| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel application of DDQ as electrophile in the Nenitzescu reaction
|
Kucklaender, U.
|
|
2011
|
19 |
8 |
p. 2666-2674
9 p.
|
artikel
|
| 2 |
Anti-tumor and anti-leishmanial evaluations of 1,3,4-oxadiazine, pyran derivatives derived from cross-coupling reactions of β-bromo-6H-1,3,4-oxadiazine derivatives
|
Mohareb, Rafat M.
|
|
2011
|
19 |
8 |
p. 2707-2713
7 p.
|
artikel
|
| 3 |
7-Azabicyclo[2.2.1]heptane as a structural motif to block mutagenicity of nitrosamines
|
Ohwada, Tomohiko
|
|
2011
|
19 |
8 |
p. 2726-2741
16 p.
|
artikel
|
| 4 |
Cytotoxic and anti-inflammatory cembranoids from the Vietnamese soft coral Lobophytum laevigatum
|
Quang, Tran Hong
|
|
2011
|
19 |
8 |
p. 2625-2632
8 p.
|
artikel
|
| 5 |
Design, synthesis, and evaluation of small molecule Hsp90 probes
|
Taldone, Tony
|
|
2011
|
19 |
8 |
p. 2603-2614
12 p.
|
artikel
|
| 6 |
Design, synthesis, and structure–activity relationship studies of thiophene-3-carboxamide derivatives as dual inhibitors of the c-Jun N-terminal kinase
|
De, Surya K.
|
|
2011
|
19 |
8 |
p. 2582-2588
7 p.
|
artikel
|
| 7 |
Diphenylamine-based retinoid antagonists: Regulation of RAR and RXR function depending on the N-substituent
|
Ohta, Kiminori
|
|
2011
|
19 |
8 |
p. 2501-2507
7 p.
|
artikel
|
| 8 |
Editorial board
|
|
|
2011
|
19 |
8 |
p. IFC-
1 p.
|
artikel
|
| 9 |
Extending SAR of bile acids as FXR ligands: Discovery of 23-N-(carbocinnamyloxy)-3α,7α-dihydroxy-6α-ethyl-24-nor-5β-cholan-23-amine
|
Gioiello, Antimo
|
|
2011
|
19 |
8 |
p. 2650-2658
9 p.
|
artikel
|
| 10 |
Fluorescent cyclin-dependent kinase inhibitors block the proliferation of human breast cancer cells
|
Yenugonda, Venkata Mahidhar
|
|
2011
|
19 |
8 |
p. 2714-2725
12 p.
|
artikel
|
| 11 |
Fluorescent phosphoinositide 3-kinase inhibitors suitable for monitoring of intracellular distribution
|
Kim, Donghee
|
|
2011
|
19 |
8 |
p. 2508-2516
9 p.
|
artikel
|
| 12 |
Fused heterocyclic amido compounds as anti-hepatitis C virus agents
|
Aoyama, Hiroshi
|
|
2011
|
19 |
8 |
p. 2675-2687
13 p.
|
artikel
|
| 13 |
Geminal dialkyl derivatives of N-substituted pantothenamides: Synthesis and antibacterial activity
|
Akinnusi, T. Olukayode
|
|
2011
|
19 |
8 |
p. 2696-2706
11 p.
|
artikel
|
| 14 |
Graphical contents list
|
|
|
2011
|
19 |
8 |
p. 2485-2493
9 p.
|
artikel
|
| 15 |
Inhibition of amyloid-β aggregation by coumarin analogs can be manipulated by functionalization of the aromatic center
|
Soto-Ortega, Deborah D.
|
|
2011
|
19 |
8 |
p. 2596-2602
7 p.
|
artikel
|
| 16 |
Inhibitors and promoters of tubulin polymerization: Synthesis and biological evaluation of chalcones and related dienones as potential anticancer agents
|
Dyrager, Christine
|
|
2011
|
19 |
8 |
p. 2659-2665
7 p.
|
artikel
|
| 17 |
Inhibitory effects of Mannich bases of heterocyclic chalcones on NO production by activated RAW 264.7 macrophages and superoxide anion generation and elastase release by activated human neutrophils
|
Reddy, M. Vijaya Bhaskar
|
|
2011
|
19 |
8 |
p. 2751-2756
6 p.
|
artikel
|
| 18 |
Inhibitory properties of 2-substituent-1H-benzimidazole-4-carboxamide derivatives against enteroviruses
|
Xue, Fei
|
|
2011
|
19 |
8 |
p. 2641-2649
9 p.
|
artikel
|
| 19 |
Introduction of aromatic group on 4′-OH of α-GalCer manipulated NKT cell cytokine production
|
Zhang, Wenpeng
|
|
2011
|
19 |
8 |
p. 2767-2776
10 p.
|
artikel
|
| 20 |
In vitro and QSAR studies of cucurbitacins on HepG2 and HSC-T6 liver cell lines
|
Bartalis, Judit
|
|
2011
|
19 |
8 |
p. 2757-2766
10 p.
|
artikel
|
| 21 |
New and more efficient multivalent glyco-ligands for asialoglycoprotein receptor of mammalian hepatocytes
|
Lee, Reiko T.
|
|
2011
|
19 |
8 |
p. 2494-2500
7 p.
|
artikel
|
| 22 |
Polyvalent saccharide-functionalized generation 3 poly(amidoamine) dendrimer–methotrexate conjugate as a potential anticancer agent
|
Zhang, Yuehua
|
|
2011
|
19 |
8 |
p. 2557-2564
8 p.
|
artikel
|
| 23 |
QSAR-based permeability model for drug-like compounds
|
Gozalbes, Rafael
|
|
2011
|
19 |
8 |
p. 2615-2624
10 p.
|
artikel
|
| 24 |
Small molecule antagonists of the urokinase (uPA): urokinase receptor (uPAR) interaction with high reported potencies show only weak effects in cell-based competition assays employing the native uPAR ligand
|
Souza, Melissa De
|
|
2011
|
19 |
8 |
p. 2549-2556
8 p.
|
artikel
|
| 25 |
Small molecule inhibitor of the RPA70 N-terminal protein interaction domain discovered using in silico and in vitro methods
|
Glanzer, Jason G.
|
|
2011
|
19 |
8 |
p. 2589-2595
7 p.
|
artikel
|
| 26 |
Synthesis and biological evaluation of estradiol linked pyrrolo[2,1-c][1,4]benzodiazepine (PBD) conjugates as potential anticancer agents
|
Kamal, Ahmed
|
|
2011
|
19 |
8 |
p. 2565-2581
17 p.
|
artikel
|
| 27 |
Synthesis and biological evaluation of 1-substituted-3(5)-(6-methylpyridin-2-yl)-4-(quinolin-6-yl)pyrazoles as transforming growth factor-β type 1 receptor kinase inhibitors
|
Jin, Cheng Hua
|
|
2011
|
19 |
8 |
p. 2633-2640
8 p.
|
artikel
|
| 28 |
Synthesis and biological evaluation of tetracyclic thienopyridones as antibacterial and antitumor agents
|
Al-Trawneh, Salah A.
|
|
2011
|
19 |
8 |
p. 2541-2548
8 p.
|
artikel
|
| 29 |
Synthesis and characterization of a cell-permeable bimodal contrast agent targeting β-galactosidase
|
Keliris, Aneta
|
|
2011
|
19 |
8 |
p. 2529-2540
12 p.
|
artikel
|
| 30 |
Synthesis and pharmacological evaluation of thieno[2,3-b]pyridine derivatives as novel c-Src inhibitors
|
Pevet, Isabelle
|
|
2011
|
19 |
8 |
p. 2517-2528
12 p.
|
artikel
|
| 31 |
Synthesis, biological evaluation, and molecular docking studies of resveratrol derivatives possessing chalcone moiety as potential antitubulin agents
|
Ruan, Ban-Feng
|
|
2011
|
19 |
8 |
p. 2688-2695
8 p.
|
artikel
|
| 32 |
The synthesis and evaluation of indolylureas as PKCα inhibitors
|
Djung, Jane F.
|
|
2011
|
19 |
8 |
p. 2742-2750
9 p.
|
artikel
|
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