| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Anion inhibition studies of the α-carbonic anhydrase from the protozoan pathogen Trypanosoma cruzi, the causative agent of Chagas disease
|
Pan, Peiwen
|
|
2013
|
21 |
15 |
p. 4472-4476
5 p.
|
artikel
|
| 2 |
Anticancer activity and SAR studies of substituted 1,4-naphthoquinones
|
Bhasin, Deepak
|
|
2013
|
21 |
15 |
p. 4662-4669
8 p.
|
artikel
|
| 3 |
Chemically modified siRNAs and miRNAs bearing urea/thiourea-bridged aromatic compounds at their 3′-end for RNAi therapy
|
Kitamura, Yoshiaki
|
|
2013
|
21 |
15 |
p. 4494-4501
8 p.
|
artikel
|
| 4 |
Control of the intracellular levels of prostaglandin E2 through inhibition of the 15-hydroxyprostaglandin dehydrogenase for wound healing
|
Choi, Dubok
|
|
2013
|
21 |
15 |
p. 4477-4484
8 p.
|
artikel
|
| 5 |
Design and synthesis of N-alkyl-N′-substituted 2,4-dioxo-3,4-dihydropyrimidin-1-diacylhydrazine derivatives as ecdysone receptor agonist
|
Liu, Xiu
|
|
2013
|
21 |
15 |
p. 4687-4697
11 p.
|
artikel
|
| 6 |
Design, synthesis and evaluation of novel 2-hydroxypyrrolobenzodiazepine-5,11-dione analogues as potent angiotensin converting enzyme (ACE) inhibitors
|
Addla, Dinesh
|
|
2013
|
21 |
15 |
p. 4485-4493
9 p.
|
artikel
|
| 7 |
Design, synthesis, and evaluation of novel VEGFR2 kinase inhibitors: Discovery of [1,2,4]triazolo[1,5-a]pyridine derivatives with slow dissociation kinetics
|
Oguro, Yuya
|
|
2013
|
21 |
15 |
p. 4714-4729
16 p.
|
artikel
|
| 8 |
Design, synthesis and neuroprotective evaluation of novel tacrine–benzothiazole hybrids as multi-targeted compounds against Alzheimer’s disease
|
Keri, Rangappa S.
|
|
2013
|
21 |
15 |
p. 4559-4569
11 p.
|
artikel
|
| 9 |
Determination of the binding mode and interacting amino-acids for dibasic H3 receptor antagonists
|
Levoin, Nicolas
|
|
2013
|
21 |
15 |
p. 4526-4529
4 p.
|
artikel
|
| 10 |
Discovery of benzamide analogs as negative allosteric modulators of human neuronal nicotinic receptors: Pharmacophore modeling and structure–activity relationship studies
|
Yi, Bitna
|
|
2013
|
21 |
15 |
p. 4730-4743
14 p.
|
artikel
|
| 11 |
Editorial board
|
|
|
2013
|
21 |
15 |
p. IFC-
1 p.
|
artikel
|
| 12 |
Graphical contents list
|
|
|
2013
|
21 |
15 |
p. 4443-4451
9 p.
|
artikel
|
| 13 |
Indole derivatives as dual-effective agents for the treatment of neurodegenerative diseases: Synthesis, biological evaluation, and molecular modeling studies
|
Buemi, Maria Rosa
|
|
2013
|
21 |
15 |
p. 4575-4580
6 p.
|
artikel
|
| 14 |
In vitro antiviral activity of phlorotannins isolated from Ecklonia cava against porcine epidemic diarrhea coronavirus infection and hemagglutination
|
Kwon, Hyung-Jun
|
|
2013
|
21 |
15 |
p. 4706-4713
8 p.
|
artikel
|
| 15 |
Macrocyclic biphenyl tetraoxazoles: Synthesis, evaluation as G-quadruplex stabilizers and cytotoxic activity
|
Blankson, Gifty A.
|
|
2013
|
21 |
15 |
p. 4511-4520
10 p.
|
artikel
|
| 16 |
Metabolism of the phytoalexins camalexins, their bioisosteres and analogues in the plant pathogenic fungus Alternaria brassicicola
|
Pedras, M. Soledade C.
|
|
2013
|
21 |
15 |
p. 4541-4549
9 p.
|
artikel
|
| 17 |
Molecular docking guided structure based design of symmetrical N,N′-disubstituted urea/thiourea as HIV-1 gp120–CD4 binding inhibitors
|
Sivan, Sree Kanth
|
|
2013
|
21 |
15 |
p. 4591-4599
9 p.
|
artikel
|
| 18 |
Multimerized CHR-derived peptides as HIV-1 fusion inhibitors
|
Nomura, Wataru
|
|
2013
|
21 |
15 |
p. 4452-4458
7 p.
|
artikel
|
| 19 |
Novel chlorinated dibenzofurans isolated from the cellular slime mold, Polysphondylium filamentosum, and their biological activities
|
Kikuchi, Haruhisa
|
|
2013
|
21 |
15 |
p. 4628-4633
6 p.
|
artikel
|
| 20 |
Novel triple reuptake inhibitors with low risk of CAD associated liabilities: Design, synthesis and biological activities of 4-[(1S)-1-(3,4-dichlorophenyl)-2-methoxyethyl]piperidine and related compounds
|
Ishichi, Yuji
|
|
2013
|
21 |
15 |
p. 4600-4613
14 p.
|
artikel
|
| 21 |
3′-Oxo-, amino-, thio- and sulfone-acetic acid modified thymidines: Effect of increased acidity on ribonuclease A inhibition
|
Datta, Dhrubajyoti
|
|
2013
|
21 |
15 |
p. 4634-4645
12 p.
|
artikel
|
| 22 |
Promising anti-growth effects of palladium(II) saccharinate complex of terpyridine by inducing apoptosis on transformed fibroblasts in vitro
|
Coskun, Melis Debreli
|
|
2013
|
21 |
15 |
p. 4698-4705
8 p.
|
artikel
|
| 23 |
Protective activity of (1S,2E,4R,6R,7E,11E)-2,7,11-cembratriene-4,6-diol analogues against diisopropylfluorophosphate neurotoxicity: Preliminary structure–activity relationship and pharmacophore modeling
|
Eterović, Vesna A.
|
|
2013
|
21 |
15 |
p. 4678-4686
9 p.
|
artikel
|
| 24 |
Structure–activity-relationship studies on dihydrofuran-fused perhydrophenanthrenes as an anti-Alzheimer’s disease agent
|
Sugimoto, Kenji
|
|
2013
|
21 |
15 |
p. 4459-4471
13 p.
|
artikel
|
| 25 |
Substituents effects on activity of kynureninase from Homo sapiens and Pseudomonas fluorescens
|
Maitrani, Chandan
|
|
2013
|
21 |
15 |
p. 4670-4677
8 p.
|
artikel
|
| 26 |
7-Substituted-sulfocoumarins are isoform-selective, potent carbonic anhydrase II inhibitors
|
Tanc, Muhammet
|
|
2013
|
21 |
15 |
p. 4502-4510
9 p.
|
artikel
|
| 27 |
Synthesis and biological validation of N 7-(4-chlorophenoxyethyl) substituted dinucleotide cap analogs for mRNA translation
|
Kore, Anilkumar R.
|
|
2013
|
21 |
15 |
p. 4570-4574
5 p.
|
artikel
|
| 28 |
Synthesis and evaluation of N 8-acetylspermidine analogues as inhibitors of bacterial acetylpolyamine amidohydrolase
|
Decroos, Christophe
|
|
2013
|
21 |
15 |
p. 4530-4540
11 p.
|
artikel
|
| 29 |
Synthesis and in vitro evaluation of new ethyl and methyl quinoxaline-7-carboxylate 1,4-di-N-oxide against Entamoeba histolytica
|
Duque-Montaño, Blanca Estela
|
|
2013
|
21 |
15 |
p. 4550-4558
9 p.
|
artikel
|
| 30 |
Synthesis, biological evaluation, X-ray molecular structure and molecular docking studies of RGD mimetics containing 6-amino-2,3-dihydroisoindolin-1-one fragment as ligands of integrin αIIbβ3
|
Krysko, Andrei A.
|
|
2013
|
21 |
15 |
p. 4646-4661
16 p.
|
artikel
|
| 31 |
Synthesis of novel celecoxib analogues by bioisosteric replacement of sulfonamide as potent anti-inflammatory agents and cyclooxygenase inhibitors
|
Chandna, Nisha
|
|
2013
|
21 |
15 |
p. 4581-4590
10 p.
|
artikel
|
| 32 |
Synthesis of substituted diphenyl sulfones and their structure–activity relationship with the antagonism of 5-НТ6 receptors
|
Ivachtchenko, Alexandre
|
|
2013
|
21 |
15 |
p. 4614-4627
14 p.
|
artikel
|
| 33 |
The extremo-α-carbonic anhydrase from the thermophilic bacterium Sulfurihydrogenibium azorense is highly inhibited by sulfonamides
|
Vullo, Daniela
|
|
2013
|
21 |
15 |
p. 4521-4525
5 p.
|
artikel
|
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