| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
10-Alkoxy-anthracenyl-isoxazole analogs have sub-micromolar activity against a Glioblastoma multiforme cell line
|
Duncan, Nathan S.
|
|
|
69 |
C |
p.
|
artikel
|
| 2 |
2-Aminopyridines with a shortened amino sidechain as potent, selective, and highly permeable human neuronal nitric oxide synthase inhibitors
|
Vasu, Dhananjayan
|
|
|
69 |
C |
p.
|
artikel
|
| 3 |
Berberine and folic acid co-modified pH-sensitive cascade-targeted PTX-liposomes coated with Tween 80 for treating glioma
|
Yang, Chunyan
|
|
|
69 |
C |
p.
|
artikel
|
| 4 |
Bioreducible polyethylenimine core–shell nanostructures as efficient and non-toxic gene and drug delivery vectors
|
Jena, H.
|
|
|
69 |
C |
p.
|
artikel
|
| 5 |
Copper-mediated radioiodination and radiobromination via aryl boronic precursor and its application to 125I/77Br–labeled prostate-specific membrane antigen imaging probes
|
Kondo, Yuto
|
|
|
69 |
C |
p.
|
artikel
|
| 6 |
Corrigendum to “Silybins are stereospecific regulators of the 20S proteasome” [Bioorgan. Med. Chem. 66 (2022) 116813]
|
Persico, Marco
|
|
|
69 |
C |
p.
|
artikel
|
| 7 |
Design, synthesis, and bioactivity study on Lissodendrins B derivatives as PARP1 inhibitor
|
Liu, Xinning
|
|
|
69 |
C |
p.
|
artikel
|
| 8 |
Design, synthesis, and biological evaluation of a new series of pyrazole derivatives: Discovery of potent and selective JNK3 kinase inhibitors
|
Abu Rabah, Reinad R.
|
|
|
69 |
C |
p.
|
artikel
|
| 9 |
Design, synthesis and evaluation of alpha lipoic acid derivatives to treat multiple sclerosis-associated central neuropathic pain
|
Kong, Dehui
|
|
|
69 |
C |
p.
|
artikel
|
| 10 |
Discovery of potent dual ligands for dopamine D4 and σ1 receptors
|
Levoin, Nicolas
|
|
|
69 |
C |
p.
|
artikel
|
| 11 |
Editorial Board
|
|
|
|
69 |
C |
p.
|
artikel
|
| 12 |
Efficient delivery of PKN3 shRNA for the treatment of breast cancer via lipid nanoparticles
|
Liu, Chao
|
|
|
69 |
C |
p.
|
artikel
|
| 13 |
Evaluation of crotamine based probes as intracellular targeted contrast agents for magnetic resonance imaging
|
Joshi, Rajendra
|
|
|
69 |
C |
p.
|
artikel
|
| 14 |
Fragment hopping protocol for the design of small-molecule protein–protein interaction inhibitors
|
Kell, Shelby R.
|
|
|
69 |
C |
p.
|
artikel
|
| 15 |
Graphical Abstract Contents Continued
|
|
|
|
69 |
C |
p.
|
artikel
|
| 16 |
Graphical abstract TOC
|
|
|
|
69 |
C |
p.
|
artikel
|
| 17 |
Graphical abstract TOC
|
|
|
|
69 |
C |
p.
|
artikel
|
| 18 |
Improving the solubility and antileukemia activity of Wnt/β-catenin signaling inhibitors by disrupting molecular planarity
|
Ai, Yong
|
|
|
69 |
C |
p.
|
artikel
|
| 19 |
Junctions in DNA: underexplored targets for therapeutic intervention
|
Ivens, Eleanor
|
|
|
69 |
C |
p.
|
artikel
|
| 20 |
MicroRNA detection in biologically relevant media using a split aptamer platform
|
Wang, Liming
|
|
|
69 |
C |
p.
|
artikel
|
| 21 |
More than forty years of nucleic acid structural science
|
Parkinson, Gary N.
|
|
|
69 |
C |
p.
|
artikel
|
| 22 |
pH-responsive Mannose-modified ferrocene Metal-Organic frameworks with rare earth for Tumor-targeted synchronous Chemo/Chemodynamic therapy
|
Dong, Junliang
|
|
|
69 |
C |
p.
|
artikel
|
| 23 |
Recent advances on synthesis and biological activities of C-17 aza-heterocycle derived steroids
|
Huo, Haibo
|
|
|
69 |
C |
p.
|
artikel
|
| 24 |
SPION nanoparticles for delivery of dopaminergic isoquinoline and benzazepine derivatives
|
Lucena-Serrano, Cristina
|
|
|
69 |
C |
p.
|
artikel
|
| 25 |
Structure-activity relationships of 2-pyrimidinecarbohydrazides as utrophin modulators for the potential treatment of Duchenne muscular dystrophy
|
Chatzopoulou, Maria
|
|
|
69 |
C |
p.
|
artikel
|
| 26 |
Synthesis and biological evaluation of a tumor-selective degrader of PARP1
|
Pu, Chunlan
|
|
|
69 |
C |
p.
|
artikel
|
| 27 |
Synthesis and biological evaluation of 4H-benzo[e][1,3]oxazin-4-ones analogues of TGX-221 as inhibitors of PI3Kβ
|
Mohammed, Ehtesham U.R.
|
|
|
69 |
C |
p.
|
artikel
|
| 28 |
Synthesis and biological evaluation of hybrids from optically active ring-opened 3-N-butylphthalide derivatives and 4-fluro-edaravone as potential anti-acute ischemic stroke agents
|
Jia, Jian
|
|
|
69 |
C |
p.
|
artikel
|
| 29 |
Synthesis and evaluation of inhibitors of Mycobacterium tuberculosis UGM using bioisosteric replacement
|
Fu, Jian
|
|
|
69 |
C |
p.
|
artikel
|
| 30 |
The protective effects of natural product tunicatachalcone against neuroinflammation via targeting RIPK2 in microglia BV-2 cells stimulated by LPS
|
Wen, Ran
|
|
|
69 |
C |
p.
|
artikel
|
| 31 |
Withaferin A, a polyfunctional pharmacophore that includes covalent engagement of IPO5, is an inhibitor of influenza A replication
|
Patouret, Remi
|
|
|
69 |
C |
p.
|
artikel
|
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