nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
An approach for the intracellular delivery of IgG via enzymatic ligation with a cell-permeable attenuated cationic amphiphilic lytic peptide
|
Kawaguchi, Yoshimasa |
|
|
111 |
C |
p. |
artikel |
2 |
An N-terminal heptad repeat trimer-based peptide fusion inhibitor exhibits potent anti-H1N1 activity
|
Na, Heiya |
|
|
111 |
C |
p. |
artikel |
3 |
Contents Continued
|
|
|
|
111 |
C |
p. |
artikel |
4 |
Corrigendum to “Discovery of novel Quinazoline-based KRAS G12C inhibitors as potential anticancer agents” [Bioorg. Med. Chem. 71 (2022) 116962]
|
Li, Ling |
|
|
111 |
C |
p. |
artikel |
5 |
Current status of the small molecule anti-HIV drugs in the pipeline or recently approved
|
Umumararungu, Théoneste |
|
|
111 |
C |
p. |
artikel |
6 |
Design and synthesis of TH19P01-Camptothecin based hybrid peptides inducing effective anticancer responses on sortilin positive cancer cells
|
Li, Ya-Jie |
|
|
111 |
C |
p. |
artikel |
7 |
Design and synthesis of visible light-activatable photocaged peroxides for optical control of ROS-mediated cellular signaling
|
Tsuji, Mieko |
|
|
111 |
C |
p. |
artikel |
8 |
Design, synthesis and biological evaluation of naphthyl amide derivatives as reversible monoacylglycerol lipase (MAGL) inhibitors
|
Yu, Quanwei |
|
|
111 |
C |
p. |
artikel |
9 |
Design, synthesis, and biological evaluation of novel 1-amido-2-one-4-thio-deoxypyranose as potential antitumor agents for multiple myeloma
|
Li, Xiaomei |
|
|
111 |
C |
p. |
artikel |
10 |
Design, synthesis, anti-tumor activity and mechanism of novel PROTACs as degraders of PD-L1 and inhibitors of PD-1/PD-L1 interaction
|
Zhang, Feng |
|
|
111 |
C |
p. |
artikel |
11 |
Development of a high quantum yield probe for detection of mitochondrial G-quadruplexes in live cells based on fluorescence lifetime imaging microscopy
|
Chen, Kai-Yi |
|
|
111 |
C |
p. |
artikel |
12 |
Discovery of a potent, selective, and orally available EGFR C797S mutant inhibitor (DS06652923) with in vivo antitumor activity
|
Kageji, Hideaki |
|
|
111 |
C |
p. |
artikel |
13 |
Discovery of macrocyclic covalent inhibitors for severe acute respiratory syndrome coronavirus 2 3CL protease
|
Tang, Xiubo |
|
|
111 |
C |
p. |
artikel |
14 |
Dual-modified penetratin peptides: Enhancing nucleic acid delivery through stapling and endosomal escape domain
|
Horikoshi, Kanako |
|
|
111 |
C |
p. |
artikel |
15 |
Editorial Board
|
|
|
|
111 |
C |
p. |
artikel |
16 |
FDA-approved small molecule kinase inhibitors for cancer treatment (2001–2015): Medical indication, structural optimization, and binding mode Part I
|
Wang, Ying |
|
|
111 |
C |
p. |
artikel |
17 |
Graphical abstract TOC
|
|
|
|
111 |
C |
p. |
artikel |
18 |
Graphical abstract TOC
|
|
|
|
111 |
C |
p. |
artikel |
19 |
New substituted benzoxazine derivatives as potent inducers of membrane permeability and cell death
|
Conejo-García, Ana |
|
|
111 |
C |
p. |
artikel |
20 |
Novel bibenzyl compound Ae exhibits anti-agiogenic activity in HUVECs in vitro and zebrafish in vivo
|
Guan, Li |
|
|
111 |
C |
p. |
artikel |
21 |
Recent contributions of pyridazine as a privileged scaffold of anticancer agents in medicinal chemistry: An updated review
|
Liu, Zi-Qiang |
|
|
111 |
C |
p. |
artikel |
22 |
Regulation of exercise ability and glycolipid metabolism by synthetic SR9009 analogues as new REV-ERB-α agonists
|
Li, Lei |
|
|
111 |
C |
p. |
artikel |
23 |
RNA modifications identification based on chemical reactions
|
Zhao, Zhengjia |
|
|
111 |
C |
p. |
artikel |
24 |
Synthesis and antiproliferative activity of (−)-cleistenolide, (6S)-cleistenolide and 4-substituted cleistenolide analogues
|
Benedeković, Goran |
|
|
111 |
C |
p. |
artikel |
25 |
Synthesis and biological studies of 2-aminothiophene derivatives as positive allosteric modulators of glucagon-like peptide 1 receptor
|
Campbell, Jeffrey A. |
|
|
111 |
C |
p. |
artikel |
26 |
3-Tetrazolyl-β-carboline derivatives as potential neuroprotective agents
|
Ribeiro, João L.P. |
|
|
111 |
C |
p. |
artikel |
27 |
The selective chemical modification of the 6-amino group of adenosine of the premature termination codon induces readthrough to produce full-length peptide in the reconstituted E. Coli translation system
|
Murase, Hirotaka |
|
|
111 |
C |
p. |
artikel |