| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An appraisal on synthetic and pharmaceutical perspectives of pyrazolo[4,3-d]pyrimidine scaffold
|
Cherukupalli, Srinivasulu
|
|
|
26 |
2 |
p. 309-339
|
artikel
|
| 2 |
Bombesin/oligoarginine fusion peptides for gastrin releasing peptide receptor (GRPR) targeted gene delivery
|
Begum, Anjuman Ara
|
|
|
26 |
2 |
p. 516-526
|
artikel
|
| 3 |
Cellular imaging using BODIPY-, pyrene- and phthalocyanine-based conjugates
|
Bizet, Faustine
|
|
|
26 |
2 |
p. 413-420
|
artikel
|
| 4 |
Characterization of tyrosinase inhibitory constituents from the aerial parts of Humulus japonicus using LC-MS/MS coupled online assay
|
Yang, Hyo Hee
|
|
|
26 |
2 |
p. 509-515
|
artikel
|
| 5 |
Current knowledge on the nucleotide agonists for the P2Y2 receptor
|
Xu, Pengfei
|
|
|
26 |
2 |
p. 366-375
|
artikel
|
| 6 |
Design, synthesis and pharmacological evaluation of new acyl sulfonamides as potent and selective Bcl-2 inhibitors
|
Liu, Xiaohua
|
|
|
26 |
2 |
p. 443-454
|
artikel
|
| 7 |
Discovery of novel scaffolds for γ-secretase modulators without an arylimidazole moiety
|
Sekioka, Ryuichi
|
|
|
26 |
2 |
p. 435-442
|
artikel
|
| 8 |
Discovery of orally efficacious RORγt inverse agonists. Part 2: Design, synthesis, and biological evaluation of novel tetrahydroisoquinoline derivatives
|
Kono, Mitsunori
|
|
|
26 |
2 |
p. 470-482
|
artikel
|
| 9 |
Discovery of orally efficacious RORγt inverse agonists, part 1: Identification of novel phenylglycinamides as lead scaffolds
|
Shirai, Junya
|
|
|
26 |
2 |
p. 483-500
|
artikel
|
| 10 |
1,5-Disubstituted 1,2,3-triazole linked disaccharides: Metal-free syntheses and screening of a new class of ribonuclease A inhibitors
|
Kayet, Anirban
|
|
|
26 |
2 |
p. 455-462
|
artikel
|
| 11 |
Editorial Board
|
|
|
|
26 |
2 |
p. ii
|
artikel
|
| 12 |
Evaluation of 18F-labeled exendin(9-39) derivatives targeting glucagon-like peptide-1 receptor for pancreatic β-cell imaging
|
Kimura, Hiroyuki
|
|
|
26 |
2 |
p. 463-469
|
artikel
|
| 13 |
Graphical abstract TOC
|
|
|
|
26 |
2 |
p. IBC
|
artikel
|
| 14 |
Graphical abstract TOC
|
|
|
|
26 |
2 |
p. OBC
|
artikel
|
| 15 |
Graphical abstract TOC continued
|
|
|
|
26 |
2 |
p. I-IV
|
artikel
|
| 16 |
5-HT1A and 5-HT2A receptors affinity, docking studies and pharmacological evaluation of a series of 8-acetyl-7-hydroxy-4-methylcoumarin derivatives
|
Ostrowska, Kinga
|
|
|
26 |
2 |
p. 527-535
|
artikel
|
| 17 |
Immunoproteasome inhibition and bioactivity of thiasyrbactins
|
Bakas, Nicole A.
|
|
|
26 |
2 |
p. 401-412
|
artikel
|
| 18 |
α-Methylation enhances the potency of isoprenoid triazole bisphosphonates as geranylgeranyl diphosphate synthase inhibitors
|
Matthiesen, Robert A.
|
|
|
26 |
2 |
p. 376-385
|
artikel
|
| 19 |
2-Methyltetrahydro-3-benzazepin-1-ols – The missing link in SAR of GluN2B selective NMDA receptor antagonists
|
Dey, Sougata
|
|
|
26 |
2 |
p. 501-508
|
artikel
|
| 20 |
Monoterpene indole alkaloid azine derivatives as MDR reversal agents
|
Paterna, Angela
|
|
|
26 |
2 |
p. 421-434
|
artikel
|
| 21 |
Natural products as sources of new fungicides (IV): Synthesis and biological evaluation of isobutyrophenone analogs as potential inhibitors of class-II fructose-1,6-bisphosphate aldolase
|
Li, Ding
|
|
|
26 |
2 |
p. 386-393
|
artikel
|
| 22 |
Podophyllotoxin derivatives as an excellent anticancer aspirant for future chemotherapy: A key current imminent needs
|
Zhang, Xu
|
|
|
26 |
2 |
p. 340-355
|
artikel
|
| 23 |
Selective inhibition of β-N-acetylhexosaminidases by thioglycosyl–naphthalimide hybrid molecules
|
Chen, Wei
|
|
|
26 |
2 |
p. 394-400
|
artikel
|
| 24 |
Synthesis, structure-activity relationships, and mechanistic studies of 5-arylazo-tropolone derivatives as novel xanthine oxidase (XO) inhibitors
|
Sato, Daisuke
|
|
|
26 |
2 |
p. 536-542
|
artikel
|
| 25 |
Targeting protein-protein interaction between MLL1 and reciprocal proteins for leukemia therapy
|
Wang, Zhi-Hui
|
|
|
26 |
2 |
p. 356-365
|
artikel
|
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