| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acridin-3,6-dialkyldithiourea hydrochlorides as new photosensitizers for photodynamic therapy of mouse leukemia cells
|
Cisáriková, A.
|
|
2016
|
24 |
9 |
p. 2011-2022
12 p.
|
artikel
|
| 2 |
Design, synthesis and anti-HIV-1 evaluation of hydrazide-based peptidomimetics as selective gelatinase inhibitors
|
Yang, Liang
|
|
2016
|
24 |
9 |
p. 2125-2136
12 p.
|
artikel
|
| 3 |
Design, synthesis and biological evaluation of 5-amino-4-(1H-benzoimidazol-2-yl)-phenyl-1,2-dihydro-pyrrol-3-ones as inhibitors of protein kinase FGFR1
|
Gryshchenko, A.A.
|
|
2016
|
24 |
9 |
p. 2053-2059
7 p.
|
artikel
|
| 4 |
Design, synthesis, and biological evaluation of arylpiperazine–benzylpiperidines with dual serotonin and norepinephrine reuptake inhibitory activities
|
Paudel, Suresh
|
|
2016
|
24 |
9 |
p. 2137-2145
9 p.
|
artikel
|
| 5 |
Design, synthesis, and evaluation of hinge-binder tethered 1,2,3-triazolylsalicylamide derivatives as Aurora kinase inhibitors
|
Jeong, Yunkyung
|
|
2016
|
24 |
9 |
p. 2114-2124
11 p.
|
artikel
|
| 6 |
Design, synthesis, assessment, and molecular docking of novel pyrrolopyrimidine (7-deazapurine) derivatives as non-nucleoside hepatitis C virus NS5B polymerase inhibitors
|
Mohamed, Mosaad S.
|
|
2016
|
24 |
9 |
p. 2146-2157
12 p.
|
artikel
|
| 7 |
Development of a 3′-amino linker with high conjugation activity and its application to conveniently cross-link blunt ends of a duplex
|
Kowata, Keiko
|
|
2016
|
24 |
9 |
p. 2108-2113
6 p.
|
artikel
|
| 8 |
Discovery of novel pyrrole-based scaffold as potent and orally bioavailable free fatty acid receptor 1 agonists for the treatment of type 2 diabetes
|
Li, Zheng
|
|
2016
|
24 |
9 |
p. 1981-1987
7 p.
|
artikel
|
| 9 |
Editorial board
|
|
|
2016
|
24 |
9 |
p. IFC-
1 p.
|
artikel
|
| 10 |
Exploration of the P3 region of PEXEL peptidomimetics leads to a potent inhibitor of the Plasmodium protease, plasmepsin V
|
Gazdik, Michelle
|
|
2016
|
24 |
9 |
p. 1993-2010
18 p.
|
artikel
|
| 11 |
Investigation of human flap structure-specific endonuclease 1 (FEN1) activity on primer-template models and exploration of a substrate-based FEN1 inhibitor
|
Ba, Sai
|
|
2016
|
24 |
9 |
p. 1988-1992
5 p.
|
artikel
|
| 12 |
Synthesis and antitumor activity evaluation of a novel combi-nitrosourea prodrug: Designed to release a DNA cross-linking agent and an inhibitor of O6-alkylguanine-DNA alkyltransferase
|
Sun, Guohui
|
|
2016
|
24 |
9 |
p. 2097-2107
11 p.
|
artikel
|
| 13 |
Synthesis and evaluation of 6-(3-[18F]fluoro-2-hydroxypropyl)-substituted 2-pyridylbenzothiophenes and 2-pyridylbenzothiazoles as potential PET tracers for imaging Aβ plaques
|
Lee, Byoung Se
|
|
2016
|
24 |
9 |
p. 2043-2052
10 p.
|
artikel
|
| 14 |
Synthesis and evaluation of novel angiotensin II receptor 1 antagonists as anti-hypertension drugs
|
Bao, Xiaolu
|
|
2016
|
24 |
9 |
p. 2023-2031
9 p.
|
artikel
|
| 15 |
Synthesis, anti-inflammatory, analgesic, COX-1/2 inhibition activities and molecular docking study of pyrazoline derivatives
|
Abdel-Sayed, Maged A.
|
|
2016
|
24 |
9 |
p. 2032-2042
11 p.
|
artikel
|
| 16 |
Synthesis of 4-substituted nipecotic acid derivatives and their evaluation as potential GABA uptake inhibitors
|
Hellenbrand, Tim
|
|
2016
|
24 |
9 |
p. 2072-2096
25 p.
|
artikel
|
| 17 |
Synthetic approaches to the 2014 new drugs
|
Flick, Andrew C.
|
|
2016
|
24 |
9 |
p. 1937-1980
44 p.
|
artikel
|
| 18 |
Tetrahydroprotoberberine alkaloids with dopamine and σ receptor affinity
|
Gadhiya, Satishkumar
|
|
2016
|
24 |
9 |
p. 2060-2071
12 p.
|
artikel
|
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