| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Attaching palladium catalysts to antibodies
|
Cowling, Paul
|
|
|
44 |
C |
p.
|
artikel
|
| 2 |
A versatile toolbox for investigating biological processes based on quinone methide chemistry: From self-immolative linkers to self-immobilizing agents
|
Abe, Atsuki
|
|
|
44 |
C |
p.
|
artikel
|
| 3 |
Click, release, and fluoresce: In-vivo generation of CO with concomitant synthesis of a fluorescent reporter
|
De La Cruz, Ladie Kimberly
|
|
|
44 |
C |
p.
|
artikel
|
| 4 |
De novo design with deep generative models based on 3D similarity scoring
|
Papadopoulos, Kostas
|
|
|
44 |
C |
p.
|
artikel
|
| 5 |
Design, synthesis and biochemical evaluation of novel carbonic anhydrase inhibitors triggered by structural knowledge on hCA VII
|
Mancuso, Francesca
|
|
|
44 |
C |
p.
|
artikel
|
| 6 |
Design, synthesis and biological evaluation of double fatty chain-modified glucagon-like peptide-1 conjugates
|
Zhang, Jinhua
|
|
|
44 |
C |
p.
|
artikel
|
| 7 |
Design, synthesis and biological evaluation of 2-styryl-5-hydroxy-4-pyrone derivatives and analogues as multiple functional agents with the potential for the treatment of Alzheimer’s disease
|
Hu, Chenxian
|
|
|
44 |
C |
p.
|
artikel
|
| 8 |
Dithiolated peptides incorporating bis(tryptophan)s for cooperative mercury(II) binding
|
Ngu-Schwemlein, Maria
|
|
|
44 |
C |
p.
|
artikel
|
| 9 |
Dual Bcl-XL /Bcl-2 inhibitors discovered from DNA-encoded libraries using a fragment pairing strategy
|
Daguer, Jean-Pierre
|
|
|
44 |
C |
p.
|
artikel
|
| 10 |
Editorial Board
|
|
|
|
44 |
C |
p.
|
artikel
|
| 11 |
Evaluation of artemisinin derivative artemether as a fluconazole potentiator through inhibition of Pdr5
|
Zhou, Jia
|
|
|
44 |
C |
p.
|
artikel
|
| 12 |
Fragment-based lead discovery to identify novel inhibitors that target the ATP binding site of pyruvate dehydrogenase kinases
|
Akaki, Tatsuo
|
|
|
44 |
C |
p.
|
artikel
|
| 13 |
Graphical Abstract Contents Continued
|
|
|
|
44 |
C |
p.
|
artikel
|
| 14 |
Graphical abstract TOC
|
|
|
|
44 |
C |
p.
|
artikel
|
| 15 |
Graphical abstract TOC
|
|
|
|
44 |
C |
p.
|
artikel
|
| 16 |
Impact of α-modifications on the activity of triazole bisphosphonates as geranylgeranyl diphosphate synthase inhibitors
|
Fairweather, Alisa E.R.
|
|
|
44 |
C |
p.
|
artikel
|
| 17 |
Inhibitory activities of anthraquinone and xanthone derivatives against transthyretin amyloidogenesis
|
Kitakami, Ryota
|
|
|
44 |
C |
p.
|
artikel
|
| 18 |
Larvicidal activity and in silico studies of cinnamic acid derivatives against Aedes aegypti (Diptera: Culicidae)
|
Bezerra França, Saraliny
|
|
|
44 |
C |
p.
|
artikel
|
| 19 |
Optimization of 1,4-bis(arylsulfonamido)naphthalene-N,N'-diacetic acids as inhibitors of Keap1-Nrf2 protein-protein interaction to suppress neuroinflammation
|
Abed, Dhulfiqar Ali
|
|
|
44 |
C |
p.
|
artikel
|
| 20 |
Pyrrolo[1,2-a]quinoxal-5-inium salts and 4,5-dihydropyrrolo[1,2-a]quinoxalines: Synthesis, activity and computational docking for protein tyrosine phosphatase 1B
|
Sánchez-Alonso, Patricia
|
|
|
44 |
C |
p.
|
artikel
|
| 21 |
Quantum mechanical study on the activation mechanism of human carbonic anhydrase VII cluster model with bis-histamine schiff bases and bis-spinaceamine derivatives
|
Ghiasi, Mina
|
|
|
44 |
C |
p.
|
artikel
|
| 22 |
Self-assembly of photosensitive and radiotherapeutic peptide for combined photodynamic-radio cancer therapy with intracellular delivery of miRNA-139-5p
|
Wang, Hanhua
|
|
|
44 |
C |
p.
|
artikel
|
| 23 |
Structural insights in galectin-1-glycan recognition: Relevance of the glycosidic linkage and the N-acetylation pattern of sugar moieties
|
Porciúncula-González, Cecilia
|
|
|
44 |
C |
p.
|
artikel
|
| 24 |
Synthesis and characterization of a new two photon excitable acid sphingomyelinase FRET probe
|
Mohamed, Zain H.
|
|
|
44 |
C |
p.
|
artikel
|
| 25 |
Synthesis and interaction of terminal unsaturated chemical probes with Mycobacterium tuberculosis CYP124A1
|
Díaz-Storani, Luz
|
|
|
44 |
C |
p.
|
artikel
|
| 26 |
Synthesis, bioevaluation and docking studies of new imidamide derivatives as nitric oxide synthase inhibitors
|
Arias, Fabio
|
|
|
44 |
C |
p.
|
artikel
|
| 27 |
Utilizing structure based drug design and metabolic soft spot identification to optimize the in vitro potency and in vivo pharmacokinetic properties leading to the discovery of novel reversible Bruton’s tyrosine kinase inhibitors
|
Hopkins, Brian T.
|
|
|
44 |
C |
p.
|
artikel
|
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