| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A new selective inhibitor for IMP-1 metallo-β-lactamase, 3Z,5E-octa-3,5-diene-1,3,4-tricarboxylic acid-3,4-anhydride
|
Ikeda, Akari
|
|
|
78 |
C |
p.
|
artikel
|
| 2 |
Bivalent dopamine agonists with co-operative binding and functional activities at dopamine D2 receptors, modulate aggregation and toxicity of alpha synuclein protein
|
Dinda, Bidyut
|
|
|
78 |
C |
p.
|
artikel
|
| 3 |
Corrigendum to “A novel survivin dimerization inhibitor without a labile hydrazone linker induces spontaneous apoptosis and synergizes with docetaxel in prostate cancer cells” [Bioorg. Med. Chem. 65 (2022) 116761]
|
Peery, Robert
|
|
|
78 |
C |
p.
|
artikel
|
| 4 |
Design, synthesis and antitumor activity of novel thiophene- triazine derivatives bearing arylurea unit as potent PI3K/mTOR inhibitorss
|
Xu, Shan
|
|
|
78 |
C |
p.
|
artikel
|
| 5 |
Design, synthesis, and biological evaluation of BRD4 degraders
|
Ding, Mengyuan
|
|
|
78 |
C |
p.
|
artikel
|
| 6 |
Design, synthesis and biological evaluation of KRASG12C-PROTACs
|
Zhang, Xiaoyi
|
|
|
78 |
C |
p.
|
artikel
|
| 7 |
Design, synthesis, and biological evaluation of quinoxalinone derivatives as potent BRD4 inhibitors
|
Xu, Kai-Yan
|
|
|
78 |
C |
p.
|
artikel
|
| 8 |
Development of a spermine lipid for transient antibody expression
|
Sui, Shaowei
|
|
|
78 |
C |
p.
|
artikel
|
| 9 |
Discovery and characterization of orally bioavailable 4-chloro-6-fluoroisophthalamides as covalent PPARG inverse-agonists
|
Orsi, Douglas L.
|
|
|
78 |
C |
p.
|
artikel
|
| 10 |
Dual functional antioxidant and butyrylcholinesterase inhibitors for the treatment of Alzheimer’s disease: Design, synthesis and evaluation of novel melatonin-alkylbenzylamine hybrids
|
Liu, Peng
|
|
|
78 |
C |
p.
|
artikel
|
| 11 |
Editorial Board
|
|
|
|
78 |
C |
p.
|
artikel
|
| 12 |
Efficient delivery of VEGFA mRNA for promoting wound healing via ionizable lipid nanoparticles
|
Dong, Shuo
|
|
|
78 |
C |
p.
|
artikel
|
| 13 |
Fine-tuning of nitrogen-containing bisphosphonate esters that potently induce degradation of HMG-CoA reductase
|
Kawamura, Kota
|
|
|
78 |
C |
p.
|
artikel
|
| 14 |
Graphical abstract TOC
|
|
|
|
78 |
C |
p.
|
artikel
|
| 15 |
Graphical abstract TOC
|
|
|
|
78 |
C |
p.
|
artikel
|
| 16 |
Graphical abstract TOC
|
|
|
|
78 |
C |
p.
|
artikel
|
| 17 |
Harnessing polyhydroxylated pyrrolidines as a stabilizer of acid alpha-glucosidase (GAA) to enhance the efficacy of enzyme replacement therapy in Pompe disease
|
Li, Huang-Yi
|
|
|
78 |
C |
p.
|
artikel
|
| 18 |
Improved synthesis of deoxyalpinoid B and quantification of antileishmanial activity of deoxyalpinoid B and sulforaphane
|
Leary, Emma
|
|
|
78 |
C |
p.
|
artikel
|
| 19 |
Multitargeting approaches to cognitive impairment: Synthesis of aryl-alkylpiperazines and assessment at cholinesterases, histamine H3 and dopamine D3 receptors
|
Aranha, Cecília M.S.Q.
|
|
|
78 |
C |
p.
|
artikel
|
| 20 |
2′-N-Alkylaminocarbonyl-2′-amino-LNA: Synthesis, duplex stability, nuclease resistance, and in vitro anti-microRNA activity
|
Takegawa-Araki, Tomo
|
|
|
78 |
C |
p.
|
artikel
|
| 21 |
Neuritogenic steroid glycosides from crown-of-thorns starfish: Possible involvement of p38 mitogen-activated protein kinase and attenuation of cognitive impairment in senescence-accelerated mice (SAMP8) by peripheral administration
|
Sasayama, Yumi
|
|
|
78 |
C |
p.
|
artikel
|
| 22 |
Synthesis and biological evaluation of tert-butyl ester and ethyl ester prodrugs of L-γ-methyleneglutamic acid amides for cancer
|
Khan, Md Imdadul H.
|
|
|
78 |
C |
p.
|
artikel
|
| 23 |
Synthesis and biophysical properties of tetravalent PEG-conjugated antisense oligonucleotide
|
Rahman Chowdhury, Taslima
|
|
|
78 |
C |
p.
|
artikel
|
| 24 |
The effect of diphenylethane side-chain substituents on dibenzocyclohexadiene formation and their inhibition of α-synuclein aggregation in vitro
|
Bernardes, Gabriel
|
|
|
78 |
C |
p.
|
artikel
|
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