Digitale Bibliotheek
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                             26 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Acetylcholine binding protein (AChBP) as template for hierarchical in silico screening procedures to identify structurally novel ligands for the nicotinic receptors Akdemir, Atilla
2011
19 20 p. 6107-6119
13 p.
artikel
2 Anti-obesity effects of the methanolic extract and chakasaponins from the flower buds of Camellia sinensis in mice Hamao, Makoto
2011
19 20 p. 6033-6041
9 p.
artikel
3 Design, synthesis and biological evaluation of novel 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid derivatives as aminopeptidase N/CD13 inhibitors Zhang, Xiaopan
2011
19 20 p. 6015-6025
11 p.
artikel
4 Design, synthesis and vasorelaxant evaluation of novel coumarin–pyrimidine hybrids Amin, Kamilia M.
2011
19 20 p. 6087-6097
11 p.
artikel
5 Does the combination of optimal substitutions at the C2-, N5- and N8-positions of the pyrazolo-triazolo-pyrimidine scaffold guarantee selective modulation of the human A3 adenosine receptors? Cheong, Siew Lee
2011
19 20 p. 6120-6134
15 p.
artikel
6 Editorial board 2011
19 20 p. IFC-
1 p.
artikel
7 5-Fluoro-4-thiouridine phosphoramidite: New synthon for introducing photoaffinity label into oligodeoxynucleotides Milecki, Jan
2011
19 20 p. 6098-6106
9 p.
artikel
8 Graphical contents list 2011
19 20 p. 5917-5923
7 p.
artikel
9 Inhibition of steroid sulfatase with 4-substituted estrone and estradiol derivatives Phan, Chau-Minh
2011
19 20 p. 5999-6005
7 p.
artikel
10 Lead identification of β-lactam and related imine inhibitors of the molecular chaperone heat shock protein 90 O’Boyle, Niamh M.
2011
19 20 p. 6055-6068
14 p.
artikel
11 Metronidazole acid acyl sulfonamide: A novel class of anticancer agents and potential EGFR tyrosine kinase inhibitors Luo, Yin
2011
19 20 p. 6069-6076
8 p.
artikel
12 Novel diarylpyridinones, diarylpyridazinones and diarylphthalazinones as potential HIV-1 nonnucleoside reverse transcriptase inhibitors (NNRTIs) Venkatraj, Muthusamy
2011
19 20 p. 5924-5934
11 p.
artikel
13 Novel human mPGES-1 inhibitors identified through structure-based virtual screening Hamza, Adel
2011
19 20 p. 6077-6086
10 p.
artikel
14 Potent inhibition of Norwalk virus by cyclic sulfamide derivatives Dou, Dengfeng
2011
19 20 p. 5975-5983
9 p.
artikel
15 Pyrazolo[1,5-a]pyrimidines, triazolo[1,5-a]pyrimidines and their tricyclic derivatives as corticotropin-releasing factor 1 (CRF1) receptor antagonists Saito, Tetsuji
2011
19 20 p. 5955-5966
12 p.
artikel
16 Solid-state NMR analysis of interaction sites of curcumin and 42-residue amyloid β-protein fibrils Masuda, Yuichi
2011
19 20 p. 5967-5974
8 p.
artikel
17 Structural requirement of arylindolylpropenones as anti-bladder carcinoma cells agents Martel-Frachet, Véronique
2011
19 20 p. 6143-6148
6 p.
artikel
18 Structure-based design of dipeptide derivatives for the human neutral endopeptidase Misawa, Kensuke
2011
19 20 p. 5935-5947
13 p.
artikel
19 Synthesis and anticonvulsant activity of new N-Mannich bases derived from 5-cyclopropyl-5-phenyl- and 5-cyclopropyl-5-(4-chlorophenyl)-imidazolidine-2,4-diones Byrtus, Hanna
2011
19 20 p. 6149-6156
8 p.
artikel
20 Synthesis and antitumor activity of 1,2,4-triazoles having 1,4-benzodioxan fragment as a novel class of potent methionine aminopeptidase type II inhibitors Hou, Ya-Ping
2011
19 20 p. 5948-5954
7 p.
artikel
21 Synthesis and biological evaluation of a novel class of isatin analogs as dual inhibitors of tubulin polymerization and Akt pathway Krishnegowda, Gowdahalli
2011
19 20 p. 6006-6014
9 p.
artikel
22 Synthesis and biological evaluation of new opioid agonist and neurokinin-1 antagonist bivalent ligands Vardanyan, Ruben
2011
19 20 p. 6135-6142
8 p.
artikel
23 Synthesis and biological evaluation of phenstatin metabolites Ghinet, Alina
2011
19 20 p. 6042-6054
13 p.
artikel
24 Synthesis of a series of 3,4-methanoarginines as side-chain conformationally restricted analogues of arginine Watanabe, Mizuki
2011
19 20 p. 5984-5988
5 p.
artikel
25 The discovery of long-acting saligenin β2 adrenergic receptor agonists incorporating a urea group Procopiou, Panayiotis A.
2011
19 20 p. 6026-6032
7 p.
artikel
26 The effect of a bromide leaving group on the properties of nitro analogs of the duocarmycins as hypoxia-activated prodrugs and phosphate pre-prodrugs for antitumor therapy Stevenson, Ralph J.
2011
19 20 p. 5989-5998
10 p.
artikel
                             26 gevonden resultaten
 
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