nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Acetylcholinesterase and carbonic anhydrase inhibitory properties of novel urea and sulfamide derivatives incorporating dopaminergic 2-aminotetralin scaffolds
|
Özgeriş, Bünyamin |
|
2016 |
24 |
10 |
p. 2318-2329 12 p. |
artikel |
2 |
Biological evaluation of synthetic α,β-unsaturated carbonyl based cyclohexanone derivatives as neuroprotective novel inhibitors of acetylcholinesterase, butyrylcholinesterase and amyloid-β aggregation
|
Zha, Gao-Feng |
|
2016 |
24 |
10 |
p. 2352-2359 8 p. |
artikel |
3 |
Design, synthesis and biological evaluation of LBM-A5 derivatives as potent P-glycoprotein-mediated multidrug resistance inhibitors
|
Wu, Yuxiang |
|
2016 |
24 |
10 |
p. 2287-2297 11 p. |
artikel |
4 |
Development of 99mTc-labeled asymmetric urea derivatives that target prostate-specific membrane antigen for single-photon emission computed tomography imaging
|
Kimura, Hiroyuki |
|
2016 |
24 |
10 |
p. 2251-2256 6 p. |
artikel |
5 |
Editorial board
|
|
|
2016 |
24 |
10 |
p. IFC- 1 p. |
artikel |
6 |
Inhibitory effect of flavonoids on human glutaminyl cyclase
|
Li, Manman |
|
2016 |
24 |
10 |
p. 2280-2286 7 p. |
artikel |
7 |
N-Indolylglycosides bearing modifications at the glucose C6-position as sodium-dependent glucose co-transporter 2 inhibitors
|
Chu, Kuang-Feng |
|
2016 |
24 |
10 |
p. 2242-2250 9 p. |
artikel |
8 |
Orally bioavailable pyridine and pyrimidine-based Factor XIa inhibitors: Discovery of the methyl N-phenyl carbamate P2 prime group
|
Corte, James R. |
|
2016 |
24 |
10 |
p. 2257-2272 16 p. |
artikel |
9 |
Purinylpyridinylamino-based DFG-in/αC-helix-out B-Raf inhibitors: Applying mutant versus wild-type B-Raf selectivity indices for compound profiling
|
Liu, Longbin |
|
2016 |
24 |
10 |
p. 2215-2234 20 p. |
artikel |
10 |
Short cationic lipopeptides as effective antibacterial agents: Design, physicochemical properties and biological evaluation
|
Azmi, Fazren |
|
2016 |
24 |
10 |
p. 2235-2241 7 p. |
artikel |
11 |
Studies on phenothiazines: New microtubule-interacting compounds with phenothiazine A-ring as potent antineoplastic agents
|
Ghinet, Alina |
|
2016 |
24 |
10 |
p. 2307-2317 11 p. |
artikel |
12 |
Synthesis and anticancer activity of some 5-fluoro-2′-deoxyuridine phosphoramidates
|
Lewandowska, Marta |
|
2016 |
24 |
10 |
p. 2330-2341 12 p. |
artikel |
13 |
Synthesis and evaluation of 4-hydroxyl aurone derivatives as multifunctional agents for the treatment of Alzheimer’s disease
|
Li, Yan |
|
2016 |
24 |
10 |
p. 2342-2351 10 p. |
artikel |
14 |
Synthesis and evaluation of novel opioid ligands with a C-homomorphinan skeleton
|
Ishikawa, Kyoko |
|
2016 |
24 |
10 |
p. 2199-2205 7 p. |
artikel |
15 |
Synthesis and molecular docking of N′-arylidene-5-(4-chlorophenyl)-1-(3,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carbohydrazides as novel hypoglycemic and antioxidant dual agents
|
Hernández-Vázquez, Eduardo |
|
2016 |
24 |
10 |
p. 2298-2306 9 p. |
artikel |
16 |
Synthesis, identification, and biological activity of metabolites of two novel selective S1P1 agonists
|
Xiao, Qiong |
|
2016 |
24 |
10 |
p. 2273-2279 7 p. |
artikel |
17 |
The Cu/ligand stoichiometry effect on the coordination behavior of aroyl hydrazone with copper(II): Structure, anticancer activity and anticancer mechanism
|
Deng, JunGang |
|
2016 |
24 |
10 |
p. 2190-2198 9 p. |
artikel |
18 |
Towards understanding the unbound state of drug compounds: Implications for the intramolecular reorganization energy upon binding
|
Foloppe, Nicolas |
|
2016 |
24 |
10 |
p. 2159-2189 31 p. |
artikel |
19 |
Tumour-specific cytotoxicity and structure–activity relationships of novel 1-[3-(2-methoxyethylthio)propionyl]-3,5-bis(benzylidene)-4-piperidones
|
Hossain, Mohammad |
|
2016 |
24 |
10 |
p. 2206-2214 9 p. |
artikel |