| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A peptoid antagonist of VEGF Receptor 2 recognizes a ‘hotspot’ in the extracellular domain distinct from the hormone-binding site
|
Udugamasooriya, D. Gomika
|
|
2008
|
16 |
12 |
p. 6338-6343
6 p.
|
artikel
|
| 2 |
Aroyl hydrazones of 2-phenylindole-3-carbaldehydes as novel antimitotic agents
|
Vogel, Susanne
|
|
2008
|
16 |
12 |
p. 6436-6447
12 p.
|
artikel
|
| 3 |
Carbon-11 labeled indolylpropylamine analog as a new potential PET agent for imaging of the serotonin transporter
|
Ben-Daniel, R.
|
|
2008
|
16 |
12 |
p. 6364-6370
7 p.
|
artikel
|
| 4 |
Chemometric and chemoinformatic analyses of anabolic and androgenic activities of testosterone and dihydrotestosterone analogues
|
Alvarez-Ginarte, Yoanna María
|
|
2008
|
16 |
12 |
p. 6448-6459
12 p.
|
artikel
|
| 5 |
Design, synthesis and biological evaluation of bis(hydroxyphenyl) azoles as potent and selective non-steroidal inhibitors of 17β-hydroxysteroid dehydrogenase type 1 (17β-HSD1) for the treatment of estrogen-dependent diseases
|
Bey, Emmanuel
|
|
2008
|
16 |
12 |
p. 6423-6435
13 p.
|
artikel
|
| 6 |
Design, synthesis and spectroscopic studies of resveratrol aliphatic acid ligands of human serum albumin
|
Jiang, Yu Lin
|
|
2008
|
16 |
12 |
p. 6406-6414
9 p.
|
artikel
|
| 7 |
Discovery of potent furan piperazine sodium channel blockers for treatment of neuropathic pain
|
Drizin, Irene
|
|
2008
|
16 |
12 |
p. 6379-6386
8 p.
|
artikel
|
| 8 |
Duocarmycin-based prodrugs for cancer prodrug monotherapy
|
Tietze, Lutz F.
|
|
2008
|
16 |
12 |
p. 6312-6318
7 p.
|
artikel
|
| 9 |
Editorial board
|
|
|
2008
|
16 |
12 |
p. IFC-
1 p.
|
artikel
|
| 10 |
Graphical contents list
|
|
|
2008
|
16 |
12 |
p. 6307-6311
5 p.
|
artikel
|
| 11 |
Hybrids of 1-deoxynojirimycin and aryl-1,2,3-triazoles and biological studies related to angiogenesis
|
Zhao, Yunxue
|
|
2008
|
16 |
12 |
p. 6333-6337
5 p.
|
artikel
|
| 12 |
Instructions to contributors
|
|
|
2008
|
16 |
12 |
p. I-
1 p.
|
artikel
|
| 13 |
Novel Azabicyclo[3.2.2]nonane derivatives and their activities against Plasmodium falciparum K1 and Trypanosoma brucei rhodesiense
|
Berger, Heinrich
|
|
2008
|
16 |
12 |
p. 6371-6378
8 p.
|
artikel
|
| 14 |
Parallel one-pot synthesis and structure–activity relationship study of symmetric formimidoester disulfides as a novel class of potent non-nucleoside HIV-1 reverse transcriptase inhibitors
|
Cesarini, Sara
|
|
2008
|
16 |
12 |
p. 6353-6363
11 p.
|
artikel
|
| 15 |
Structure–activity relationships of a peptide inhibitor of the human FcRn:human IgG interaction
|
Mezo, Adam R.
|
|
2008
|
16 |
12 |
p. 6394-6405
12 p.
|
artikel
|
| 16 |
Structure–activity study of endomorphin-2 analogs with C-terminal modifications by NMR spectroscopy and molecular modeling
|
Wang, Chang-lin
|
|
2008
|
16 |
12 |
p. 6415-6422
8 p.
|
artikel
|
| 17 |
Synthesis and analgesic/anti-inflammatory evaluation of fused heterocyclic ring systems incorporating phenylsulfonyl moiety
|
Shaaban, Mohamed R.
|
|
2008
|
16 |
12 |
p. 6344-6352
9 p.
|
artikel
|
| 18 |
Synthesis and in vitro biological activity of retinyl retinoate, a novel hybrid retinoid derivative
|
Kim, Hyojung
|
|
2008
|
16 |
12 |
p. 6387-6393
7 p.
|
artikel
|
| 19 |
Synthesis and potency of novel uracil nucleotides and derivatives as P2Y2 and P2Y6 receptor agonists
|
Ko, Hyojin
|
|
2008
|
16 |
12 |
p. 6319-6332
14 p.
|
artikel
|
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