| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Amide-containing diketoacids as HIV-1 integrase inhibitors: Synthesis, structure–activity relationship analysis, and biological activity
|
Li, Hongcai
|
|
2009
|
17 |
7 |
p. 2913-2919
7 p.
|
artikel
|
| 2 |
Antiproliferative and antimalarial anthraquinones of Scutia myrtina from the Madagascar forest
|
Hou, Yanpeng
|
|
2009
|
17 |
7 |
p. 2871-2876
6 p.
|
artikel
|
| 3 |
Argifin; efficient solid phase total synthesis and evalution of analogues of acyclic peptide
|
Sunazuka, Toshiaki
|
|
2009
|
17 |
7 |
p. 2751-2758
8 p.
|
artikel
|
| 4 |
Binary and ternary inclusion complexes of finasteride in HPβCD and polymers: Preparation and characterization
|
Asbahr, Ana Carolina C.
|
|
2009
|
17 |
7 |
p. 2718-2723
6 p.
|
artikel
|
| 5 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2009
|
17 |
7 |
p. 2937-2939
3 p.
|
artikel
|
| 6 |
8-Bromo-9-alkyl adenine derivatives as tools for developing new adenosine A2A and A2B receptors ligands
|
Lambertucci, Catia
|
|
2009
|
17 |
7 |
p. 2812-2822
11 p.
|
artikel
|
| 7 |
Carbonic anhydrase inhibitors. Inhibition of the β-class enzymes from the fungal pathogens Candida albicans and Cryptococcus neoformans with aliphatic and aromatic carboxylates
|
Innocenti, Alessio
|
|
2009
|
17 |
7 |
p. 2654-2657
4 p.
|
artikel
|
| 8 |
Characteristic of neuraminidase inhibitory xanthones from Cudrania tricuspidata
|
Ryu, Young Bae
|
|
2009
|
17 |
7 |
p. 2744-2750
7 p.
|
artikel
|
| 9 |
Design and synthesis of novel dihydroquinoline-3-carboxylic acids as HIV-1 integrase inhibitors
|
Sechi, Mario
|
|
2009
|
17 |
7 |
p. 2925-2935
11 p.
|
artikel
|
| 10 |
Design, synthesis and SAR studies of tripeptide analogs with the scaffold 3-phenylpropane-1,2-diamine as aminopeptidase N/CD13 inhibitors
|
Shang, Luqing
|
|
2009
|
17 |
7 |
p. 2775-2784
10 p.
|
artikel
|
| 11 |
Design, synthesis, biological evaluation and molecular modelling studies of novel quinoline derivatives against Mycobacterium tuberculosis
|
Upadhayaya, Ram Shankar
|
|
2009
|
17 |
7 |
p. 2830-2841
12 p.
|
artikel
|
| 12 |
Discovery and structure–activity relationships of (2-(arylthio)benzylideneamino)guanidines as a novel series of potent apoptosis inducers
|
Zhang, Han-Zhong
|
|
2009
|
17 |
7 |
p. 2852-2858
7 p.
|
artikel
|
| 13 |
Discovery of 2-(5-nitrothiazol-2-ylthio)benzo[d]thiazoles as novel c-Jun N-terminal kinase inhibitors
|
De, Surya K.
|
|
2009
|
17 |
7 |
p. 2712-2717
6 p.
|
artikel
|
| 14 |
Discovery of potent and orally active 3-alkoxy-5-phenoxy-N-thiazolyl benzamides as novel allosteric glucokinase activators
|
Iino, Tomoharu
|
|
2009
|
17 |
7 |
p. 2733-2743
11 p.
|
artikel
|
| 15 |
Editorial board
|
|
|
2009
|
17 |
7 |
p. IFC-
1 p.
|
artikel
|
| 16 |
Erratum to “Search for new pharmacophores for antimalarial activity. Part I: Synthesis and antimalarial activity of new 2-methyl-6-ureido-4-quinolinamides” [Bioorg. Med. Chem. 17 (2009) 203–221]
|
Madapa, S.
|
|
2009
|
17 |
7 |
p. 2936-
1 p.
|
artikel
|
| 17 |
Fluorinated isatin derivatives. Part 1: Synthesis of new N-substituted (S)-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatins as potent caspase-3 and -7 inhibitors
|
Podichetty, Anil Kumar
|
|
2009
|
17 |
7 |
p. 2680-2688
9 p.
|
artikel
|
| 18 |
Graphical contents list
|
|
|
2009
|
17 |
7 |
p. 2635-2644
10 p.
|
artikel
|
| 19 |
IKKβ inhibitors identification part I: Homology model assisted structure based virtual screening
|
Nagarajan, Shanthi
|
|
2009
|
17 |
7 |
p. 2759-2766
8 p.
|
artikel
|
| 20 |
Incorporation of an inducible nucleotide analog into DNA by DNA polymerases
|
Ali, Md. Monsur
|
|
2009
|
17 |
7 |
p. 2859-2863
5 p.
|
artikel
|
| 21 |
Instructions to contributors
|
|
|
2009
|
17 |
7 |
p. I-
1 p.
|
artikel
|
| 22 |
Modified low molecular weight cyclic peptides as mimetics of BDNF with improved potency, proteolytic stability and transmembrane passage in vitro
|
Fletcher, Jordan M.
|
|
2009
|
17 |
7 |
p. 2695-2702
8 p.
|
artikel
|
| 23 |
Molecular modeling studies and in vitro bioactivity evaluation of a set of novel 5-nitro-heterocyclic derivatives as anti-T. cruzi agents
|
Paula, Fávero Reisdorfer
|
|
2009
|
17 |
7 |
p. 2673-2679
7 p.
|
artikel
|
| 24 |
New pyridazine derivatives: Synthesis, chemistry and biological activity
|
Butnariu, Roxana M.
|
|
2009
|
17 |
7 |
p. 2823-2829
7 p.
|
artikel
|
| 25 |
Partial regeneration of β-cells in the islets of Langerhans by Nymphayol a sterol isolated from Nymphaea stellata (Willd.) flowers
|
Subash-Babu, P.
|
|
2009
|
17 |
7 |
p. 2864-2870
7 p.
|
artikel
|
| 26 |
Phenolic compounds with radical scavenging and cyclooxygenase-2 (COX-2) inhibitory activities from Dioscorea opposita
|
Yang, Min Hye
|
|
2009
|
17 |
7 |
p. 2689-2694
6 p.
|
artikel
|
| 27 |
Probing of the cis-5-phenyl proline scaffold as a platform for the synthesis of mechanism-based inhibitors of the Staphylococcus aureus sortase SrtA isoform
|
Kudryavtsev, Konstantin V.
|
|
2009
|
17 |
7 |
p. 2886-2893
8 p.
|
artikel
|
| 28 |
Selectivity profiling of DegP substrates and inhibitors
|
Hauske, Patrick
|
|
2009
|
17 |
7 |
p. 2920-2924
5 p.
|
artikel
|
| 29 |
Sesquiterpene-like inhibitors of a 9-cis-epoxycarotenoid dioxygenase regulating abscisic acid biosynthesis in higher plants
|
Boyd, Jason
|
|
2009
|
17 |
7 |
p. 2902-2912
11 p.
|
artikel
|
| 30 |
Solution studies on the complex of 4′-epiadriamycin-d-(CGATCG)2 followed by time-resolved fluorescence measurement, diffusion ordered spectroscopy and restrained molecular dynamics simulations
|
Agrawal, Prashansa
|
|
2009
|
17 |
7 |
p. 2793-2811
19 p.
|
artikel
|
| 31 |
Studies on quinones. Part 45: Novel 7-aminoisoquinoline-5,8-quinone derivatives with antitumor properties on cancer cell lines
|
Valderrama, Jaime A.
|
|
2009
|
17 |
7 |
p. 2894-2901
8 p.
|
artikel
|
| 32 |
12-Substituted 2,3-dimethoxy-8,9-methylenedioxybenzo[i]phenanthridines as novel topoisomerase I-targeting antitumor agents
|
Feng, Wei
|
|
2009
|
17 |
7 |
p. 2877-2885
9 p.
|
artikel
|
| 33 |
Synthesis, activity and molecular modeling of a new series of chromones as low molecular weight protein tyrosine phosphatase inhibitors
|
Forghieri, Marco
|
|
2009
|
17 |
7 |
p. 2658-2672
15 p.
|
artikel
|
| 34 |
Synthesis and biological evaluation of N 4-(hetero)arylsulfonylquinoxalinones as HIV-1 reverse transcriptase inhibitors
|
Xu, Bailing
|
|
2009
|
17 |
7 |
p. 2767-2774
8 p.
|
artikel
|
| 35 |
Synthesis and evaluation of myxochelin analogues as antimetastatic agents
|
Miyanaga, Satoshi
|
|
2009
|
17 |
7 |
p. 2724-2732
9 p.
|
artikel
|
| 36 |
Synthesis and pharmacological evaluation of coumarin derivatives as cannabinoid receptor antagonists and inverse agonists
|
Behrenswerth, Andrea
|
|
2009
|
17 |
7 |
p. 2842-2851
10 p.
|
artikel
|
| 37 |
Synthesis, anti-inflammatory, and antioxidant activities of 18β-glycyrrhetinic acid derivatives as chemical mediators and xanthine oxidase inhibitors
|
Maitraie, Dravidum
|
|
2009
|
17 |
7 |
p. 2785-2792
8 p.
|
artikel
|
| 38 |
The effect of individual N-glycans on enzyme activity
|
Skropeta, Danielle
|
|
2009
|
17 |
7 |
p. 2645-2653
9 p.
|
artikel
|
| 39 |
Thiodisaccharides with galactofuranose or arabinofuranose as terminal units: Synthesis and inhibitory activity of an exo β-d-galactofuranosidase
|
Repetto, Evangelina
|
|
2009
|
17 |
7 |
p. 2703-2711
9 p.
|
artikel
|
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