| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Contents continued
|
|
|
|
86 |
C |
p.
|
artikel
|
| 2 |
Design and synthesis of thiadiazole-oxadiazole-acetamide derivatives: Elastase inhibition, cytotoxicity, kinetic mechanism, and computational studies
|
Hosseini Nasab, Narges
|
|
|
86 |
C |
p.
|
artikel
|
| 3 |
Design, synthesis, and biological evaluation of acyl sulfonamide derivatives with spiro cycles as NaV1.7 inhibitors for antinociception
|
Ouyang, Xiangshuo
|
|
|
86 |
C |
p.
|
artikel
|
| 4 |
Development of versatile solid-phase methods for syntheses of PROTACs with diverse E3 ligands
|
Xu, Hanqiao
|
|
|
86 |
C |
p.
|
artikel
|
| 5 |
Discovery of 4-oxo-4,5-dihydropyrazolo[1,5-a]quinoxaline-7-carboxamide derivatives as PI3Kα inhibitors via virtual screening and docking-based structure optimization
|
Gu, Dongyan
|
|
|
86 |
C |
p.
|
artikel
|
| 6 |
Dual targeted 2-Benzylideneindanone pendant hydroxamic acid group exhibits selective HDAC6 inhibition along with tubulin stabilization effect
|
Kumar, Kapil
|
|
|
86 |
C |
p.
|
artikel
|
| 7 |
Editorial Board
|
|
|
|
86 |
C |
p.
|
artikel
|
| 8 |
Graphical abstract TOC
|
|
|
|
86 |
C |
p.
|
artikel
|
| 9 |
Graphical abstract TOC
|
|
|
|
86 |
C |
p.
|
artikel
|
| 10 |
New insight into the bioactivity of substituted benzimidazole derivatives: Repurposing from anti-HIV activity to cell migration inhibition targeting hnRNP M
|
Radwan, Mohamed O.
|
|
|
86 |
C |
p.
|
artikel
|
| 11 |
Structure-Activity relationships of replacements for the triazolopyridazine of Anti-Cryptosporidium lead SLU-2633
|
Oboh, Edmund
|
|
|
86 |
C |
p.
|
artikel
|
| 12 |
The aptamer-based RNA-PROTAC
|
Xu, Yan
|
|
|
86 |
C |
p.
|
artikel
|
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