| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Comparative assessment of a 99mTc labeled H1299.2-HYNIC peptide bearing two different co-ligands for tumor-targeted imaging
|
Torabizadeh, Seyedeh Atekeh
|
|
2017
|
25 |
9 |
p. 2583-2592
10 p.
|
artikel
|
| 2 |
Corrigendum to “Synthesis and biological activity of 2,5-diaryl-3-methylpyrimido[4,5-c]quinolin-1(2H)-one derivatives” [Bioorg. Med. Chem. 15 (2007) 2434–2440]
|
Metwally, Kamel
|
|
2017
|
25 |
9 |
p. 2679-
1 p.
|
artikel
|
| 3 |
Development and crystallographic evaluation of histone H3 peptide with N-terminal serine substitution as a potent inhibitor of lysine-specific demethylase 1
|
Amano, Yuichi
|
|
2017
|
25 |
9 |
p. 2617-2624
8 p.
|
artikel
|
| 4 |
Development of N-hydroxycinnamamide-based HDAC inhibitors with improved HDAC inhibitory activity and in vitro antitumor activity
|
Zang, Jie
|
|
2017
|
25 |
9 |
p. 2666-2675
10 p.
|
artikel
|
| 5 |
Discovery of (2-aminophenyl)methanol as a new molecular chaperone that rescues the localization of P123S mutant pendrin stably expressed in HEK293 cells
|
Nabeyama, Wataru
|
|
2017
|
25 |
9 |
p. 2601-2608
8 p.
|
artikel
|
| 6 |
Discovery of a potent inhibitor of MELK that inhibits expression of the anti-apoptotic protein Mcl-1 and TNBC cell growth
|
Edupuganti, Ramakrishna
|
|
2017
|
25 |
9 |
p. 2609-2616
8 p.
|
artikel
|
| 7 |
Discovery of a series of 1,3,4-oxadiazole-2(3H)-thione derivatives containing piperazine skeleton as potential FAK inhibitors
|
Sun, Juan
|
|
2017
|
25 |
9 |
p. 2593-2600
8 p.
|
artikel
|
| 8 |
Editorial board
|
|
|
2017
|
25 |
9 |
p. IFC-
1 p.
|
artikel
|
| 9 |
Erratum to “Synthesis, biological evaluation, and physicochemical property assessment of 4-substituted 2-phenylaminoquinazolines as Mer tyrosine kinase inhibitors” [Bioorg. Med. Chem. 24 (2016) 3083–3092]
|
Wang, Sheng-Biao
|
|
2017
|
25 |
9 |
p. 2676-2678
3 p.
|
artikel
|
| 10 |
Indenocinnoline derivatives as G-quadruplex binders, topoisomerase IIα inhibitors and antiproliferative agents
|
Zoidis, Grigoris
|
|
2017
|
25 |
9 |
p. 2625-2634
10 p.
|
artikel
|
| 11 |
Indole-TEMPO conjugates alleviate ischemia-reperfusion injury via attenuation of oxidative stress and preservation of mitochondrial function
|
Bi, Wei
|
|
2017
|
25 |
9 |
p. 2545-2568
24 p.
|
artikel
|
| 12 |
Inhibition of Malassezia globosa carbonic anhydrase with phenols
|
Entezari Heravi, Yeganeh
|
|
2017
|
25 |
9 |
p. 2577-2582
6 p.
|
artikel
|
| 13 |
Inhibitors of nuclease and redox activity of apurinic/apyrimidinic endonuclease 1/redox effector factor 1 (APE1/Ref-1)
|
Laev, Sergey S.
|
|
2017
|
25 |
9 |
p. 2531-2544
14 p.
|
artikel
|
| 14 |
Inhibitors of protein arginine deiminases and their efficacy in animal models of multiple sclerosis
|
Sarswat, Amit
|
|
2017
|
25 |
9 |
p. 2643-2656
14 p.
|
artikel
|
| 15 |
Novel pyrazolo[1,5-a]pyridines as orally active EP1 receptor antagonists: Synthesis, structure-activity relationship studies, and biological evaluation
|
Umei, Kentaro
|
|
2017
|
25 |
9 |
p. 2635-2642
8 p.
|
artikel
|
| 16 |
Synthesis and carbonic anhydrase inhibition of a series of SLC-0111 analogs
|
Carta, Fabrizio
|
|
2017
|
25 |
9 |
p. 2569-2576
8 p.
|
artikel
|
| 17 |
Thiazolidine derivatives as potent and selective inhibitors of the PIM kinase family
|
Bataille, Carole J.R.
|
|
2017
|
25 |
9 |
p. 2657-2665
9 p.
|
artikel
|
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