| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel and efficient synthesis of highly oxidized lignans by a methyltrioxorhenium/hydrogen peroxide catalytic system. Studies on their apoptogenic and antioxidant activity
|
Bernini, Roberta
|
|
2009
|
17 |
15 |
p. 5676-5682
7 p.
|
artikel
|
| 2 |
Anti-listerial activity and structure–activity relationships of the six major tyrocidines, cyclic decapeptides from Bacillus aneurinolyticus
|
Spathelf, Barbara M.
|
|
2009
|
17 |
15 |
p. 5541-5548
8 p.
|
artikel
|
| 3 |
Antimicrobial and immunomodulatory properties of prenylated xanthones from twigs of Garcinia staudtii
|
Ngoupayo, Joseph
|
|
2009
|
17 |
15 |
p. 5688-5695
8 p.
|
artikel
|
| 4 |
Antimicrobial natural products as β-ketoacyl-acyl carrier protein synthase III inhibitors
|
Lee, Jee-Young
|
|
2009
|
17 |
15 |
p. 5408-5413
6 p.
|
artikel
|
| 5 |
Design and synthesis of acetamido tri- and tetra-hydroxyazepanes: Potent and selective β-N-acetylhexosaminidase inhibitors
|
Li, Hongqing
|
|
2009
|
17 |
15 |
p. 5598-5604
7 p.
|
artikel
|
| 6 |
Design and synthesis of an all-in-one 3-(1,1-difluoroprop-2-ynyl)-3H-diazirin-3-yl functional group for photo-affinity labeling
|
Kumar, Nag S.
|
|
2009
|
17 |
15 |
p. 5388-5395
8 p.
|
artikel
|
| 7 |
Design and synthesis of new 1,3-benzthiazinan-4-one derivatives as selective cyclooxygenase (COX-2) inhibitors
|
Zarghi, Afshin
|
|
2009
|
17 |
15 |
p. 5369-5373
5 p.
|
artikel
|
| 8 |
Development of N-[11C]methylamino 4-hydroxy-2(1H)-quinolone derivatives as PET radioligands for the glycine-binding site of NMDA receptors
|
Fuchigami, Takeshi
|
|
2009
|
17 |
15 |
p. 5665-5675
11 p.
|
artikel
|
| 9 |
Discovery of novel dual functional agent as PPARγ agonist and 11β-HSD1 inhibitor for the treatment of diabetes
|
Ye, Yang-liang
|
|
2009
|
17 |
15 |
p. 5722-5732
11 p.
|
artikel
|
| 10 |
Discovery of novel thiourea derivatives as potent and selective β3-adrenergic receptor agonists
|
Maruyama, Tatsuya
|
|
2009
|
17 |
15 |
p. 5510-5519
10 p.
|
artikel
|
| 11 |
Discriminatory synergistic effect of Trp-substitutions in superagonist [(Arg/Lys)14, (Arg/Lys)15]nociceptin on ORL1 receptor binding and activation
|
Nishimura, Hirokazu
|
|
2009
|
17 |
15 |
p. 5683-5687
5 p.
|
artikel
|
| 12 |
Editorial board
|
|
|
2009
|
17 |
15 |
p. IFC-
1 p.
|
artikel
|
| 13 |
Effects of structural analogues of the substrate and allosteric regulator of the human mitochondrial NAD(P)+-dependent malic enzyme
|
Su, Kuo-Liang
|
|
2009
|
17 |
15 |
p. 5414-5419
6 p.
|
artikel
|
| 14 |
Glucose-based spiro-heterocycles as potent inhibitors of glycogen phosphorylase
|
Nagy, Veronika
|
|
2009
|
17 |
15 |
p. 5696-5707
12 p.
|
artikel
|
| 15 |
Graphical contents list
|
|
|
2009
|
17 |
15 |
p. 5357-5368
12 p.
|
artikel
|
| 16 |
Identification of potential cellular targets of aloisine A by affinity chromatography
|
Corbel, Caroline
|
|
2009
|
17 |
15 |
p. 5572-5582
11 p.
|
artikel
|
| 17 |
Identification, structure–activity relationships and molecular modeling of potent triamine and piperazine opioid ligands
|
Yongye, Austin B.
|
|
2009
|
17 |
15 |
p. 5583-5597
15 p.
|
artikel
|
| 18 |
Inhibitory effects of flavonoids isolated from Fragaria ananassa Duch on IgE-mediated degranulation in rat basophilic leukemia RBL-2H3
|
Itoh, Tomohiro
|
|
2009
|
17 |
15 |
p. 5374-5379
6 p.
|
artikel
|
| 19 |
Instructions to contributors
|
|
|
2009
|
17 |
15 |
p. I-
1 p.
|
artikel
|
| 20 |
Interaction of drug based binuclear mixed-ligand complexes with DNA
|
Patel, Mohan N.
|
|
2009
|
17 |
15 |
p. 5648-5655
8 p.
|
artikel
|
| 21 |
Muscarinic receptor 1 agonist activity of novel N-aryl carboxamide substituted 3-morpholino arecoline derivatives in Alzheimer’s presenile dementia models
|
Malviya, Manish
|
|
2009
|
17 |
15 |
p. 5526-5534
9 p.
|
artikel
|
| 22 |
NO-glibenclamide derivatives: Prototypes of a new class of nitric oxide-releasing anti-diabetic drugs
|
Calderone, Vincenzo
|
|
2009
|
17 |
15 |
p. 5426-5432
7 p.
|
artikel
|
| 23 |
‘Novel alkyl side chain sulfone 1α,25-dihydroxyvitamin D3 analogs: A comparison of in vitro antiproliferative activities and in vivo calcemic activities’
|
Usera, Aimee R.
|
|
2009
|
17 |
15 |
p. 5627-5631
5 p.
|
artikel
|
| 24 |
N-Terminal-prolonged vinyl ester-based peptides as selective proteasome β1 subunit inhibitors
|
Baldisserotto, Anna
|
|
2009
|
17 |
15 |
p. 5535-5540
6 p.
|
artikel
|
| 25 |
Parallel synthesis of potent dopaminergic N-phenyltriazole carboxamides applying a novel click chemistry based phenol linker
|
Loaiza, Pilar Rodriguez
|
|
2009
|
17 |
15 |
p. 5482-5487
6 p.
|
artikel
|
| 26 |
p-Guanidinoethyl calixarene and parent phenol derivatives exhibiting antibacterial activities. Synthesis and biological evaluation
|
Mourer, Maxime
|
|
2009
|
17 |
15 |
p. 5496-5509
14 p.
|
artikel
|
| 27 |
Polymer supported synthesis of aminooxyalkylated oligonucleotides, and some applications in the fabrication of microarrays
|
Sethi, D.
|
|
2009
|
17 |
15 |
p. 5442-5450
9 p.
|
artikel
|
| 28 |
Potent antitumor bifunctional DNA alkylating agents, synthesis and biological activities of 3a-aza-cyclopenta[a]indenes
|
Kakadiya, Rajesh
|
|
2009
|
17 |
15 |
p. 5614-5626
13 p.
|
artikel
|
| 29 |
Predictive models, based on classification algorithms, for compounds potentially active as mitochondrial ATP-sensitive potassium channel openers
|
Coi, Alessio
|
|
2009
|
17 |
15 |
p. 5565-5571
7 p.
|
artikel
|
| 30 |
Selective inhibition of nicotinamide adenine dinucleotide kinases by dinucleoside disulfide mimics of nicotinamide adenine dinucleotide analogues
|
Petrelli, Riccardo
|
|
2009
|
17 |
15 |
p. 5656-5664
9 p.
|
artikel
|
| 31 |
ssDNA aptamers that recognize diclofenac and 2-anilinophenylacetic acid
|
Joeng, Choon Bok
|
|
2009
|
17 |
15 |
p. 5380-5387
8 p.
|
artikel
|
| 32 |
7-((4-Substituted)piperazin-1-yl) derivatives of ciprofloxacin: Synthesis and in vitro biological evaluation as potential antitumor agents
|
Azéma, Joëlle
|
|
2009
|
17 |
15 |
p. 5396-5407
12 p.
|
artikel
|
| 33 |
Synergism of virtual screening and medicinal chemistry: Identification and optimization of allosteric antagonists of metabotropic glutamate receptor 1
|
Noeske, Tobias
|
|
2009
|
17 |
15 |
p. 5708-5715
8 p.
|
artikel
|
| 34 |
Syntheses and biological evaluations of carbosilane dendrimers uniformly functionalized with sialyl α(2→3) lactose moieties as inhibitors for human influenza viruses
|
Oka, Hiroyuki
|
|
2009
|
17 |
15 |
p. 5465-5475
11 p.
|
artikel
|
| 35 |
Synthesis and characterization of 6-deoxy-6-fluoro-d-fructose as a potential compound for imaging breast cancer with PET
|
Trayner, Brendan J.
|
|
2009
|
17 |
15 |
p. 5488-5495
8 p.
|
artikel
|
| 36 |
Synthesis and evaluation of a novel 2-azabicyclo[2.2.2]octane class of long chain fatty acid elongase 6 (ELOVL6) inhibitors
|
Sasaki, Takahide
|
|
2009
|
17 |
15 |
p. 5639-5647
9 p.
|
artikel
|
| 37 |
Synthesis and evaluation of a novel series of quinoline derivatives with immunosuppressive activity
|
Liu, Guo-Biao
|
|
2009
|
17 |
15 |
p. 5433-5441
9 p.
|
artikel
|
| 38 |
Synthesis, antimalarial activity and cytotoxicity of substituted 3,6-diphenyl-[1,2,4,5]tetraoxanes
|
Kumar, Nitin
|
|
2009
|
17 |
15 |
p. 5632-5638
7 p.
|
artikel
|
| 39 |
Synthesis, antiviral activity and molecular modeling of oxoquinoline derivatives
|
Santos, Fernanda da C.
|
|
2009
|
17 |
15 |
p. 5476-5481
6 p.
|
artikel
|
| 40 |
Synthesis, biological evaluation, and SAR study of novel pyrazole analogues as inhibitors of Mycobacterium tuberculosis: Part 2. Synthesis of rigid pyrazolones
|
Castagnolo, Daniele
|
|
2009
|
17 |
15 |
p. 5716-5721
6 p.
|
artikel
|
| 41 |
Synthesis, cannabinoid receptor affinity, molecular modeling studies and in vivo pharmacological evaluation of new substituted 1-aryl-5-(1H-pyrrol-1-yl)-1H-pyrazole-3-carboxamides. 2. Effect of the 3-carboxamide substituent on the affinity and selectivity profile
|
Silvestri, Romano
|
|
2009
|
17 |
15 |
p. 5549-5564
16 p.
|
artikel
|
| 42 |
Synthetic strategies toward carbocyclic purine–pyrimidine hybrid nucleosides
|
Sadler, Joshua M.
|
|
2009
|
17 |
15 |
p. 5520-5525
6 p.
|
artikel
|
| 43 |
Systematic syntheses of influenza neuraminidase inhibitors: A series of carbosilane dendrimers uniformly functionalized with thioglycoside-type sialic acid moieties
|
Sakamoto, Jun-Ichi
|
|
2009
|
17 |
15 |
p. 5451-5464
14 p.
|
artikel
|
| 44 |
UNA (unlocked nucleic acid): A flexible RNA mimic that allows engineering of nucleic acid duplex stability
|
Langkjær, Niels
|
|
2009
|
17 |
15 |
p. 5420-5425
6 p.
|
artikel
|
| 45 |
Urea and carbamate derivatives of primaquine: Synthesis, cytostatic and antioxidant activities
|
Šimunović, M.
|
|
2009
|
17 |
15 |
p. 5605-5613
9 p.
|
artikel
|
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