| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
3,5-Bis(benzylidene)-4-piperidones and related N-acyl analogs: A novel cluster of antimalarials targeting the liver stage of Plasmodium falciparum
|
Das, Umashankar
|
|
2013
|
21 |
23 |
p. 7250-7256
7 p.
|
artikel
|
| 2 |
Bis-phosphonium salts of pyridoxine: The relationship between structure and antibacterial activity
|
Pugachev, Mikhail V.
|
|
2013
|
21 |
23 |
p. 7330-7342
13 p.
|
artikel
|
| 3 |
Design and evaluation of xanthine based adenosine receptor antagonists: Potential hypoxia targeted immunotherapies
|
Thomas, Rhiannon
|
|
2013
|
21 |
23 |
p. 7453-7464
12 p.
|
artikel
|
| 4 |
Design and synthesis of silicon-containing tubulin polymerization inhibitors: Replacement of the ethylene moiety of combretastatin A-4 with a silicon linker
|
Nakamura, Masaharu
|
|
2013
|
21 |
23 |
p. 7381-7391
11 p.
|
artikel
|
| 5 |
Design of fluorinated 5-HT4R antagonists: Influence of the basicity and lipophilicity toward the 5-HT4R binding affinities
|
Fontenelle, Clement Q.
|
|
2013
|
21 |
23 |
p. 7529-7538
10 p.
|
artikel
|
| 6 |
Design, synthesis and biological evaluation of 3-benzyloxy-linked pyrimidinylphenylamine derivatives as potent HIV-1 NNRTIs
|
Rai, Diwakar
|
|
2013
|
21 |
23 |
p. 7398-7405
8 p.
|
artikel
|
| 7 |
Design, synthesis and evaluation of novel 4-dimethylamine flavonoid derivatives as potential multi-functional anti-Alzheimer agents
|
Luo, Wen
|
|
2013
|
21 |
23 |
p. 7275-7282
8 p.
|
artikel
|
| 8 |
Development of fluorinated CB2 receptor agonists for PET studies
|
Lueg, Corinna
|
|
2013
|
21 |
23 |
p. 7481-7498
18 p.
|
artikel
|
| 9 |
1,3-Dialkyl-substituted tetrahydropyrimido[1,2-f]purine-2,4-diones as multiple target drugs for the potential treatment of neurodegenerative diseases
|
Koch, Pierre
|
|
2013
|
21 |
23 |
p. 7435-7452
18 p.
|
artikel
|
| 10 |
Dimethylaminopyridine derivatives of lupane triterpenoids cause mitochondrial disruption and induce the permeability transition
|
Bernardo, Telma C.
|
|
2013
|
21 |
23 |
p. 7239-7249
11 p.
|
artikel
|
| 11 |
Discovery and optimization of pyrrolo[1,2-a]pyrazinones leads to novel and selective inhibitors of PIM kinases
|
Casuscelli, Francesco
|
|
2013
|
21 |
23 |
p. 7364-7380
17 p.
|
artikel
|
| 12 |
Editorial board
|
|
|
2013
|
21 |
23 |
p. IFC-
1 p.
|
artikel
|
| 13 |
17(E)-Picolinylidene androstane derivatives as potential inhibitors of prostate cancer cell growth: Antiproliferative activity and molecular docking studies
|
Ajduković, Jovana J.
|
|
2013
|
21 |
23 |
p. 7257-7266
10 p.
|
artikel
|
| 14 |
Exploring a potential palonosetron allosteric binding site in the 5-HT3 receptor
|
Del Cadia, Marta
|
|
2013
|
21 |
23 |
p. 7523-7528
6 p.
|
artikel
|
| 15 |
Graphical contents list
|
|
|
2013
|
21 |
23 |
p. 7231-7238
8 p.
|
artikel
|
| 16 |
Inhibition of cholinesterase and monoamine oxidase-B activity by Tacrine–Homoisoflavonoid hybrids
|
Sun, Yang
|
|
2013
|
21 |
23 |
p. 7406-7417
12 p.
|
artikel
|
| 17 |
Ligand modifications to reduce the relative resistance of multi-drug resistant HIV-1 protease
|
Dewdney, Tamaria G.
|
|
2013
|
21 |
23 |
p. 7430-7434
5 p.
|
artikel
|
| 18 |
Peptide conjugates of 4-aminocyclophosphamide as prodrugs of phosphoramide mustard for selective activation by prostate-specific antigen (PSA)
|
Jiang, Yongying
|
|
2013
|
21 |
23 |
p. 7507-7514
8 p.
|
artikel
|
| 19 |
Small molecule fusion inhibitors: Design, synthesis and biological evaluation of (Z)-3-(5-(3-benzyl-4-oxo-2-thioxothiazolidinylidene)methyl)-N-(3-carboxy-4-hydroxy)phenyl-2,5-dimethylpyrroles and related derivatives targeting HIV-1 gp41
|
He, Xiao-Yang
|
|
2013
|
21 |
23 |
p. 7539-7548
10 p.
|
artikel
|
| 20 |
Synthesis and antimicrobial profile of N-substituted imidazolium oximes and their monoquaternary salts against multidrug resistant bacteria
|
Odžak, Renata
|
|
2013
|
21 |
23 |
p. 7499-7506
8 p.
|
artikel
|
| 21 |
Synthesis and biochemical evaluation of highly enantiomerically pure (R,R)- and (S,S)-alexidine
|
Gröst, Corinna
|
|
2013
|
21 |
23 |
p. 7357-7363
7 p.
|
artikel
|
| 22 |
Synthesis and biological evaluation of pyrrolidine-2-carbonitrile and 4-fluoropyrrolidine-2-carbonitrile derivatives as dipeptidyl peptidase-4 inhibitors for the treatment of type 2 diabetes
|
Wang, Jiang
|
|
2013
|
21 |
23 |
p. 7418-7429
12 p.
|
artikel
|
| 23 |
Synthesis and evaluation of the antimalarial, anticancer, and caspase 3 activities of tetraoxane dimers
|
Amewu, Richard K.
|
|
2013
|
21 |
23 |
p. 7392-7397
6 p.
|
artikel
|
| 24 |
Synthesis of combretastatin A-4 O-alkyl derivatives and evaluation of their cytotoxic, antiangiogenic and antitelomerase activity
|
Torijano-Gutiérrez, Sandra
|
|
2013
|
21 |
23 |
p. 7267-7274
8 p.
|
artikel
|
| 25 |
Synthesis, structure elucidation and in vitro anticancer activities of novel derivatives of diethyl (2E)-2-[(2E)-(1-arylimidazolidin-2-ylidene)hydrazono]succinate and ethyl (4-oxo-8-aryl-4,6,7,8-tetrahydroimidazo[2,1-c][1,2,4]triazin-3-yl)acetate
|
Sztanke, Małgorzata
|
|
2013
|
21 |
23 |
p. 7465-7480
16 p.
|
artikel
|
| 26 |
The 3,7-diazabicyclo[3.3.1]nonane scaffold for subtype selective nicotinic acetylcholine receptor ligands. Part 2: Carboxamide derivatives with different spacer motifs
|
Eibl, Christoph
|
|
2013
|
21 |
23 |
p. 7309-7329
21 p.
|
artikel
|
| 27 |
The 3,7-diazabicyclo[3.3.1]nonane scaffold for subtype selective nicotinic acetylcholine receptor (nAChR) ligands. Part 1: The influence of different hydrogen bond acceptor systems on alkyl and (hetero)aryl substituents
|
Eibl, Christoph
|
|
2013
|
21 |
23 |
p. 7283-7308
26 p.
|
artikel
|
| 28 |
The effect of pyridyl substituents on the thermodynamics of porphyrin binding to G-quadruplex DNA
|
Rowland, Gerald B.
|
|
2013
|
21 |
23 |
p. 7515-7522
8 p.
|
artikel
|
| 29 |
Trisubstituted and tetrasubstituted pyrazolines as a novel class of cell-growth inhibitors in tumor cells with wild type p53
|
Abdel-Halim, Mohammad
|
|
2013
|
21 |
23 |
p. 7343-7356
14 p.
|
artikel
|
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