| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Application of marine natural products in drug research
|
Lu, Wen-Yu
|
|
|
35 |
C |
p.
|
artikel
|
| 2 |
Design and synthesis of a monocyclic derivative as a selective ACC1 inhibitor by chemical modification of biphenyl ACC1/2 dual inhibitors
|
Mizojiri, Ryo
|
|
|
35 |
C |
p.
|
artikel
|
| 3 |
Discovery of a potent G-protein-coupled receptor 119 agonist for the treatment of type 2 diabetes
|
Pola, Suresh
|
|
|
35 |
C |
p.
|
artikel
|
| 4 |
Editorial Board
|
|
|
|
35 |
C |
p.
|
artikel
|
| 5 |
Graphical Abstract Contents Continued
|
|
|
|
35 |
C |
p.
|
artikel
|
| 6 |
Graphical abstract TOC
|
|
|
|
35 |
C |
p.
|
artikel
|
| 7 |
Graphical abstract TOC
|
|
|
|
35 |
C |
p.
|
artikel
|
| 8 |
Loop-mediated fluorescent probes for selective discrimination of parallel and antiparallel G-Quadruplexes
|
Pandith, Anup
|
|
|
35 |
C |
p.
|
artikel
|
| 9 |
Manganese(III) porphyrin oligomers as high-relaxivity MRI contrast agents
|
Lu, Hui-Shan
|
|
|
35 |
C |
p.
|
artikel
|
| 10 |
Novel 3-benzylidene/benzylphthalide Mannich base derivatives as potential multifunctional agents for the treatment of Alzheimer’s disease
|
Cao, Zhongcheng
|
|
|
35 |
C |
p.
|
artikel
|
| 11 |
Potential of substituted quinazolines to interact with multiple targets in the treatment of cancer
|
Choudhary, Shruti
|
|
|
35 |
C |
p.
|
artikel
|
| 12 |
Retro-aza-Michael reaction of an o-aminophenol adduct in protic solvents inspired by natural products
|
Takenaka, Kei
|
|
|
35 |
C |
p.
|
artikel
|
| 13 |
Small molecule inhibitor E-64 exhibiting the activity against African swine fever virus pS273R
|
Liu, Bangzuo
|
|
|
35 |
C |
p.
|
artikel
|
| 14 |
Streptochlorin analogues as potential antifungal agents: Design, synthesis, antifungal activity and molecular docking study
|
Gao, Ya
|
|
|
35 |
C |
p.
|
artikel
|
| 15 |
Structure-activity relationship and mechanistic studies for a series of cinnamyl hydroxamate histone deacetylase inhibitors
|
Tavares, Maurício Temotheo
|
|
|
35 |
C |
p.
|
artikel
|
| 16 |
Structure-based designing and synthesis of 2-phenylchromone derivatives as potent tyrosinase inhibitors: In vitro and in silico studies
|
Ashraf, Jamshaid
|
|
|
35 |
C |
p.
|
artikel
|
| 17 |
Synthesis and biological activity of selenopsammaplin A and its analogues as antitumor agents with DOT1L inhibitory activity
|
Ju Han, Hae
|
|
|
35 |
C |
p.
|
artikel
|
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