| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Aib-containing peptide analogs: Cellular uptake and utilization in oligonucleotide delivery
|
Wada, Shun-ichi
|
|
2014
|
22 |
24 |
p. 6776-6780
5 p.
|
artikel
|
| 2 |
Almiramide D, cytotoxic peptide from the marine cyanobacterium Oscillatoria nigroviridis
|
Quintana, Jairo
|
|
2014
|
22 |
24 |
p. 6789-6795
7 p.
|
artikel
|
| 3 |
A new class of salicylic acid derivatives for inhibiting YopH of Yersinia pestis
|
Paudyal, Mahesh P.
|
|
2014
|
22 |
24 |
p. 6781-6788
8 p.
|
artikel
|
| 4 |
Anti-fibrillogenic properties of phthalocyanines: Effect of the out-of-plane ligands
|
Kovalska, V.
|
|
2014
|
22 |
24 |
p. 6918-6923
6 p.
|
artikel
|
| 5 |
Antitubercular activity of quinolizidinyl/pyrrolizidinylalkyliminophenazines
|
Tonelli, Michele
|
|
2014
|
22 |
24 |
p. 6837-6845
9 p.
|
artikel
|
| 6 |
Design and synthesis of 21-alkynylaryl pregnenolone derivatives and evaluation of their anticancer activity
|
Szalóki, György
|
|
2014
|
22 |
24 |
p. 6980-6988
9 p.
|
artikel
|
| 7 |
Design of a hydrogen peroxide-activatable agent that specifically targets cancer cells
|
Vadukoot, Anish K.
|
|
2014
|
22 |
24 |
p. 6885-6892
8 p.
|
artikel
|
| 8 |
Design, synthesis and evaluation of novel triazole core based P-glycoprotein-mediated multidrug resistance reversal agents
|
Jiao, Lei
|
|
2014
|
22 |
24 |
p. 6857-6866
10 p.
|
artikel
|
| 9 |
Design, synthesis, anticancer activity and docking studies of novel 4-morpholino-7,8-dihydro-5H-thiopyrano[4,3-d]pyrimidine derivatives as mTOR inhibitors
|
Zhu, Wufu
|
|
2014
|
22 |
24 |
p. 6746-6754
9 p.
|
artikel
|
| 10 |
Discovery of novel Bcr–Abl inhibitors targeting myristoyl pocket and ATP site
|
Dong, Jinyun
|
|
2014
|
22 |
24 |
p. 6876-6884
9 p.
|
artikel
|
| 11 |
Discovery of novel tetrahydroisoquinoline derivatives as orally active N-type calcium channel blockers with high selectivity for hERG potassium channels
|
Ogiyama, Takashi
|
|
2014
|
22 |
24 |
p. 6899-6907
9 p.
|
artikel
|
| 12 |
Editorial board
|
|
|
2014
|
22 |
24 |
p. IFC-
1 p.
|
artikel
|
| 13 |
4-Functionalized 1,3-diarylpyrazoles bearing 6-aminosulfonylbenzothiazole moiety as potent inhibitors of carbonic anhydrase isoforms hCA I, II, IX and XII
|
SitaRam,
|
|
2014
|
22 |
24 |
p. 6945-6952
8 p.
|
artikel
|
| 14 |
Glaser oxidative coupling on peptides: Stabilization of β-turn structure via a 1,3-butadiyne constraint
|
Auberger, Nicolas
|
|
2014
|
22 |
24 |
p. 6924-6932
9 p.
|
artikel
|
| 15 |
Graphical contents list
|
|
|
2014
|
22 |
24 |
p. 6727-6734
8 p.
|
artikel
|
| 16 |
Identification of novel 4-anilinoquinazoline derivatives as potent EGFR inhibitors both under normoxia and hypoxia
|
Cheng, Weiyan
|
|
2014
|
22 |
24 |
p. 6796-6805
10 p.
|
artikel
|
| 17 |
Inhibition studies of new ureido-substituted sulfonamides incorporating a GABA moiety against human carbonic anhydrase isoforms I–XIV
|
Ceruso, Mariangela
|
|
2014
|
22 |
24 |
p. 6768-6775
8 p.
|
artikel
|
| 18 |
New potent antibacterials against Gram-positive multiresistant pathogens: Effects of side chain modification and chirality in linezolid-like 1,2,4-oxadiazoles
|
Fortuna, Cosimo G.
|
|
2014
|
22 |
24 |
p. 6814-6825
12 p.
|
artikel
|
| 19 |
Novel derivatives of usnic acid effectively inhibiting reproduction of influenza A virus
|
Shtro, Anna A.
|
|
2014
|
22 |
24 |
p. 6826-6836
11 p.
|
artikel
|
| 20 |
Structural analogues of the natural products magnolol and honokiol as potent allosteric potentiators of GABAA receptors
|
Fuchs, Alexander
|
|
2014
|
22 |
24 |
p. 6908-6917
10 p.
|
artikel
|
| 21 |
Synthesis and antitumor activity of novel 1-substituted phenyl 3-(2-oxo-1,3,4-oxadiazol-5-yl) β-carbolines and their Mannich bases
|
Savariz, Franciele Cristina
|
|
2014
|
22 |
24 |
p. 6867-6875
9 p.
|
artikel
|
| 22 |
Synthesis and antiviral activities of 3-deaza-3-fluoroaristeromycin and its 5′ analogues
|
Chen, Qi
|
|
2014
|
22 |
24 |
p. 6961-6964
4 p.
|
artikel
|
| 23 |
Synthesis and biological evaluation of novel oxindole-based RTK inhibitors as anti-cancer agents
|
Chen, Gaozhi
|
|
2014
|
22 |
24 |
p. 6953-6960
8 p.
|
artikel
|
| 24 |
Synthesis and evaluation of N-acyl-substituted 1,2-benzisothiazol-3-one derivatives as caspase-3 inhibitors
|
Li, Zhenghui
|
|
2014
|
22 |
24 |
p. 6735-6745
11 p.
|
artikel
|
| 25 |
Synthesis and evaluation of the 2,4-diaminoquinazoline series as anti-tubercular agents
|
Odingo, Joshua
|
|
2014
|
22 |
24 |
p. 6965-6979
15 p.
|
artikel
|
| 26 |
Synthesis, anti-inflammatory activity and modeling studies of cycloartane-type terpenes derivatives isolated from Parthenium argentatum
|
Romero, Juan Carlos
|
|
2014
|
22 |
24 |
p. 6893-6898
6 p.
|
artikel
|
| 27 |
Synthesis, in vitro and in vivo studies, and molecular modeling of N-alkylated dextromethorphan derivatives as non-competitive inhibitors of α3β4 nicotinic acetylcholine receptor
|
Jozwiak, Krzysztof
|
|
2014
|
22 |
24 |
p. 6846-6856
11 p.
|
artikel
|
| 28 |
Synthesis of aminoacylated N 6,N 6-dimethyladenosine solid support for efficient access to hydrolysis-resistant 3′-charged tRNA mimics
|
Neuner, Sandro
|
|
2014
|
22 |
24 |
p. 6989-6995
7 p.
|
artikel
|
| 29 |
Synthesis of 2-anilinopyridine dimers as microtubule targeting and apoptosis inducing agents
|
Kamal, Ahmed
|
|
2014
|
22 |
24 |
p. 6755-6767
13 p.
|
artikel
|
| 30 |
Synthesis of multi-galactose-conjugated 2′-O-methyl oligoribonucleotides and their in vivo imaging with positron emission tomography
|
Mäkilä, Jussi
|
|
2014
|
22 |
24 |
p. 6806-6813
8 p.
|
artikel
|
| 31 |
Targeting (cellular) lysosomal acid ceramidase by B13: Design, synthesis and evaluation of novel DMG-B13 ester prodrugs
|
Bai, Aiping
|
|
2014
|
22 |
24 |
p. 6933-6944
12 p.
|
artikel
|
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