| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A peptide affinity reagent for isolating an intact and catalytically active multi-protein complex from mammalian cells
|
Saathoff, Hinnerk
|
|
2015
|
23 |
5 |
p. 960-965
6 p.
|
artikel
|
| 2 |
Computer-aided discovery of aminopyridines as novel JAK2 inhibitors
|
Zhao, Chao
|
|
2015
|
23 |
5 |
p. 985-995
11 p.
|
artikel
|
| 3 |
Design and synthesis of a novel candidate compound NTI-007 targeting sodium taurocholate cotransporting polypeptide [NTCP]–APOA1–HBx–Beclin1-mediated autophagic pathway in HBV therapy
|
Zhang, Jin
|
|
2015
|
23 |
5 |
p. 976-984
9 p.
|
artikel
|
| 4 |
Design, synthesis, and biological evaluation of air-stable nafuredin-γ analogs as complex I inhibitors
|
Ohtawa, Masaki
|
|
2015
|
23 |
5 |
p. 932-943
12 p.
|
artikel
|
| 5 |
Design, synthesis, and biological evaluation of novel 2-methylpiperazine derivatives as potent CCR5 antagonists
|
Hu, Suwen
|
|
2015
|
23 |
5 |
p. 1157-1168
12 p.
|
artikel
|
| 6 |
Design, synthesis and evaluation of chromone-2-carboxamido-alkylbenzylamines as multifunctional agents for the treatment of Alzheimer’s disease
|
Liu, Qiang
|
|
2015
|
23 |
5 |
p. 911-923
13 p.
|
artikel
|
| 7 |
Dibenzosuberyl substituted polyamines and analogs of clomipramine as effective inhibitors of trypanothione reductase; molecular docking, and assessment of trypanocidal activities
|
O’Sullivan, Mary C.
|
|
2015
|
23 |
5 |
p. 996-1010
15 p.
|
artikel
|
| 8 |
Discovery and structure–activity relationship studies of N6-benzoyladenine derivatives as novel BRD4 inhibitors
|
Noguchi-Yachide, Tomomi
|
|
2015
|
23 |
5 |
p. 953-959
7 p.
|
artikel
|
| 9 |
Discovery of biphenyl-based VEGFR-2 inhibitors. Part 3: Design, synthesis and 3D-QSAR studies
|
Lu, Wen
|
|
2015
|
23 |
5 |
p. 1044-1054
11 p.
|
artikel
|
| 10 |
Discovery of Mer kinase inhibitors by virtual screening using Structural Protein–Ligand Interaction Fingerprints
|
Da, C.
|
|
2015
|
23 |
5 |
p. 1096-1101
6 p.
|
artikel
|
| 11 |
Editorial board
|
|
|
2015
|
23 |
5 |
p. IFC-
1 p.
|
artikel
|
| 12 |
Enantioselective synthesis of dictyoceratin-A (smenospondiol) and -C, hypoxia-selective growth inhibitors from marine sponge
|
Sumii, Yuji
|
|
2015
|
23 |
5 |
p. 966-975
10 p.
|
artikel
|
| 13 |
Graphical contents list
|
|
|
2015
|
23 |
5 |
p. 903-910
8 p.
|
artikel
|
| 14 |
Guanine-based amphiphiles: synthesis, ion transport properties and biological activity
|
Musumeci, Domenica
|
|
2015
|
23 |
5 |
p. 1149-1156
8 p.
|
artikel
|
| 15 |
Naturally occurring polyphenol, morin hydrate, inhibits enzymatic activity of N-methylpurine DNA glycosylase, a DNA repair enzyme with various roles in human disease
|
Dixon, Monica
|
|
2015
|
23 |
5 |
p. 1102-1111
10 p.
|
artikel
|
| 16 |
Radiosynthesis and micro-SPECT analysis of triazole-based RGD integrin ligands as non-peptide molecular imaging probes for angiogenesis
|
Bianchini, Francesca
|
|
2015
|
23 |
5 |
p. 1112-1122
11 p.
|
artikel
|
| 17 |
Rat hormone sensitive lipase inhibition by cyclipostins and their analogs
|
Vasilieva, Elena
|
|
2015
|
23 |
5 |
p. 944-952
9 p.
|
artikel
|
| 18 |
Rational design, synthesis and structure–activity relationships of 4-alkoxy- and 4-acyloxy-phenylethylenethiosemicarbazone analogues as novel tyrosinase inhibitors
|
You, Ao
|
|
2015
|
23 |
5 |
p. 924-931
8 p.
|
artikel
|
| 19 |
Scaffold hopping: Exploration of acetanilide-containing uracil analogues as potential NNRTIs
|
Babkov, Denis A.
|
|
2015
|
23 |
5 |
p. 1069-1081
13 p.
|
artikel
|
| 20 |
Structural development of stapled short helical peptides as vitamin D receptor (VDR)–coactivator interaction inhibitors
|
Misawa, Takashi
|
|
2015
|
23 |
5 |
p. 1055-1061
7 p.
|
artikel
|
| 21 |
Synthesis and biological evaluation of 3-([1,2,4]triazolo[4,3-a]pyridin-3-yl)-4-(indol-3-yl)-maleimides as potent, selective GSK-3β inhibitors and neuroprotective agents
|
Ye, Qing
|
|
2015
|
23 |
5 |
p. 1179-1188
10 p.
|
artikel
|
| 22 |
Synthesis and comparative biological evaluation of bifunctional ligands for radiotherapy applications of 90Y and 177Lu
|
Chong, Hyun-Soon
|
|
2015
|
23 |
5 |
p. 1169-1178
10 p.
|
artikel
|
| 23 |
Synthesis and pharmacological characterization of 2-aminobenzaldehyde oxime analogs as dual inhibitors of neutrophil elastase and proteinase 3
|
Hwang, Tsong-Long
|
|
2015
|
23 |
5 |
p. 1123-1134
12 p.
|
artikel
|
| 24 |
Synthesis and structure–activity relationships of novel phenoxyacetamide inhibitors of the Pseudomonas aeruginosa type III secretion system (T3SS)
|
Williams, John D.
|
|
2015
|
23 |
5 |
p. 1027-1043
17 p.
|
artikel
|
| 25 |
Synthesis, biological evaluation and molecular docking study of novel piperidine and piperazine derivatives as multi-targeted agents to treat Alzheimer’s disease
|
Meena, Poonam
|
|
2015
|
23 |
5 |
p. 1135-1148
14 p.
|
artikel
|
| 26 |
Synthesis of arylpyrazole linked benzimidazole conjugates as potential microtubule disruptors
|
Kamal, Ahmed
|
|
2015
|
23 |
5 |
p. 1082-1095
14 p.
|
artikel
|
| 27 |
Synthesis of (+)-crocacin D and simplified bioactive analogues
|
Pasqua, Adele E.
|
|
2015
|
23 |
5 |
p. 1062-1068
7 p.
|
artikel
|
| 28 |
Synthesis of new ligands for targeting the S1P1 receptor
|
Schilson, Stefanie S.
|
|
2015
|
23 |
5 |
p. 1011-1026
16 p.
|
artikel
|
| 29 |
Synthesis, structure activity relationship, radiolabeling and preclinical evaluation of high affinity ligands for the ion channel of the N-methyl-d-aspartate receptor as potential imaging probes for positron emission tomography
|
Klein, Pieter J.
|
|
2015
|
23 |
5 |
p. 1189-1206
18 p.
|
artikel
|
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