| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Anti-inflammatory drimane sesquiterpene lactones from an Aspergillus species
|
Felix, Silke
|
|
2014
|
22 |
11 |
p. 2912-2918
7 p.
|
artikel
|
| 2 |
A rational design strategy of the novel topoisomerase II inhibitors for the synthesis of the 4-O-(2-pyrazinecarboxylic)-4′-demethylepipodophyllotoxin with antitumor activity by diminishing the relaxation reaction of topoisomerase II-DNA decatenation
|
Zhao, Wei
|
|
2014
|
22 |
11 |
p. 2998-3007
10 p.
|
artikel
|
| 3 |
Bis(4-hydroxy-2H-chromen-2-one): Synthesis and effects on leukemic cell lines proliferation and NF-κB regulation
|
Talhi, Oualid
|
|
2014
|
22 |
11 |
p. 3008-3015
8 p.
|
artikel
|
| 4 |
Corrigendum to “Discovery of a new 2-aminobenzhydrol template for highly potent squalene synthase inhibitors” [Bioorg. Med. Chem. 19 (2011) 1930–1949]
|
Ichikawa, Masanori
|
|
2014
|
22 |
11 |
p. 3065-
1 p.
|
artikel
|
| 5 |
Design, synthesis and biological evaluation of novel tripeptidyl epoxyketone derivatives constructed from β-amino acid as proteasome inhibitors
|
Zhang, Jiankang
|
|
2014
|
22 |
11 |
p. 2955-2965
11 p.
|
artikel
|
| 6 |
Design, synthesis and preliminary evaluation of α-sulfonyl γ-(glycinyl-amino)proline peptidomimetics as matrix metalloproteinase inhibitors
|
Zhang, Jian
|
|
2014
|
22 |
11 |
p. 3055-3064
10 p.
|
artikel
|
| 7 |
Development of caged non-hydrolyzable phosphoamino acids and application to photo-control of binding affinity of phosphopeptide mimetic to phosphopeptide-recognizing protein
|
Ebisuno, Koji
|
|
2014
|
22 |
11 |
p. 2984-2991
8 p.
|
artikel
|
| 8 |
Editorial board
|
|
|
2014
|
22 |
11 |
p. IFC-
1 p.
|
artikel
|
| 9 |
Effect of each guanidinium group on the RNA recognition and cellular uptake of Tat-derived peptides
|
Wu, Cheng-Hsun
|
|
2014
|
22 |
11 |
p. 3016-3020
5 p.
|
artikel
|
| 10 |
From norbornane-based nucleotide analogs locked in South conformation to novel inhibitors of feline herpes virus
|
Dejmek, Milan
|
|
2014
|
22 |
11 |
p. 2974-2983
10 p.
|
artikel
|
| 11 |
Graphical contents list
|
|
|
2014
|
22 |
11 |
p. 2907-2911
5 p.
|
artikel
|
| 12 |
Identification of trisubstituted-pyrazol carboxamide analogs as novel and potent antagonists of farnesoid X receptor
|
Yu, Donna D.
|
|
2014
|
22 |
11 |
p. 2919-2938
20 p.
|
artikel
|
| 13 |
Identifying structural determinants of potency for analogs of apelin-13: Integration of C-terminal truncation with structure–activity
|
Zhang, Yanyan
|
|
2014
|
22 |
11 |
p. 2992-2997
6 p.
|
artikel
|
| 14 |
Structure–activity relationships and colorimetric properties of specific probes for the putative cancer biomarker human arylamine N-acetyltransferase 1
|
Egleton, James E.
|
|
2014
|
22 |
11 |
p. 3030-3054
25 p.
|
artikel
|
| 15 |
Structure–activity relationship study, target identification, and pharmacological characterization of a small molecular IL-12/23 inhibitor, APY0201
|
Hayakawa, Nobuhiko
|
|
2014
|
22 |
11 |
p. 3021-3029
9 p.
|
artikel
|
| 16 |
Sulfonamide inhibition studies of two β-carbonic anhydrases from the bacterial pathogen Legionella pneumophila
|
Nishimori, Isao
|
|
2014
|
22 |
11 |
p. 2939-2946
8 p.
|
artikel
|
| 17 |
Synthesis and evaluation of immunostimulant plasmalogen lysophosphatidylethanolamine and analogues for natural killer T cells
|
Ni, Guanghui
|
|
2014
|
22 |
11 |
p. 2966-2973
8 p.
|
artikel
|
| 18 |
Synthesis, biological evaluation, and molecular docking studies of novel 2-styryl-5-nitroimidazole derivatives containing 1,4-benzodioxan moiety as FAK inhibitors with anticancer activity
|
Duan, Yong-Tao
|
|
2014
|
22 |
11 |
p. 2947-2954
8 p.
|
artikel
|
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