| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Antiviral activity of seed extract from Citrus bergamia towards human retroviruses
|
Balestrieri, Emanuela
|
|
2011
|
19 |
6 |
p. 2084-2089
6 p.
|
artikel
|
| 2 |
A rational approach for the design and synthesis of 1-acetyl-3,5-diaryl-4,5-dihydro(1H)pyrazoles as a new class of potential non-purine xanthine oxidase inhibitors
|
Nepali, Kunal
|
|
2011
|
19 |
6 |
p. 1950-1958
9 p.
|
artikel
|
| 3 |
CD22-Antagonists with nanomolar potency: The synergistic effect of hydrophobic groups at C-2 and C-9 of sialic acid scaffold
|
Abdu-Allah, Hajjaj H.M.
|
|
2011
|
19 |
6 |
p. 1966-1971
6 p.
|
artikel
|
| 4 |
Design, synthesis and antitumor evaluation of phenyl N-mustard-quinazoline conjugates
|
Marvania, Bhavin
|
|
2011
|
19 |
6 |
p. 1987-1998
12 p.
|
artikel
|
| 5 |
Design, synthesis and docking study of 5-amino substituted indeno[1,2-c]isoquinolines as novel topoisomerase I inhibitors
|
Khadka, Daulat Bikram
|
|
2011
|
19 |
6 |
p. 1924-1929
6 p.
|
artikel
|
| 6 |
Development of sulfonamide AKT PH domain inhibitors
|
Ahad, Ali Md.
|
|
2011
|
19 |
6 |
p. 2046-2054
9 p.
|
artikel
|
| 7 |
Discovery of a new 2-aminobenzhydrol template for highly potent squalene synthase inhibitors
|
Ichikawa, Masanori
|
|
2011
|
19 |
6 |
p. 1930-1949
20 p.
|
artikel
|
| 8 |
Editorial board
|
|
|
2011
|
19 |
6 |
p. IFC-
1 p.
|
artikel
|
| 9 |
Effect of structural modification in the amine portion of substituted aminobutyl-benzamides as ligands for binding σ1 and σ2 receptors
|
Fan, Kuo-Hsien
|
|
2011
|
19 |
6 |
p. 1852-1859
8 p.
|
artikel
|
| 10 |
Ferrocenyl chalcones versus organic chalcones: A comparative study of their nematocidal activity
|
Attar, Saeed
|
|
2011
|
19 |
6 |
p. 2055-2073
19 p.
|
artikel
|
| 11 |
Further SAR study on 11-O-substituted aporphine analogues: Identification of highly potent dopamine D3 receptor ligands
|
Ye, Na
|
|
2011
|
19 |
6 |
p. 1999-2008
10 p.
|
artikel
|
| 12 |
Graphical contents list
|
|
|
2011
|
19 |
6 |
p. 1839-1846
8 p.
|
artikel
|
| 13 |
Involvement of heme oxygenase-1 induction via Nrf2/ARE activation in protection against H2O2-induced PC12 cell death by a metabolite of sesamin contained in sesame seeds
|
Hamada, Nanako
|
|
2011
|
19 |
6 |
p. 1959-1965
7 p.
|
artikel
|
| 14 |
Isolation, structure identification and SAR studies on thiosugar sulfonium salts, neosalaprinol and neoponkoranol, as potent α-glucosidase inhibitors
|
Xie, Weijia
|
|
2011
|
19 |
6 |
p. 2015-2022
8 p.
|
artikel
|
| 15 |
MMT, Npeoc-protected spermine, a valuable synthon for the solid phase synthesis of oligonucleotide oligospermine conjugates via guanidine linkers
|
Perche, Phanélie
|
|
2011
|
19 |
6 |
p. 1972-1977
6 p.
|
artikel
|
| 16 |
New bichalcone analogs as NF-κB inhibitors and as cytotoxic agents inducing Fas/CD95-dependent apoptosis
|
Reddy, M. Vijaya Bhaskar
|
|
2011
|
19 |
6 |
p. 1895-1906
12 p.
|
artikel
|
| 17 |
Novel and potent calcium-sensing receptor antagonists: Discovery of (5R)-N-[1-ethyl-1-(4-ethylphenyl)propyl]-2,7,7-trimethyl-5-phenyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxamide monotosylate (TAK-075) as an orally active bone anabolic agent
|
Yoshida, Masato
|
|
2011
|
19 |
6 |
p. 1881-1894
14 p.
|
artikel
|
| 18 |
Parallel solid-phase synthesis of a small library of linear and hydrocarbon-bridged analogues of VEGF81–91: Potential biological tools for studying the VEGF/VEGFR-1 interaction
|
García-Aranda, María Isabel
|
|
2011
|
19 |
6 |
p. 1978-1986
9 p.
|
artikel
|
| 19 |
Purification and inhibition studies with anions and sulfonamides of an α-carbonic anhydrase from the Antarctic seal Leptonychotes weddellii
|
Cincinelli, Alessandra
|
|
2011
|
19 |
6 |
p. 1847-1851
5 p.
|
artikel
|
| 20 |
Structure–activity relationships of flavonoids as inhibitors of breast cancer resistance protein (BCRP)
|
Pick, Anne
|
|
2011
|
19 |
6 |
p. 2090-2102
13 p.
|
artikel
|
| 21 |
Structure–activity relationships of hypervalent organochalcogenanes as inhibitors of cysteine cathepsins V and S
|
Piovan, Leandro
|
|
2011
|
19 |
6 |
p. 2009-2014
6 p.
|
artikel
|
| 22 |
Structure based design and syntheses of amino-1H-pyrazole amide derivatives as selective Raf kinase inhibitors in melanoma cells
|
Kim, Mi-hyun
|
|
2011
|
19 |
6 |
p. 1915-1923
9 p.
|
artikel
|
| 23 |
Syntheses and characterization of nimesulide derivatives for dual enzyme inhibitors of both cyclooxygenase-1/2 and 5-lipoxygenase
|
Li, Yue
|
|
2011
|
19 |
6 |
p. 2074-2083
10 p.
|
artikel
|
| 24 |
Synthesis and anti-HSV-1 activity of new 1,2,3-triazole derivatives
|
Jordão, Alessandro K.
|
|
2011
|
19 |
6 |
p. 1860-1865
6 p.
|
artikel
|
| 25 |
Synthesis and biological evaluation of benzimidazole-5-carbohydrazide derivatives as antimalarial, cytotoxic and antitubercular agents
|
Camacho, José
|
|
2011
|
19 |
6 |
p. 2023-2029
7 p.
|
artikel
|
| 26 |
Synthesis and biological evaluation of l-valine-amidoximeesters as double prodrugs of amidines
|
Kotthaus, Joscha
|
|
2011
|
19 |
6 |
p. 1907-1914
8 p.
|
artikel
|
| 27 |
Synthesis, biological evaluation and 3D-QSAR studies of 3-keto salicylic acid chalcones and related amides as novel HIV-1 integrase inhibitors
|
Sharma, Horrick
|
|
2011
|
19 |
6 |
p. 2030-2045
16 p.
|
artikel
|
| 28 |
Synthesis of new glycyrrhetinic acid derived ring A azepanone, 29-urea and 29-hydroxamic acid derivatives as selective 11β-hydroxysteroid dehydrogenase 2 inhibitors
|
Gaware, Rawindra
|
|
2011
|
19 |
6 |
p. 1866-1880
15 p.
|
artikel
|
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