| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Antiplasmodial activity of hydroxyethylamine analogs: Synthesis, biological activity and structure activity relationship of plasmepsin inhibitors
|
Kumar Singh, Amit
|
|
2018
|
26 |
13 |
p. 3837-3844
|
artikel
|
| 2 |
Corrigendum to “2-Arylthio-5-iodo pyrimidine derivatives as non-nucleoside HBV polymerase inhibitors” [Bioorg. Med. Chem. 26 (2018) 1573–1578]
|
Wang, Jie
|
|
2018
|
26 |
13 |
p. 3859
|
artikel
|
| 3 |
Corrigendum to “Nrf2 activators from Glycyrrhiza inflata and their hepatoprotective activities against CCl4-induced liver injury in mice” [Bioorg. Med. Chem. 25 (20) (2017) 5522–5530]
|
Lin, Yan
|
|
2018
|
26 |
13 |
p. 3858
|
artikel
|
| 4 |
Corrigendum to “Synthesis, structure-activity relationship and molecular docking studies of 3-O-flavonol glycosides as cholinesterase inhibitors” [Bioorg. Med. Chem. 26 (12) (2018) 3696–3706]
|
Ullah Mughal, Ehsan
|
|
2018
|
26 |
13 |
p. 3860
|
artikel
|
| 5 |
Design, synthesis and cardiovascular evaluation of some aminoisopropanoloxy derivatives of xanthone
|
Kubacka, M.
|
|
2018
|
26 |
13 |
p. 3773-3784
|
artikel
|
| 6 |
Design, synthesis and evaluation of novel bivalent β-carboline derivatives as multifunctional agents for the treatment of Alzheimer's disease
|
Zhao, Yifan
|
|
2018
|
26 |
13 |
p. 3812-3824
|
artikel
|
| 7 |
Developing hybrid molecule therapeutics for diverse enzyme inhibitory action: Active role of coumarin-based structural leads in drug discovery
|
Ibrar, Aliya
|
|
2018
|
26 |
13 |
p. 3731-3762
|
artikel
|
| 8 |
Editorial Board
|
|
|
2018
|
26 |
13 |
p. ii
|
artikel
|
| 9 |
Graphical abstract TOC
|
|
|
2018
|
26 |
13 |
p. OBC
|
artikel
|
| 10 |
Graphical abstract TOC
|
|
|
2018
|
26 |
13 |
p. IBC
|
artikel
|
| 11 |
Graphical abstract TOC
|
|
|
2018
|
26 |
13 |
p. III-IV
|
artikel
|
| 12 |
New somatostatin-drug conjugates for effective targeting pancreatic cancer
|
Ragozin, E.
|
|
2018
|
26 |
13 |
p. 3825-3836
|
artikel
|
| 13 |
Novel androgen receptor full antagonists: Design, synthesis, and a docking study of glycerol and aminoglycerol derivatives that contain p-carborane cages
|
Kaise, Asako
|
|
2018
|
26 |
13 |
p. 3805-3811
|
artikel
|
| 14 |
Polysaccharide deacetylases serve as new targets for the design of inhibitors against Bacillus anthracis and Bacillus cereus
|
Balomenou, Stavroula
|
|
2018
|
26 |
13 |
p. 3845-3851
|
artikel
|
| 15 |
Sameuramide A, a new cyclic depsipeptide isolated from an ascidian of the family Didemnidae
|
Machida, Koshi
|
|
2018
|
26 |
13 |
p. 3852-3857
|
artikel
|
| 16 |
Synthesis, in vitro and in silico studies of novel potent urease inhibitors: N-[4-({5-[(3-Un/substituted-anilino-3-oxopropyl)sulfanyl]-1,3,4-oxadiazol-2-yl}methyl)-1,3-thiazol-2-yl]benzamides
|
Abbasi, Muhammad Athar
|
|
2018
|
26 |
13 |
p. 3791-3804
|
artikel
|
| 17 |
Synthesis of and triplex formation in oligonucleotides containing 2′-deoxy-6-thioxanthosine
|
Inde, Takeshi
|
|
2018
|
26 |
13 |
p. 3785-3790
|
artikel
|
| 18 |
Synthesis of 1,5-Anhydro-d-fructose derivatives and evaluation of their inflammasome inhibitors
|
Goto, Kohtaro
|
|
2018
|
26 |
13 |
p. 3763-3772
|
artikel
|
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