nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A chromone analog inhibits TNF-α induced expression of cell adhesion molecules on human endothelial cells via blocking NF-κB activation
|
Kumar, Sarvesh |
|
2007 |
15 |
8 |
p. 2952-2962 11 p. |
artikel |
2 |
A conformational transition in the adenylyl cyclase catalytic site yields different binding modes for ribosyl-modified and unmodified nucleotide inhibitors
|
Wang, Jenna L. |
|
2007 |
15 |
8 |
p. 2993-3002 10 p. |
artikel |
3 |
Acridone derivatives: Design, synthesis, and inhibition of breast cancer resistance protein ABCG2
|
Boumendjel, Ahcene |
|
2007 |
15 |
8 |
p. 2892-2897 6 p. |
artikel |
4 |
5-Alkynyl-2′-deoxyuridines: Chromatography-free synthesis and cytotoxicity evaluation against human breast cancer cells
|
Meneni, Srinivasarao |
|
2007 |
15 |
8 |
p. 3082-3088 7 p. |
artikel |
5 |
Antimalarial activity of 1-aryl-3,3-dialkyltriazenes
|
Nishiwaki, Keiji |
|
2007 |
15 |
8 |
p. 2856-2859 4 p. |
artikel |
6 |
1-(5-Carboxy- and 5-carbamoylindol-1-yl)propan-2-ones as inhibitors of human cytosolic phospholipase A2α: Bioisosteric replacement of the carboxylic acid and carboxamide moiety
|
Hess, Mark |
|
2007 |
15 |
8 |
p. 2883-2891 9 p. |
artikel |
7 |
Chemical synthesis and biological activities of 16α-derivatives of 5α-androstane-3α,17β-diol as antiandrogens
|
Roy, Jenny |
|
2007 |
15 |
8 |
p. 3003-3018 16 p. |
artikel |
8 |
Clavaminols A–F, novel cytotoxic 2-amino-3-alkanols from the ascidian Clavelina phlegraea
|
Aiello, Anna |
|
2007 |
15 |
8 |
p. 2920-2926 7 p. |
artikel |
9 |
Computational approach to the basicity of a series of α1-adrenoceptor ligands in aqueous solution
|
Kinsella, Gemma K. |
|
2007 |
15 |
8 |
p. 2850-2855 6 p. |
artikel |
10 |
Computational neural network analysis of the affinity of lobeline and tetrabenazine analogs for the vesicular monoamine transporter-2
|
Zheng, Fang |
|
2007 |
15 |
8 |
p. 2975-2992 18 p. |
artikel |
11 |
Cyathane diterpenes from Sarcodon cyrneus and evaluation of their activities of neuritegenesis and nerve growth factor production
|
Marcotullio, Maria Carla |
|
2007 |
15 |
8 |
p. 2878-2882 5 p. |
artikel |
12 |
Cytochrome P-450 model reactions: Efficient and highly selective oxidation of alcohols with tetrabutylammonium peroxymonosulfate catalyzed by Mn-porphyrins
|
Rezaeifard, Abdolreza |
|
2007 |
15 |
8 |
p. 3097-3101 5 p. |
artikel |
13 |
Editorial board
|
|
|
2007 |
15 |
8 |
p. IFC- 1 p. |
artikel |
14 |
Free radical trapping properties of several ethyl-substituted derivatives of 5-ethoxycarbonyl-5-methyl-1-pyrroline N-oxide (EMPO)
|
Stolze, Klaus |
|
2007 |
15 |
8 |
p. 2827-2836 10 p. |
artikel |
15 |
Graphical contents list
|
|
|
2007 |
15 |
8 |
p. 2801-2809 9 p. |
artikel |
16 |
Hybrid molecules of estrone: New compounds with potential antibacterial, antifungal, and antiproliferative activities
|
Adamec, J. |
|
2007 |
15 |
8 |
p. 2898-2906 9 p. |
artikel |
17 |
Identification of antitumour activity of novel derivatives of 8-aryl-2,6,7,8-tetrahydroimidazo[2,1-c][1,2,4]triazine-3,4-dione and 8-aryl-4-imino-2,3,7,8-tetrahydroimidazo[2,1-c][1,2,4]triazin-3(6H)-one
|
Sztanke, Krzysztof |
|
2007 |
15 |
8 |
p. 2837-2849 13 p. |
artikel |
18 |
Instructions to contributors
|
|
|
2007 |
15 |
8 |
p. I- 1 p. |
artikel |
19 |
Modeling of human ghrelin receptor (hGHS-R1a) in its close state and validation by molecular docking
|
Pedretti, Alessandro |
|
2007 |
15 |
8 |
p. 3054-3064 11 p. |
artikel |
20 |
Novel class of arylpiperazines containing N-acylated amino acids: Their synthesis, 5-HT1A, 5-HT2A receptor affinity, and in vivo pharmacological evaluation
|
Zajdel, Paweł |
|
2007 |
15 |
8 |
p. 2907-2919 13 p. |
artikel |
21 |
Novel 1-oxyl-2-substitutedphenyl-4,4,5,5-tetramethylimidazolines: Synthesis, selectively analgesic action, and QSAR analysis
|
Zhao, Ming |
|
2007 |
15 |
8 |
p. 2815-2826 12 p. |
artikel |
22 |
Novel selective human mitochondrial kinase inhibitors: Design, synthesis and enzymatic activity
|
Ciliberti, Nunzia |
|
2007 |
15 |
8 |
p. 3065-3081 17 p. |
artikel |
23 |
Quantitative structure–activity relationship of sesquiterpene lactones with cytotoxic activity
|
Scotti, Marcus T. |
|
2007 |
15 |
8 |
p. 2927-2934 8 p. |
artikel |
24 |
Short-chain 3-ketoceramides, strong apoptosis inducers against human leukemia HL-60 cells
|
Azuma, Hideki |
|
2007 |
15 |
8 |
p. 2860-2867 8 p. |
artikel |
25 |
Structure–activity based study of the Smac-binding pocket within the BIR3 domain of XIAP
|
Wist, Aislyn D. |
|
2007 |
15 |
8 |
p. 2935-2943 9 p. |
artikel |
26 |
Substitution at the 8-position of 3″-deoxy-cyclic ADP-carbocyclic-ribose, a highly potent Ca2+-mobilizing agent, provides partial agonists 1
|
Kudoh, Takashi |
|
2007 |
15 |
8 |
p. 3032-3040 9 p. |
artikel |
27 |
Synthesis and activity studies of analogues of the rat selective toxicant norbormide
|
Rennison, David |
|
2007 |
15 |
8 |
p. 2963-2974 12 p. |
artikel |
28 |
Synthesis and biology of bis-xylosylated dihydroxynaphthalenes
|
Johnsson, Richard |
|
2007 |
15 |
8 |
p. 2868-2877 10 p. |
artikel |
29 |
Synthesis and recognition of novel isonucleoside triphosphates by DNA polymerases
|
Jiang, Caiwu |
|
2007 |
15 |
8 |
p. 3019-3025 7 p. |
artikel |
30 |
Synthesis, determination of the absolute configuration of tonkinelin, and inhibitory action with bovine heart mitochondrial complex I
|
Hattori, Yasunao |
|
2007 |
15 |
8 |
p. 3026-3031 6 p. |
artikel |
31 |
Synthesis of a novel C2-aryl pyrrolo[2,1-c][1,4]benzodiazepine-5,11-dione library: Effect of C2-aryl substitution on cytotoxicity and non-covalent DNA binding
|
Antonow, Dyeison |
|
2007 |
15 |
8 |
p. 3041-3053 13 p. |
artikel |
32 |
Synthesis of 3-[4′-(p-chlorophenyl)-thiazol-2′-yl]-2-[(substituted azetidinone/thiazolidinone)-aminomethyl]-6-bromoquinazolin-4-ones as anti-inflammatory agent
|
Kumar, Ashok |
|
2007 |
15 |
8 |
p. 3089-3096 8 p. |
artikel |
33 |
Synthesis of xanthone derivatives with extended π-systems as α-glucosidase inhibitors: Insight into the probable binding mode
|
Liu, Yan |
|
2007 |
15 |
8 |
p. 2810-2814 5 p. |
artikel |
34 |
The use of aminoglycoside derivatives to study the mechanism of aminoglycoside 6′-N-acetyltransferase and the role of 6′-NH2 in antibacterial activity
|
Yan, Xuxu |
|
2007 |
15 |
8 |
p. 2944-2951 8 p. |
artikel |