| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
3-Amino-2(5H)furanones as inhibitors of subgenomic hepatitis C virus RNA replication
|
Iannazzo, Daniela
|
|
2008
|
16 |
21 |
p. 9610-9615
6 p.
|
artikel
|
| 2 |
An endoplasmic reticulum (ER) stress-suppressive compound and its analogues from the mushroom Hericium erinaceum
|
Ueda, Keiko
|
|
2008
|
16 |
21 |
p. 9467-9470
4 p.
|
artikel
|
| 3 |
Anti-inflammatory activities of furanoditerpenoids and other constituents from Fibraurea tinctoria
|
Su, Chung-Ren
|
|
2008
|
16 |
21 |
p. 9603-9609
7 p.
|
artikel
|
| 4 |
Anti-inflammatory properties of a heparin-like glycosaminoglycan with reduced anti-coagulant activity isolated from a marine shrimp
|
Brito, Adriana S.
|
|
2008
|
16 |
21 |
p. 9588-9595
8 p.
|
artikel
|
| 5 |
Axial chirality and affinity at the GABAA receptor of pyrimido[1,2-a][1,4]benzodiazepines and related compounds
|
Lee, Shoukou
|
|
2008
|
16 |
21 |
p. 9519-9523
5 p.
|
artikel
|
| 6 |
2,2′-Bipyridinebutyldithiocarbamatoplatinum(II) and palladium(II) complexes: Synthesis, characterization, cytotoxicity, and rich DNA-binding studies
|
Mansouri-Torshizi, Hassan
|
|
2008
|
16 |
21 |
p. 9616-9625
10 p.
|
artikel
|
| 7 |
Building skeletally diverse architectures on the Indoline Scaffold: The discovery of a chemical probe of focal adhesion kinase signaling networks
|
Prakesch, Michael
|
|
2008
|
16 |
21 |
p. 9596-9602
7 p.
|
artikel
|
| 8 |
Design, synthesis and SAR of potent statine-based BACE-1 inhibitors: Exploration of P1 phenoxy and benzyloxy residues
|
Bäck, Marcus
|
|
2008
|
16 |
21 |
p. 9471-9486
16 p.
|
artikel
|
| 9 |
Editorial board
|
|
|
2008
|
16 |
21 |
p. IFC-
1 p.
|
artikel
|
| 10 |
Evaluation of peptide-aldehyde inhibitors using R188I mutant of SARS 3CL protease as a proteolysis-resistant mutant
|
Akaji, Kenichi
|
|
2008
|
16 |
21 |
p. 9400-9408
9 p.
|
artikel
|
| 11 |
Graphical contents list
|
|
|
2008
|
16 |
21 |
p. 9393-9399
7 p.
|
artikel
|
| 12 |
Hedgehog/GLI-mediated transcriptional inhibitors from Zizyphus cambodiana
|
Arai, Midori A.
|
|
2008
|
16 |
21 |
p. 9420-9424
5 p.
|
artikel
|
| 13 |
Influence of 6- or 8-substitution on the antiviral activity of 3-arylalkylthiomethylimidazo[1,2-a]pyridine against human cytomegalovirus (CMV) and varicella-zoster virus (VZV): Part II
|
Véron, Jean-Baptiste
|
|
2008
|
16 |
21 |
p. 9536-9545
10 p.
|
artikel
|
| 14 |
Inhibition of the CRM1-mediated nucleocytoplasmic transport by N-azolylacrylates: Structure–activity relationship and mechanism of action
|
Van Neck, Tine
|
|
2008
|
16 |
21 |
p. 9487-9497
11 p.
|
artikel
|
| 15 |
Instructions to contributors
|
|
|
2008
|
16 |
21 |
p. I-
1 p.
|
artikel
|
| 16 |
Investigations toward the selection of fully-modified 4′-thioRNA aptamers: Optimization of in vitro transcription steps in the presence of 4′-thioNTPs
|
Minakawa, Noriaki
|
|
2008
|
16 |
21 |
p. 9450-9456
7 p.
|
artikel
|
| 17 |
Molecular dynamics simulations of the amyloid-beta binding alcohol dehydrogenase (ABAD) enzyme
|
Marques, Alexandra T.
|
|
2008
|
16 |
21 |
p. 9511-9518
8 p.
|
artikel
|
| 18 |
Novel potent and selective Ca2+ release-activated Ca2+ (CRAC) channel inhibitors. Part 3: Synthesis and CRAC channel inhibitory activity of 4′-[(trifluoromethyl)pyrazol-1-yl]carboxanilides
|
Yonetoku, Yasuhiro
|
|
2008
|
16 |
21 |
p. 9457-9466
10 p.
|
artikel
|
| 19 |
Preparation of (4,4-difluoro-1,2,3,4-tetrahydro-5H-1-benzazepin-5-ylidene)acetamide derivatives as novel arginine vasopressin V2 receptor agonists
|
Tsukamoto, Issei
|
|
2008
|
16 |
21 |
p. 9524-9535
12 p.
|
artikel
|
| 20 |
Site specific chemical delivery of NSAIDs to inflamed joints: Synthesis, biological activity and γ-imaging studies of quaternary ammonium salts of tropinol esters of some NSAIDs or their active metabolites
|
Yadav, Mange Ram
|
|
2008
|
16 |
21 |
p. 9443-9449
7 p.
|
artikel
|
| 21 |
(3S)-N-(l-Aminoacyl)-1,2,3,4-tetrahydroisoquinolines, a class of novel antithrombotic agents: Synthesis, bioassay, 3D QSAR, and ADME analysis
|
Zheng, Meiqing
|
|
2008
|
16 |
21 |
p. 9574-9587
14 p.
|
artikel
|
| 22 |
Synthesis and anti-inflammatory structure–activity relationships of thiazine–quinoline–quinones: Inhibitors of the neutrophil respiratory burst in a model of acute gouty arthritis
|
Chia, Elizabeth W.
|
|
2008
|
16 |
21 |
p. 9432-9442
11 p.
|
artikel
|
| 23 |
Synthesis and antitubercular activity of ferrocenyl diaminoalcohols and diamines
|
Andrianina Ralambomanana, Dimby
|
|
2008
|
16 |
21 |
p. 9546-9553
8 p.
|
artikel
|
| 24 |
Synthesis, biological evaluation, and molecular modeling investigation of chiral 2-(4-chloro-phenoxy)-3-phenyl-propanoic acid derivatives with PPARα and PPARγ agonist activity
|
Fracchiolla, Giuseppe
|
|
2008
|
16 |
21 |
p. 9498-9510
13 p.
|
artikel
|
| 25 |
Synthesis, biological evaluation, structural–activity relationship, and docking study for a series of benzoxepin-derived estrogen receptor modulators
|
Barrett, Irene
|
|
2008
|
16 |
21 |
p. 9554-9573
20 p.
|
artikel
|
| 26 |
Synthesis of new pyrazolo[5,1-c][1,2,4] benzotriazines, pyrazolo[5,1-c]pyrido[4,3-e][1,2,4] triazines and their open analogues as cytotoxic agents in normoxic and hypoxic conditions
|
Ciciani, Giovanna
|
|
2008
|
16 |
21 |
p. 9409-9419
11 p.
|
artikel
|
| 27 |
Synthesis of 6-substituted 1-phenylbenzazepines and their dopamine D1 receptor activities
|
Zhang, Jing
|
|
2008
|
16 |
21 |
p. 9425-9431
7 p.
|
artikel
|
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