| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A turn for the worse: Aβ β-hairpins in Alzheimer’s disease
|
Ruttenberg, Sarah M.
|
|
|
105 |
C |
p.
|
artikel
|
| 2 |
Contents continued
|
|
|
|
105 |
C |
p.
|
artikel
|
| 3 |
Design, synthesis, and evaluation of formylpiperazine analogs of Ferrostatin-1 as novel improved ferroptosis inhibitors
|
Ji, Hua-Long
|
|
|
105 |
C |
p.
|
artikel
|
| 4 |
Discovery of harmiprims, harmine-primaquine hybrids, as potent and selective anticancer and antimalarial compounds
|
Pavić, Kristina
|
|
|
105 |
C |
p.
|
artikel
|
| 5 |
Discovery of novel pyridone-benzamide derivatives possessing a 1-methyl-2-benzimidazolinone moiety as potent EZH2 inhibitors for the treatment of B-cell lymphomas
|
Wu, Di
|
|
|
105 |
C |
p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
|
105 |
C |
p.
|
artikel
|
| 7 |
Expanding the ligand spaces for E3 ligases for the design of protein degraders
|
Shah Zaib Saleem, Rahman
|
|
|
105 |
C |
p.
|
artikel
|
| 8 |
Graphical abstract TOC
|
|
|
|
105 |
C |
p.
|
artikel
|
| 9 |
Graphical abstract TOC
|
|
|
|
105 |
C |
p.
|
artikel
|
| 10 |
M1/M4 receptors as potential therapeutic treatments for schizophrenia: A comprehensive study
|
Fu, Lingsheng
|
|
|
105 |
C |
p.
|
artikel
|
| 11 |
Molecular basis of N-glycan recognition by pradimicin a and its potential as a SARS-CoV-2 entry inhibitor
|
Nakagawa, Yu
|
|
|
105 |
C |
p.
|
artikel
|
| 12 |
Optimization of benzenesulfonyl derivatives as anti-Trypanosomatidae agents: Structural design, synthesis, and pharmacological assessment against Trypanosoma cruzi and Leishmania infantum
|
Freitas de Lima Hercos, Guilherme
|
|
|
105 |
C |
p.
|
artikel
|
| 13 |
Photodynamic anticancer activity evaluation of novel 5-aminolevulinic acid and 3-hydroxypyridinone conjugates
|
Zhang, Jingqi
|
|
|
105 |
C |
p.
|
artikel
|
| 14 |
Synthesis and biological evaluation of EGFR binding peptides for near-infrared photoimmunotherapy
|
Otani, Takuya
|
|
|
105 |
C |
p.
|
artikel
|
| 15 |
1,2,3-Triazole-totarol conjugates as potent PIP5K1α lipid kinase inhibitors
|
Haidar, Samer
|
|
|
105 |
C |
p.
|
artikel
|
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