| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Actions between neonicotinoids and key residues of insect nAChR based on an ab initio quantum chemistry study: Hydrogen bonding and cooperative π–π interaction
|
Wang, Yanli
|
|
2007
|
15 |
7 |
p. 2624-2630
7 p.
|
artikel
|
| 2 |
Amphipathic benzoic acid derivatives: Synthesis and binding in the hydrophobic tunnel of the zinc deacetylase LpxC
|
Shin, Hyunshun
|
|
2007
|
15 |
7 |
p. 2617-2623
7 p.
|
artikel
|
| 3 |
A new modification of anti-tubercular active molecules
|
Imramovský, Aleš
|
|
2007
|
15 |
7 |
p. 2551-2559
9 p.
|
artikel
|
| 4 |
Antituberculosis drugs: Ten years of research
|
Janin, Yves L.
|
|
2007
|
15 |
7 |
p. 2479-2513
35 p.
|
artikel
|
| 5 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2007
|
15 |
7 |
p. 2797-2799
3 p.
|
artikel
|
| 6 |
Clubbed thiazoles by MAOS: A novel approach to cyclin-dependent kinase 5/p25 inhibitors as a potential treatment for Alzheimer’s disease
|
Shiradkar, Mahendra Ramesh
|
|
2007
|
15 |
7 |
p. 2601-2610
10 p.
|
artikel
|
| 7 |
Comparative rates of sialylation by recombinant trans-sialidase and inhibitor properties of synthetic oligosaccharides from Trypanosoma cruzi mucins-containing galactofuranose and galactopyranose
|
Agustí, Rosalía
|
|
2007
|
15 |
7 |
p. 2611-2616
6 p.
|
artikel
|
| 8 |
Design and synthesis of long-acting inhibitors of dipeptidyl peptidase IV
|
Kondo, Takashi
|
|
2007
|
15 |
7 |
p. 2715-2735
21 p.
|
artikel
|
| 9 |
Design and synthesis of new potent dipeptidyl peptidase IV inhibitors with enhanced ex vivo duration
|
Kondo, Takashi
|
|
2007
|
15 |
7 |
p. 2631-2650
20 p.
|
artikel
|
| 10 |
Design, synthesis, and evaluation of non-steroidal farnesoid X receptor (FXR) antagonist
|
Kainuma, Masahiko
|
|
2007
|
15 |
7 |
p. 2587-2600
14 p.
|
artikel
|
| 11 |
Design, synthesis, inhibitory activity, and SAR studies of pyrrolidine derivatives as neuraminidase inhibitors
|
Zhang, Jie
|
|
2007
|
15 |
7 |
p. 2749-2758
10 p.
|
artikel
|
| 12 |
Dibenzothiazoles as novel amyloid-imaging agents
|
Wu, Chunying
|
|
2007
|
15 |
7 |
p. 2789-2796
8 p.
|
artikel
|
| 13 |
Discovery of 1,4-dihydroindeno[1,2-c]pyrazoles as a novel class of potent and selective checkpoint kinase 1 inhibitors
|
Tong, Yunsong
|
|
2007
|
15 |
7 |
p. 2759-2767
9 p.
|
artikel
|
| 14 |
Editorial board
|
|
|
2007
|
15 |
7 |
p. IFC-
1 p.
|
artikel
|
| 15 |
Exploration of the correlation between the structure, hemolytic activity, and cytotoxicity of steroid saponins
|
Wang, Yibing
|
|
2007
|
15 |
7 |
p. 2528-2532
5 p.
|
artikel
|
| 16 |
Graphical contents list
|
|
|
2007
|
15 |
7 |
p. 2471-2478
8 p.
|
artikel
|
| 17 |
Identification of tyrosinase inhibitors from Marrubium velutinum and Marrubium cylleneum
|
Karioti, Anastasia
|
|
2007
|
15 |
7 |
p. 2708-2714
7 p.
|
artikel
|
| 18 |
Instructions to contributors
|
|
|
2007
|
15 |
7 |
p. I-
1 p.
|
artikel
|
| 19 |
Naphthoindole-based analogues of tryptophan and tryptamine: Synthesis and cytotoxic properties
|
Shchekotikhin, Andrey E.
|
|
2007
|
15 |
7 |
p. 2651-2659
9 p.
|
artikel
|
| 20 |
N6-[(Hetero)aryl/(cyclo)alkyl-carbamoyl-methoxy-phenyl]-(2-chloro)-5′-N-ethylcarboxamido-adenosines: The first example of adenosine-related structures with potent agonist activity at the human A2B adenosine receptor
|
Baraldi, Pier Giovanni
|
|
2007
|
15 |
7 |
p. 2514-2527
14 p.
|
artikel
|
| 21 |
Novel chiral isoxazole derivatives: Synthesis and pharmacological characterization at human β-adrenergic receptor subtypes
|
Dallanoce, Clelia
|
|
2007
|
15 |
7 |
p. 2533-2543
11 p.
|
artikel
|
| 22 |
Novel 3-iodo-8-ethoxypyrazolo[5,1-c][1,2,4]benzotriazine 5-oxide as promising lead for design of α5-inverse agonist useful tools for therapy of mnemonic damage
|
Guerrini, Gabriella
|
|
2007
|
15 |
7 |
p. 2573-2586
14 p.
|
artikel
|
| 23 |
On the applicability of QSAR for recognition of miRNA bioorganic structures at early stages of organism and cell development: Embryo and stem cells
|
González-Díaz, Humberto
|
|
2007
|
15 |
7 |
p. 2544-2550
7 p.
|
artikel
|
| 24 |
Optimization and determination of the absolute configuration of a series of potent inhibitors of human papillomavirus type-11 E1–E2 protein–protein interaction: A combined medicinal chemistry, NMR and computational chemistry approach
|
Goudreau, Nathalie
|
|
2007
|
15 |
7 |
p. 2690-2700
11 p.
|
artikel
|
| 25 |
QSAR analysis for heterocyclic antifungals
|
Duchowicz, Pablo R.
|
|
2007
|
15 |
7 |
p. 2680-2689
10 p.
|
artikel
|
| 26 |
Second generation of 5-ethenylbenzofuroxan derivatives as inhibitors of Trypanosoma cruzi growth: Synthesis, biological evaluation, and structure–activity relationships
|
Porcal, Williams
|
|
2007
|
15 |
7 |
p. 2768-2781
14 p.
|
artikel
|
| 27 |
Synthesis and antiplasmodial activity of new N-[3-(4-{3-[(7-chloroquinolin-4-yl)amino]propyl}piperazin-1-yl)propyl]carboxamides
|
Freitag, Marcus
|
|
2007
|
15 |
7 |
p. 2782-2788
7 p.
|
artikel
|
| 28 |
Synthesis of dioxane-based antiviral agents and evaluation of their biological activities as inhibitors of Sindbis virus replication
|
Kim, Ha Young
|
|
2007
|
15 |
7 |
p. 2667-2679
13 p.
|
artikel
|
| 29 |
Synthesis of dl-standishinal and its related compounds for the studies on structure–activity relationship of inhibitory activity against aromatase
|
Katoh, Takahiro
|
|
2007
|
15 |
7 |
p. 2736-2748
13 p.
|
artikel
|
| 30 |
Synthesis of S-dialkylarsino-3-mercapto-1,2-propanediols and evaluation of their anticancer activity
|
Gao, Mingzhang
|
|
2007
|
15 |
7 |
p. 2660-2666
7 p.
|
artikel
|
| 31 |
Synthesis, structural characterization, and in vitro antitumor activity of novel N-(6-chloro-1,1-dioxo-1,4,2-benzodithiazin-3-yl)arylsulfonamides
|
Brzozowski, Zdzisław
|
|
2007
|
15 |
7 |
p. 2560-2572
13 p.
|
artikel
|
| 32 |
The synthesis of α,β-unsaturated carbonyl derivatives with the ability to inhibit both glutathione S-transferase P1-1 activity and the proliferation of leukemia cells
|
Zhao, Guisen
|
|
2007
|
15 |
7 |
p. 2701-2707
7 p.
|
artikel
|
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