| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A formyl peptide substituted with a conformationally constrained phenylalanine residue evokes a selective immune response in human neutrophils
|
Hayashi, Ryo
|
|
2013
|
21 |
3 |
p. 668-675
8 p.
|
artikel
|
| 2 |
Alkaloid constituents from flower buds and leaves of sacred lotus (Nelumbo nucifera, Nymphaeaceae) with melanogenesis inhibitory activity in B16 melanoma cells
|
Nakamura, Seikou
|
|
2013
|
21 |
3 |
p. 779-787
9 p.
|
artikel
|
| 3 |
Automated parallel synthesis of 5′-triphosphate oligonucleotides and preparation of chemically modified 5′-triphosphate small interfering RNA
|
Zlatev, Ivan
|
|
2013
|
21 |
3 |
p. 722-732
11 p.
|
artikel
|
| 4 |
Biocatalytic synthesis, structural elucidation, antioxidant capacity and tyrosinase inhibition activity of long chain fatty acid acylated derivatives of phloridzin and isoquercitrin
|
Ziaullah,
|
|
2013
|
21 |
3 |
p. 684-692
9 p.
|
artikel
|
| 5 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2013
|
21 |
3 |
p. I-III
nvt p.
|
artikel
|
| 6 |
Chemical, biochemical and microbiological properties of a brominated nitrovinylfuran with broad-spectrum antibacterial activity
|
Scholz, Therese
|
|
2013
|
21 |
3 |
p. 795-804
10 p.
|
artikel
|
| 7 |
Conjugation to 4-aminoquinoline improves the anti-trypanosomal activity of Deferiprone-type iron chelators
|
Gehrke, Sebastian S.
|
|
2013
|
21 |
3 |
p. 805-813
9 p.
|
artikel
|
| 8 |
Corrigendum to ‘Discovery and pharmacological characterization of N[2-({2-[(2S)-2-cyanopyrrolidin-1-yl]-2-oxoethyl}amino)-2 methylpropyl]-2-methylpyrazolo[1,5-a]pyrimidine-6-carboxamide hydrochloride (anagliptin hydrochloride salt) as a potent and selective DPP-IV inhibitor’ [Bioorg. Med. Chem. 19 (2011) 7221–7227]
|
Kato, Noriyasu
|
|
2013
|
21 |
3 |
p. 832-833
2 p.
|
artikel
|
| 9 |
Corrigendum to “The biology and chemistry of antifungal agents: A review” [Bioorg. Med. Chem. 20 (2012) 5678–5698]
|
Kathiravan, Muthu K.
|
|
2013
|
21 |
3 |
p. 834-
1 p.
|
artikel
|
| 10 |
Design, synthesis and biological evaluation of novel aliphatic amido/sulfonamido-quaternary ammonium salts as antitumor agents
|
Song, Doona
|
|
2013
|
21 |
3 |
p. 788-794
7 p.
|
artikel
|
| 11 |
Design, synthesis and evaluation of novel heterodimers of donepezil and huperzine fragments as acetylcholinesterase inhibitors
|
Hu, Yueqing
|
|
2013
|
21 |
3 |
p. 676-683
8 p.
|
artikel
|
| 12 |
Design, synthesis, and structure–activity relationship (SAR) of N-[7-(4-hydroxyphenoxy)-6-methylindan-4-yl]malonamic acids as thyroid hormone receptor β (TRβ) selective agonists
|
Shiohara, Hiroaki
|
|
2013
|
21 |
3 |
p. 592-607
16 p.
|
artikel
|
| 13 |
Design, synthesis, and structure–activity relationships of a series of 4-benzyl-5-isopropyl-1H-pyrazol-3-yl β-d-glycopyranosides substituted with novel hydrophilic groups as highly potent inhibitors of sodium glucose co-transporter 1 (SGLT1)
|
Fushimi, Nobuhiko
|
|
2013
|
21 |
3 |
p. 748-765
18 p.
|
artikel
|
| 14 |
Editorial board
|
|
|
2013
|
21 |
3 |
p. IFC-
1 p.
|
artikel
|
| 15 |
Effects of fluorines on nonsecosteroidal vitamin D receptor agonists
|
Kashiwagi, Hirotaka
|
|
2013
|
21 |
3 |
p. 712-721
10 p.
|
artikel
|
| 16 |
Enhanced bioactivity of silybin B methylation products
|
Sy-Cordero, Arlene A.
|
|
2013
|
21 |
3 |
p. 742-747
6 p.
|
artikel
|
| 17 |
Exploration of 1-(3-chloro-4-(4-oxo-4H-chromen-2-yl)phenyl)-3-phenylurea derivatives as selective dual inhibitors of Raf1 and JNK1 kinases for anti-tumor treatment
|
Jin, Feng
|
|
2013
|
21 |
3 |
p. 824-831
8 p.
|
artikel
|
| 18 |
Graphical contents list
|
|
|
2013
|
21 |
3 |
p. 569-576
8 p.
|
artikel
|
| 19 |
Investigations into the synthesis, radiofluorination and conjugation of a new [18F]fluorocyclobutyl prosthetic group and its in vitro stability using a tyrosine model system
|
Franck, Dominic
|
|
2013
|
21 |
3 |
p. 643-652
10 p.
|
artikel
|
| 20 |
Molecular recognition of indole derivatives by polymers imprinted with indole-3-acetic acid: A QSPR study
|
Porobić, Ivana
|
|
2013
|
21 |
3 |
p. 653-659
7 p.
|
artikel
|
| 21 |
Recent development of potent analogues of oxazolidinone antibacterial agents
|
Michalska, Katarzyna
|
|
2013
|
21 |
3 |
p. 577-591
15 p.
|
artikel
|
| 22 |
SiO2 nanoparticles as platform for delivery of nucleoside triphosphate analogues into cells
|
Vasilyeva, Svetlana V.
|
|
2013
|
21 |
3 |
p. 703-711
9 p.
|
artikel
|
| 23 |
Small-molecular, non-peptide, non-ATP-competitive polo-like kinase 1 (Plk1) inhibitors with a terphenyl skeleton
|
Mita, Yusuke
|
|
2013
|
21 |
3 |
p. 608-617
10 p.
|
artikel
|
| 24 |
Structure-based drug design and potent anti-cancer activity of tricyclic 5:7:5-fused diimidazo[4,5-d:4′,5′-f][1,3]diazepines
|
Kondaskar, Atul
|
|
2013
|
21 |
3 |
p. 618-631
14 p.
|
artikel
|
| 25 |
Synthesis and biological evaluation of halogenated curcumin analogs as potential nuclear receptor selective agonists
|
Batie, Shane
|
|
2013
|
21 |
3 |
p. 693-702
10 p.
|
artikel
|
| 26 |
Synthesis and biological evaluation of N-alkyl-N-(4-methoxyphenyl)pyridin-2-amines as a new class of tubulin polymerization inhibitors
|
Wang, Xiao-Feng
|
|
2013
|
21 |
3 |
p. 632-642
11 p.
|
artikel
|
| 27 |
Synthesis and evaluation of thiazolidinedione and dioxazaborocane analogues as inhibitors of AI-2 quorum sensing in Vibrio harveyi
|
Brackman, Gilles
|
|
2013
|
21 |
3 |
p. 660-667
8 p.
|
artikel
|
| 28 |
Synthesis of 13C-labeled and functionalized Hyaluronan derivatives for biophysical studies and surface modifications
|
Rigol, Stephan
|
|
2013
|
21 |
3 |
p. 733-741
9 p.
|
artikel
|
| 29 |
Synthesis, topoisomerase-targeting activity and growth inhibition of lycobetaine analogs
|
Baechler, Simone A.
|
|
2013
|
21 |
3 |
p. 814-823
10 p.
|
artikel
|
| 30 |
The discovery of novel isoflavone pan peroxisome proliferator-activated receptor agonists
|
Matin, Azadeh
|
|
2013
|
21 |
3 |
p. 766-778
13 p.
|
artikel
|
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