| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
2-Alkyl substituted benzimidazoles as a new class of selective AT2 receptor ligands
|
Roy, Tamal
|
|
|
66 |
C |
p.
|
artikel
|
| 2 |
DeepAS – Chemical language model for the extension of active analogue series
|
Yoshimori, Atsushi
|
|
|
66 |
C |
p.
|
artikel
|
| 3 |
Design and synthesis of unprecedented 9- and 10-membered cyclonucleosides with PRMT5 inhibitory activity
|
Kawamura, Shuhei
|
|
|
66 |
C |
p.
|
artikel
|
| 4 |
Design, synthesis and biological evaluation of novel indole derivatives as gut-selective NaPi2b inhibitors
|
Ushiki, Yasunobu
|
|
|
66 |
C |
p.
|
artikel
|
| 5 |
Design, synthesis and structure–activity relationship of 4-(1,1,1,3,3,3-hexafluoro-2-hydroxyisoprop-2-yl)phenylsilane derivatives as liver X receptor agonists
|
Namba, Nao
|
|
|
66 |
C |
p.
|
artikel
|
| 6 |
Discovery of 2,4-diarylaminopyrimidine derivatives bearing dithiocarbamate moiety as novel ALK inhibitors
|
Wang, Xinyue
|
|
|
66 |
C |
p.
|
artikel
|
| 7 |
Discovery of diarylheptanoids that activate α7 nAchR-JAK2-STAT3 signaling in macrophages with anti-inflammatory activity in vitro and in vivo
|
Lin, Yuan
|
|
|
66 |
C |
p.
|
artikel
|
| 8 |
Discovery of novel benzimidazole derivatives as potent p300 bromodomain inhibitors with anti-proliferative activity in multiple cancer cells
|
Chen, Zonglong
|
|
|
66 |
C |
p.
|
artikel
|
| 9 |
Discovery of novel chloropyramine-cinnamic acid hybrids as potential FAK inhibitors for intervention of metastatic triple-negative breast cancer
|
Yang, Fei
|
|
|
66 |
C |
p.
|
artikel
|
| 10 |
Editorial Board
|
|
|
|
66 |
C |
p.
|
artikel
|
| 11 |
Graphical Abstract Contents Continued
|
|
|
|
66 |
C |
p.
|
artikel
|
| 12 |
Graphical abstract TOC
|
|
|
|
66 |
C |
p.
|
artikel
|
| 13 |
Graphical abstract TOC
|
|
|
|
66 |
C |
p.
|
artikel
|
| 14 |
Hybrids of polyphenolic acids and xanthone, the potential preventive and therapeutic effects on PD: Design, synthesis, in vitro anti-aggregation of α-synuclein, and disaggregation against the existed α-synuclein oligomer and fibril
|
Han, Feng
|
|
|
66 |
C |
p.
|
artikel
|
| 15 |
Identification of benzamides derivatives of norfloxacin as promising microRNA-21 inhibitors via repressing its transcription
|
Xi, Xiao-Xiao
|
|
|
66 |
C |
p.
|
artikel
|
| 16 |
New antimalarials identified by a cell-based phenotypic approach: Structure–activity relationships of 2,3,4,9-tetrahydro-1H-β-carboline derivatives possessing a 2-((coumarin-5-yl)oxy)alkanoyl moiety
|
Cho, Nobuo
|
|
|
66 |
C |
p.
|
artikel
|
| 17 |
On the kinetic mechanism of dimethylarginine dimethylaminohydrolase
|
Johnson, Corey M.
|
|
|
66 |
C |
p.
|
artikel
|
| 18 |
Optimization of ODAP-Urea-based dual-modality PSMA targeting probes for sequential PET-CT and optical imaging
|
Li, Yuan
|
|
|
66 |
C |
p.
|
artikel
|
| 19 |
RNA-templated chemical synthesis of proapoptotic L- and d-peptides
|
Chang, Li-Hao
|
|
|
66 |
C |
p.
|
artikel
|
| 20 |
Silybins are stereospecific regulators of the 20S proteasome
|
Persico, Marco
|
|
|
66 |
C |
p.
|
artikel
|
| 21 |
Synthesis and biological evaluation of novel 2-azido muramyl dipeptide as NOD2 agonistic adjuvants
|
Reddy, Paturu Rama Subba
|
|
|
66 |
C |
p.
|
artikel
|
| 22 |
Synthesis and characterization of an orally bioavailable small molecule agonist of the apelin receptor
|
Narayanan, Sanju
|
|
|
66 |
C |
p.
|
artikel
|
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