nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
5-Adamantan thiadiazole-based thiazolidinones as antimicrobial agents. Design, synthesis, molecular docking and evaluation
|
Fesatidou, Maria |
|
|
26 |
16 |
p. 4664-4676 |
artikel |
2 |
A latent green fluorescent styrylcoumarin probe for the selective growth and detection of Gram negative bacteria
|
Váradi, Linda |
|
|
26 |
16 |
p. 4745-4750 |
artikel |
3 |
Antiprotozoal and cysteine proteases inhibitory activity of dipeptidyl enoates
|
Royo, Santiago |
|
|
26 |
16 |
p. 4624-4634 |
artikel |
4 |
A series of camptothecin prodrugs exhibit HDAC inhibition activity
|
Zhu, Qiwen |
|
|
26 |
16 |
p. 4706-4715 |
artikel |
5 |
Characterization of crystal water molecules in a high-affinity inhibitor and hematopoietic prostaglandin D synthase complex by interaction energy studies
|
Takaya, Daisuke |
|
|
26 |
16 |
p. 4726-4734 |
artikel |
6 |
Decoy peptides derived from the extracellular domain of toll-like receptor 2 (TLR2) show anti-inflammatory properties
|
Ebner, S. |
|
|
26 |
16 |
p. 4615-4623 |
artikel |
7 |
Design and synthesis of novel 6-hydroxy-4-methoxy-3-methylbenzofuran-7-carboxamide derivatives as potent Mnks inhibitors by fragment-based drug design
|
Wang, Shuxiang |
|
|
26 |
16 |
p. 4602-4614 |
artikel |
8 |
Design, synthesis and structure-activity relationship of diaryl-ureas with novel isoxazol[3,4-b]pyridine-3-amino-structure as multi-target inhibitors against receptor tyrosine kinase
|
Shi, Zhi-Hao |
|
|
26 |
16 |
p. 4735-4744 |
artikel |
9 |
Dual-targeting for brain-specific liposomes drug delivery system: Synthesis and preliminary evaluation
|
Peng, Yao |
|
|
26 |
16 |
p. 4677-4686 |
artikel |
10 |
Editorial Board
|
|
|
|
26 |
16 |
p. ii |
artikel |
11 |
Graphical abstract TOC
|
|
|
|
26 |
16 |
p. IBC |
artikel |
12 |
Graphical abstract TOC
|
|
|
|
26 |
16 |
p. I-III |
artikel |
13 |
Graphical abstract TOC
|
|
|
|
26 |
16 |
p. OBC |
artikel |
14 |
Gymnotic delivery and gene silencing activity of reduction-responsive siRNAs bearing lipophilic disulfide-containing modifications at 2′-position
|
Gauthier, Florian |
|
|
26 |
16 |
p. 4635-4643 |
artikel |
15 |
In vitro and in vivo pharmacokinetic and pharmacodynamic study of MBRI-001, a deuterium-substituted plinabulin derivative as a potent anti-cancer agent
|
Ma, Mingxu |
|
|
26 |
16 |
p. 4687-4692 |
artikel |
16 |
Optimization of diarylpentadienones as chemotherapeutics for prostate cancer
|
Patanapongpibul, Manee |
|
|
26 |
16 |
p. 4751-4760 |
artikel |
17 |
Phosphorescent ruthenium complexes with bromopyrene unit that enhance oxygen sensitivity
|
Kurihara, Ryohsuke |
|
|
26 |
16 |
p. 4595-4601 |
artikel |
18 |
Radiosynthesis and in vivo evaluation of a fluorine-18 labeled pyrazine based radioligand for PET imaging of the adenosine A2B receptor
|
Lindemann, Marcel |
|
|
26 |
16 |
p. 4650-4663 |
artikel |
19 |
Synthesis and bioactivities evaluation of l-pyroglutamic acid analogues from natural product lead
|
Gang, Fang-li |
|
|
26 |
16 |
p. 4644-4649 |
artikel |
20 |
Synthesis and evaluation of 1,2,3,4-tetrahydro-1-acridone analogues as potential dual inhibitors for amyloid-beta and tau aggregation
|
Lv, Peng |
|
|
26 |
16 |
p. 4693-4705 |
artikel |
21 |
Synthesis, molecular docking, and biological activity of 2-vinyl chromones: Toward selective butyrylcholinesterase inhibitors for potential Alzheimer's disease therapeutics
|
Makhaeva, Galina F. |
|
|
26 |
16 |
p. 4716-4725 |
artikel |