nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
4-Arylidene curcumin derivatives in vitro inhibit α-Synuclein aggregation and disaggregate the preformed fibril
|
Liu, Wei |
|
|
96 |
C |
p. |
artikel |
2 |
Beyond traditional methods: Unveiling the skin whitening properties of Rhein-Embedded PROTACs
|
Xu, Meng |
|
|
96 |
C |
p. |
artikel |
3 |
Biocompatible conjugated polymer nanoparticles labeled with 225Ac for tumor endoradiotherapy
|
Chen, Xijian |
|
|
96 |
C |
p. |
artikel |
4 |
Contents continued
|
|
|
|
96 |
C |
p. |
artikel |
5 |
Design, synthesis, and biological evaluation of deuterated indolepropionic acid derivatives as novel long-acting pan PPARα/γ/δ agonists
|
Chen, Lianru |
|
|
96 |
C |
p. |
artikel |
6 |
Design, synthesis and biological evaluation of EGFR kinase inhibitors that spans the orthosteric and allosteric sites
|
Fan, Mengmeng |
|
|
96 |
C |
p. |
artikel |
7 |
Development of 3-acetylindole derivatives that selectively target BRPF1 as new inhibitors of receptor activator of NF-κB ligand (RANKL)-Induced osteoclastogenesis
|
Zhang, Wenqiang |
|
|
96 |
C |
p. |
artikel |
8 |
Development of novel quinoline-NO donor hybrids inducing human breast cancer cells apoptosis via inhibition of topoisomerase I
|
Wu, Guiying |
|
|
96 |
C |
p. |
artikel |
9 |
Discovery of a new dihydroeugenol-chalcone hybrid with cytotoxic and anti-migratory potential: A dual-action hit for cancer therapeutics
|
Nakao, Izadora Amaral |
|
|
96 |
C |
p. |
artikel |
10 |
Discovery of a novel GPR35 agonist with high and equipotent species potency for oral treatment of IBD
|
Song, Zhaoxiang |
|
|
96 |
C |
p. |
artikel |
11 |
Discovery of conformationally constrained c-Abl inhibitors with potential neuroprotective effects against Parkinson’s disease
|
Yang, Zichao |
|
|
96 |
C |
p. |
artikel |
12 |
Discovery of novel dual Bruton’s tyrosine kinase (BTK) and Janus kinase 3 (JAK3) inhibitors as a promising strategy for rheumatoid arthritis
|
Liang, Tingting |
|
|
96 |
C |
p. |
artikel |
13 |
Editorial Board
|
|
|
|
96 |
C |
p. |
artikel |
14 |
Glutathione-responsive PROTAC for targeted degradation of ERα in breast cancer cells
|
Zhou, Zhili |
|
|
96 |
C |
p. |
artikel |
15 |
Graphical abstract TOC
|
|
|
|
96 |
C |
p. |
artikel |
16 |
Graphical abstract TOC
|
|
|
|
96 |
C |
p. |
artikel |
17 |
Harvesting phosphorus-containing moieties for their antibacterial effects
|
Voráčová, Manuela |
|
|
96 |
C |
p. |
artikel |
18 |
Hesperidin Methyl Chalcone reduces extracellular Aβ(25-35) peptide aggregation and fibrillation and also protects Neuro 2a cells from Aβ(25-35) induced neuronal dysfunction
|
Jafni, Sakthivel |
|
|
96 |
C |
p. |
artikel |
19 |
Identification of Ebselen derivatives as novel SARS-CoV-2 main protease inhibitors: Design, synthesis, biological evaluation, and structure-activity relationships exploration
|
Zhang, Heng |
|
|
96 |
C |
p. |
artikel |
20 |
In situ click chemistry-based discovery of 1,2,3-triazole-derived diarylpyrimidines as novel HIV-1 NNRTIs by exploiting the tolerant region I in binding pocket
|
Sun, Yanying |
|
|
96 |
C |
p. |
artikel |
21 |
Multifunctional agents against Alzheimer’s disease based on oxidative stress: Polysubstituted pyrazine derivatives synthesized by multicomponent reactions
|
Wei, Wenxiu |
|
|
96 |
C |
p. |
artikel |
22 |
New aryl-/heteroarylpiperazine derivatives of 1,7-dimethyl-8,9-diphenyl-4-azatricyclo[5.2.1.02,6]dec-8-ene-3,5,10-trione: Synthesis and preliminary studies of biological activities
|
Napiórkowska, Mariola |
|
|
96 |
C |
p. |
artikel |
23 |
Review and prospects of targeted therapies for Spleen tyrosine kinase (SYK)
|
Wang, Zhaozhao |
|
|
96 |
C |
p. |
artikel |
24 |
Structure-guided design and synthesis of ATP-competitive N-acyl-substituted sulfamide d-alanine-d-alanine ligase inhibitors
|
Becker, Rouven |
|
|
96 |
C |
p. |
artikel |
25 |
Target discovery of bioactive natural products with native-compound-coupled CNBr-activated Sepharose 4B beads (NCCB): Applications, mechanisms and outlooks
|
Zhang, Yueteng |
|
|
96 |
C |
p. |
artikel |