| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel GSK-3 inhibitor binds to GSK-3β via a reversible, time and Cys-199-dependent mechanism
|
Ghazanfari, Davoud
|
|
|
40 |
C |
p.
|
artikel
|
| 2 |
Corrigendum to ‘Design and synthesis of Coenzyme A analogues as Aurora kinase A inhibitors: An exploration of the roles of the pyrophosphate and pantetheine moieties’. [Bioorg. Med. Chem. 28 (2020) 115740]
|
Bellany, Fiona
|
|
|
40 |
C |
p.
|
artikel
|
| 3 |
Design and synthesis of garlic-related unsymmetrical thiosulfonates as potential Alzheimer’s disease therapeutics: In vitro and in silico study
|
Zilbeyaz, Kani
|
|
|
40 |
C |
p.
|
artikel
|
| 4 |
Design, synthesis and anti-HIV evaluation of novel 5-substituted diarylpyrimidine derivatives as potent HIV-1 NNRTIs
|
Gao, Ping
|
|
|
40 |
C |
p.
|
artikel
|
| 5 |
Design, synthesis and biological evaluation of imidazopyridazine derivatives containing isoquinoline group as potent MNK1/2 inhibitors
|
Bu, Hong
|
|
|
40 |
C |
p.
|
artikel
|
| 6 |
Design, synthesis, and biological evaluation of stapled ascaphin-8 peptides
|
Liu, Jing
|
|
|
40 |
C |
p.
|
artikel
|
| 7 |
Design, synthesis and lipid-lowering activities of penipyridone derivatives
|
Li, Liping
|
|
|
40 |
C |
p.
|
artikel
|
| 8 |
Discovery of novel tripeptide propylene oxide proteasome inhibitors for the treatment of multiple myeloma
|
Zhang, Wen
|
|
|
40 |
C |
p.
|
artikel
|
| 9 |
Discovery of potent and selective reversible Bruton’s tyrosine kinase inhibitors
|
Qiu, Hui
|
|
|
40 |
C |
p.
|
artikel
|
| 10 |
Discovery of pyrazolones as novel carboxylesterase 2 inhibitors that potently inhibit the adipogenesis in cells
|
Qian, Xing-Kai
|
|
|
40 |
C |
p.
|
artikel
|
| 11 |
Editorial Board
|
|
|
|
40 |
C |
p.
|
artikel
|
| 12 |
Exploiting the HSP60/10 chaperonin system as a chemotherapeutic target for colorectal cancer
|
Ray, Anne-Marie
|
|
|
40 |
C |
p.
|
artikel
|
| 13 |
Fused chromeno and quinolino[1,8]naphthyridines: Synthesis and biological evaluation as topoisomerase I inhibitors and antiproliferative agents
|
Martín-Encinas, Endika
|
|
|
40 |
C |
p.
|
artikel
|
| 14 |
Graphical Abstract Contents Continued
|
|
|
|
40 |
C |
p.
|
artikel
|
| 15 |
Graphical abstract TOC
|
|
|
|
40 |
C |
p.
|
artikel
|
| 16 |
Graphical abstract TOC
|
|
|
|
40 |
C |
p.
|
artikel
|
| 17 |
Normalization of DNA encoded library affinity selection results driven by high throughput sequencing and HPLC purification
|
Rama-Garda, Ramón
|
|
|
40 |
C |
p.
|
artikel
|
| 18 |
Novel hybrid conjugates with dual estrogen receptor α degradation and histone deacetylase inhibitory activities for breast cancer therapy
|
Zhao, Chenxi
|
|
|
40 |
C |
p.
|
artikel
|
| 19 |
Novel 4-(piperazin-1-yl)quinolin-2(1H)-one bearing thiazoles with antiproliferative activity through VEGFR-2-TK inhibition
|
Hassan, Abdelfattah
|
|
|
40 |
C |
p.
|
artikel
|
| 20 |
Probing cytochrome P450 (CYP) bioactivation with chloromethylindoline bioprecursors derived from the duocarmycin family of compounds
|
Ortuzar, Natalia
|
|
|
40 |
C |
p.
|
artikel
|
| 21 |
Proposal for the binding mode of the 23-mer inhibitory peptide to myostatin
|
Asari, Tomo
|
|
|
40 |
C |
p.
|
artikel
|
| 22 |
Ruthenium(II)- and Palladium(II)-catalyzed position-divergent CH oxygenations of arylated quinones: Identification of hydroxylated quinonoid compounds with potent trypanocidal activity
|
Gontijo, Talita B.
|
|
|
40 |
C |
p.
|
artikel
|
| 23 |
Spectroscopic and biochemical characterization of metallo-β-lactamase IMP-1 with dicarboxylic, sulfonyl, and thiol inhibitors
|
Zhang, Huan
|
|
|
40 |
C |
p.
|
artikel
|
| 24 |
Synthesis of osthol-based botanical fungicides and their antifungal application in crop protection
|
Guo, Yuying
|
|
|
40 |
C |
p.
|
artikel
|
| 25 |
The chemistry and biology of phosphatidylinositol 4-phosphate at the plasma membrane
|
Batrouni, Alex G.
|
|
|
40 |
C |
p.
|
artikel
|
| 26 |
The DNA binding properties of 9-aminoacridine carboxamide Pt complexes
|
Kava, Hieronimus W.
|
|
|
40 |
C |
p.
|
artikel
|
Tijdschrift beschrijving