| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A brief overview on recent advances in spiro[chromane-2,4′-piperidine]-4(3H)-one-functionalized compounds in medicinal chemistry research
|
Ghatpande, Nitin G.
|
|
|
28 |
23 |
p.
|
artikel
|
| 2 |
Ahp-Cyclodepsipeptides as tunable inhibitors of human neutrophil elastase and kallikrein 7: Total synthesis of tutuilamide A, serine protease selectivity profile and comparison with lyngbyastatin 7
|
Chen, Qi-Yin
|
|
|
28 |
23 |
p.
|
artikel
|
| 3 |
A look around the West Indies: The spices of life are secondary metabolites
|
Demeritte, Adrian
|
|
|
28 |
23 |
p.
|
artikel
|
| 4 |
Andrographolide suppresses cisplatin-induced endothelial hyperpermeability through activation of PI3K/Akt and eNOS –derived nitric oxide
|
Bodiga, Vijaya Lakshmi
|
|
|
28 |
23 |
p.
|
artikel
|
| 5 |
Antibody drug conjugates of cleavable amino-benzoyl-maytansinoids
|
Nittoli, Thomas
|
|
|
28 |
23 |
p.
|
artikel
|
| 6 |
Chemical synthesis and biochemical characterization of cyclic oligonucleotides containing acyl groups at both 5′- and 3′-terminal positions
|
Nishizawa, Shuhei
|
|
|
28 |
23 |
p.
|
artikel
|
| 7 |
COVID-19 therapy: What weapons do we bring into battle?
|
de Almeida, Sinara Mônica Vitalino
|
|
|
28 |
23 |
p.
|
artikel
|
| 8 |
Design, synthesis and biological activity of bicyclic carboxamide derivatives as TRK inhibitors
|
Sun, Minghao
|
|
|
28 |
23 |
p.
|
artikel
|
| 9 |
Design, synthesis and biological evaluation of vortioxetine derivatives as new COX-1/2 inhibitors in human monocytes
|
Talmon, Maria
|
|
|
28 |
23 |
p.
|
artikel
|
| 10 |
Design, synthesis, and structure activity relationship (SAR) studies of novel imidazo[1,2-a] pyridine derivatives as Nek2 inhibitors
|
Wang, Haili
|
|
|
28 |
23 |
p.
|
artikel
|
| 11 |
Discovery of novel steroidal-chalcone hybrids with potent and selective activity against triple-negative breast cancer
|
Hou, Qiangqiang
|
|
|
28 |
23 |
p.
|
artikel
|
| 12 |
Discovery of thienothiazolocarboxamide analogues as novel anti-tubercular agent
|
Jin, Guanghai
|
|
|
28 |
23 |
p.
|
artikel
|
| 13 |
Disulfide bridge cross-linking between protein and the RNA backbone as a tool to study RNase H1
|
Hyjek-Składanowska, Malwina
|
|
|
28 |
23 |
p.
|
artikel
|
| 14 |
Divinylsulfonamides enable the construction of homogeneous antibody–drug conjugates
|
Huang, Rong
|
|
|
28 |
23 |
p.
|
artikel
|
| 15 |
Editorial Board
|
|
|
|
28 |
23 |
p.
|
artikel
|
| 16 |
Graphical abstract TOC
|
|
|
|
28 |
23 |
p.
|
artikel
|
| 17 |
Graphical abstract TOC
|
|
|
|
28 |
23 |
p.
|
artikel
|
| 18 |
Improving metabolic stability and removing aldehyde oxidase liability in a 5-azaquinazoline series of IRAK4 inhibitors
|
Degorce, Sébastien L.
|
|
|
28 |
23 |
p.
|
artikel
|
| 19 |
Nitrogen-containing naringenin derivatives for reversing multidrug resistance in cancer
|
Ferreira, Ricardo J.
|
|
|
28 |
23 |
p.
|
artikel
|
| 20 |
Novel thiobarbiturates as potent urease inhibitors with potential antibacterial activity: Design, synthesis, radiolabeling and biodistribution study
|
Abdulwahab, Hanan Gaber
|
|
|
28 |
23 |
p.
|
artikel
|
| 21 |
Optimization of kinetic stabilizers of tetrameric transthyretin: A prospective ligand efficiency-guided approach
|
Cotrina, Ellen Y.
|
|
|
28 |
23 |
p.
|
artikel
|
| 22 |
Preventing Candida albicans biofilm formation using aromatic-rich piperazines
|
Simon, Gaëlle
|
|
|
28 |
23 |
p.
|
artikel
|
| 23 |
Structural basis for stabilization of human telomeric G-quadruplex [d-(TTAGGGT)]4 by anticancer drug epirubicin
|
Barthwal, Ritu
|
|
|
28 |
23 |
p.
|
artikel
|
| 24 |
Studies on fragment-based design of allosteric inhibitors of human factor XIa
|
Boothello, Rio S.
|
|
|
28 |
23 |
p.
|
artikel
|
| 25 |
Study of triaryl-based sulfamic acid derivatives as HPTPβ inhibitors
|
Zhang, Wenjuan
|
|
|
28 |
23 |
p.
|
artikel
|
| 26 |
Synthesis and optimisation of P 3 substituted vinyl sulfone-based inhibitors as anti-trypanosomal agents
|
Doherty, William
|
|
|
28 |
23 |
p.
|
artikel
|
| 27 |
Synthesis, characterization, and fungicidal activity of novel Fangchinoline derivatives
|
Wang, Qi
|
|
|
28 |
23 |
p.
|
artikel
|
| 28 |
Synthesis of C-nucleoside analogues based on the pyrimidine skeleton for the formation of anti-parallel-type triplex DNA with a CG mismatch site
|
Notomi, Ryotaro
|
|
|
28 |
23 |
p.
|
artikel
|
| 29 |
The exploration of aza-quinolines as hematopoietic prostaglandin D synthase (H-PGDS) inhibitors with low brain exposure
|
Cadilla, Rodolfo
|
|
|
28 |
23 |
p.
|
artikel
|
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