel
|
| 48 |
Synthesis, cytostatic and anti-HCV activity of 6-(N-substituted aminomethyl)-, 6-(O-substituted hydroxymethyl)- and 6-(S-substituted sulfanylmethyl)purine nucleosides
|
Šilhár, Peter
|
|
2008
|
16 |
5 |
p. 2329-2366
38 p.
|
artikel
|
| 49 |
Synthesis, nitric oxide release, and anti-leukemic activity of glutathione-activated nitric oxide prodrugs: Structural analogues of PABA/NO, an anti-cancer lead compound
|
Chakrapani, Harinath
|
|
2008
|
16 |
5 |
p. 2657-2664
8 p.
|
artikel
|
| 50 |
Synthesis of novel oxazolidinone antimicrobial agents
|
Ebner, David C.
|
|
2008
|
16 |
5 |
p. 2651-2656
6 p.
|
artikel
|
| 51 |
The number and distances of positive charges of polyamine side chains in a series of perylene diimides significantly influence their ability to induce G-quadruplex structures and inhibit human telomerase
|
Franceschin, Marco
|
|
2008
|
16 |
5 |
p. 2292-2304
13 p.
|
artikel
|
| 52 |
Three-dimensional quantitative structure–activity relationship studies on novel series of benzotriazine based compounds acting as Src inhibitors using CoMFA and CoMSIA
|
Gueto, Carlos
|
|
2008
|
16 |
5 |
p. 2439-2447
9 p.
|
artikel
|
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