| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Biological activity of N(4)-boronated derivatives of 2′-deoxycytidine, potential agents for boron-neutron capture therapy
|
Nizioł, Joanna
|
|
2015
|
23 |
19 |
p. 6297-6304
8 p.
|
artikel
|
| 2 |
Curcumin-inspired cytotoxic 3,5-bis(arylmethylene)-1-(N-(ortho-substituted aryl)maleamoyl)-4-piperidones: A novel group of topoisomerase II alpha inhibitors
|
Jha, Amitabh
|
|
2015
|
23 |
19 |
p. 6404-6417
14 p.
|
artikel
|
| 3 |
Deprotometalation–iodolysis and computed CH acidity of 1,2,3- and 1,2,4-triazoles. Application to the synthesis of resveratrol analogues
|
Nagaradja, Elisabeth
|
|
2015
|
23 |
19 |
p. 6355-6363
9 p.
|
artikel
|
| 4 |
Design and synthesis of 4-benzylpiperidine carboxamides as dual serotonin and norepinephrine reuptake inhibitors
|
Paudel, Suresh
|
|
2015
|
23 |
19 |
p. 6418-6426
9 p.
|
artikel
|
| 5 |
Design and synthesis of conformationally constrained hydroxylated 4-phenyl-2-aryl chromenopyridines as novel and selective topoisomerase II-targeted antiproliferative agents
|
Thapa, Pritam
|
|
2015
|
23 |
19 |
p. 6454-6466
13 p.
|
artikel
|
| 6 |
Design, synthesis, and pharmacological evaluation of JDTic analogs to examine the significance of the 3- and 4-methyl substituents
|
Carroll, F. Ivy
|
|
2015
|
23 |
19 |
p. 6379-6388
10 p.
|
artikel
|
| 7 |
Development of N-hydroxybenzamide derivatives with indole-containing cap group as histone deacetylases inhibitors
|
Li, Xiaoyang
|
|
2015
|
23 |
19 |
p. 6258-6270
13 p.
|
artikel
|
| 8 |
Discovery and SAR of novel pyrazolo[1,5-a]pyrimidines as inhibitors of CDK9
|
Phillipson, Louisa J.
|
|
2015
|
23 |
19 |
p. 6280-6296
17 p.
|
artikel
|
| 9 |
Discovery and SAR study of 3-(tert-butyl)-4-hydroxyphenyl benzoate and benzamide derivatives as novel farnesoid X receptor (FXR) antagonists
|
Song, Kebiao
|
|
2015
|
23 |
19 |
p. 6427-6436
10 p.
|
artikel
|
| 10 |
Discovery of 4-benzoylamino-N-(prop-2-yn-1-yl)benzamides as novel microRNA-21 inhibitors
|
Jiang, Cong-shan
|
|
2015
|
23 |
19 |
p. 6510-6519
10 p.
|
artikel
|
| 11 |
Discovery of potent nitrotriazole-based antitrypanosomal agents: In vitro and in vivo evaluation
|
Papadopoulou , Maria V.
|
|
2015
|
23 |
19 |
p. 6467-6476
10 p.
|
artikel
|
| 12 |
Editorial board
|
|
|
2015
|
23 |
19 |
p. IFC-
1 p.
|
artikel
|
| 13 |
Graphical contents list
|
|
|
2015
|
23 |
19 |
p. 6229-6236
8 p.
|
artikel
|
| 14 |
Instructions to contributors
|
|
|
2015
|
23 |
19 |
p. I-
1 p.
|
artikel
|
| 15 |
Isolation and anticancer, anthelminthic, and antiviral (HIV) activity of acylphloroglucinols, and regioselective synthesis of empetrifranzinans from Hypericum roeperianum
|
Fobofou, Serge Alain Tanemossu
|
|
2015
|
23 |
19 |
p. 6327-6334
8 p.
|
artikel
|
| 16 |
Kinase hinge binding scaffolds and their hydrogen bond patterns
|
Xing, Li
|
|
2015
|
23 |
19 |
p. 6520-6527
8 p.
|
artikel
|
| 17 |
Multifunctional novel Diallyl disulfide (DADS) derivatives with β-amyloid-reducing, cholinergic, antioxidant and metal chelating properties for the treatment of Alzheimer’s disease
|
Manral, Apra
|
|
2015
|
23 |
19 |
p. 6389-6403
15 p.
|
artikel
|
| 18 |
New carbocyclic N6-substituted adenine and pyrimidine nucleoside analogues with a bicyclo[2.2.1]heptane fragment as sugar moiety; synthesis, antiviral, anticancer activity and X-ray crystallography
|
Tănase, Constantin I.
|
|
2015
|
23 |
19 |
p. 6346-6354
9 p.
|
artikel
|
| 19 |
Next generation macrocyclic and acyclic cationic lipids for gene transfer: Synthesis and in vitro evaluation
|
Jubeli, Emile
|
|
2015
|
23 |
19 |
p. 6364-6378
15 p.
|
artikel
|
| 20 |
Novel inhibitors targeting PPM1D phosphatase potently suppress cancer cell proliferation
|
Ogasawara, Sari
|
|
2015
|
23 |
19 |
p. 6246-6249
4 p.
|
artikel
|
| 21 |
Reengineered tricyclic anti-cancer agents
|
Kastrinsky, David B.
|
|
2015
|
23 |
19 |
p. 6528-6534
7 p.
|
artikel
|
| 22 |
Revisiting 1,3,4-Oxadiazol-2-ones: Utilization in the Development of ABHD6 Inhibitors
|
Patel, Jayendra Z.
|
|
2015
|
23 |
19 |
p. 6335-6345
11 p.
|
artikel
|
| 23 |
Synthesis and anticancer effects evaluation of 1-alkyl-3-(6-(2-methoxy-3-sulfonylaminopyridin-5-yl)benzo[d]thiazol-2-yl)urea as anticancer agents with low toxicity
|
Xie, Xiao-Xiao
|
|
2015
|
23 |
19 |
p. 6477-6485
9 p.
|
artikel
|
| 24 |
Synthesis and biological evaluation of novel 7-substituted 3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-4-amines as potent Bruton’s tyrosine kinase (BTK) inhibitors
|
Xin , Minhang
|
|
2015
|
23 |
19 |
p. 6250-6257
8 p.
|
artikel
|
| 25 |
Synthesis and structure–activity relationships of novel 9-oxime acylides with improved bactericidal activity
|
Han, Xu
|
|
2015
|
23 |
19 |
p. 6437-6453
17 p.
|
artikel
|
| 26 |
Synthesis, antiangiogenesis evaluation and molecular docking studies of 1-aryl-3-[(thieno[3,2-b]pyridin-7-ylthio)phenyl]ureas: Discovery of a new substitution pattern for type II VEGFR-2 Tyr kinase inhibitors
|
Machado, Vera A.
|
|
2015
|
23 |
19 |
p. 6497-6509
13 p.
|
artikel
|
| 27 |
Synthesis, antiproliferative activity and possible mechanism of action of novel 2-acetamidobenzamides bearing the 2-phenoxy functionality
|
Raffa , Demetrio
|
|
2015
|
23 |
19 |
p. 6305-6316
12 p.
|
artikel
|
| 28 |
Synthesis, electronic properties, antioxidant and antibacterial activity of some new benzimidazoles
|
Mavrova , Anelia Ts.
|
|
2015
|
23 |
19 |
p. 6317-6326
10 p.
|
artikel
|
| 29 |
Synthesis of a series of unsaturated ketone derivatives as selective and reversible monoamine oxidase inhibitors
|
Choi, Ji Won
|
|
2015
|
23 |
19 |
p. 6486-6496
11 p.
|
artikel
|
| 30 |
Synthesis of five and six-membered heterocycles bearing an arylpiperazinylalkyl side chain as orally active antinociceptive agents
|
Vergelli, Claudia
|
|
2015
|
23 |
19 |
p. 6237-6245
9 p.
|
artikel
|
| 31 |
Synthesis of new opioid derivatives with a propellane skeleton and their pharmacologies: Part 5, novel pentacyclic propellane derivatives with a 6-amide side chain
|
Nakajima, Ryo
|
|
2015
|
23 |
19 |
p. 6271-6279
9 p.
|
artikel
|
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