| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Antimalarial acridines: Synthesis, in vitro activity against P. falciparum and interaction with hematin
|
Guetzoyan, Lucie
|
|
2009
|
17 |
23 |
p. 8032-8039
8 p.
|
artikel
|
| 2 |
Antimalarial activities of ferroquine conjugates with either glutathione reductase inhibitors or glutathione depletors via a hydrolyzable amide linker
|
Chavain, Natascha
|
|
2009
|
17 |
23 |
p. 8048-8059
12 p.
|
artikel
|
| 3 |
Antiprotozoal, anticancer and antimicrobial activities of dihydroartemisinin acetal dimers and monomers
|
Slade, Desmond
|
|
2009
|
17 |
23 |
p. 7949-7957
9 p.
|
artikel
|
| 4 |
Antitumor activity of diethynylfluorene derivatives of gold(I)
|
Chui, Chung-Hin
|
|
2009
|
17 |
23 |
p. 7872-7877
6 p.
|
artikel
|
| 5 |
Antitumor antibiotic fostriecin covalently binds to cysteine-269 residue of protein phosphatase 2A catalytic subunit in mammalian cells
|
Takeuchi, Toshifumi
|
|
2009
|
17 |
23 |
p. 8113-8122
10 p.
|
artikel
|
| 6 |
4-(3-Aryloxyaryl)quinoline alcohols are liver X receptor agonists
|
Bernotas, Ronald C.
|
|
2009
|
17 |
23 |
p. 8086-8092
7 p.
|
artikel
|
| 7 |
Bioorganic synthesis of a recombinant HIV-1 fusion inhibitor, SC35EK, with an N-terminal pyroglutamate capping group
|
Kajiwara, Kazumi
|
|
2009
|
17 |
23 |
p. 7964-7970
7 p.
|
artikel
|
| 8 |
Cytotoxicity mechanisms of pyrazino[1,2-b]isoquinoline-4-ones and SAR studies
|
Ortín, Irene
|
|
2009
|
17 |
23 |
p. 8040-8047
8 p.
|
artikel
|
| 9 |
Design and synthesis of N 6-substituted-4′-thioadenosine-5′-uronamides as potent and selective human A3 adenosine receptor agonists
|
Choi, Won Jun
|
|
2009
|
17 |
23 |
p. 8003-8011
9 p.
|
artikel
|
| 10 |
Development and characterization of lysine based tripeptide analogues as inhibitors of Sir2 activity
|
Chakrabarty, Subhra Prakash
|
|
2009
|
17 |
23 |
p. 8060-8072
13 p.
|
artikel
|
| 11 |
Discovery of benzo[g]indol-3-carboxylates as potent inhibitors of microsomal prostaglandin E2 synthase-1
|
Koeberle, Andreas
|
|
2009
|
17 |
23 |
p. 7924-7932
9 p.
|
artikel
|
| 12 |
Discovery of novel thieno[2,3-d]pyrimidin-4-yl hydrazone-based inhibitors of Cyclin D1-CDK4: Synthesis, biological evaluation and structure–activity relationships. Part 2
|
Horiuchi, Takao
|
|
2009
|
17 |
23 |
p. 7850-7860
11 p.
|
artikel
|
| 13 |
Editorial board
|
|
|
2009
|
17 |
23 |
p. IFC-
1 p.
|
artikel
|
| 14 |
Graphical contents list
|
|
|
2009
|
17 |
23 |
p. 7841-7849
9 p.
|
artikel
|
| 15 |
Insights into the physiological role of pig liver esterase: Isoenzymes show differences in the demethylation of prenylated proteins
|
Brüsehaber, Elke
|
|
2009
|
17 |
23 |
p. 7878-7883
6 p.
|
artikel
|
| 16 |
N-Acylpolyamine inhibitors of HDM2 and HDMX binding to p53
|
Hayashi, Ryo
|
|
2009
|
17 |
23 |
p. 7884-7893
10 p.
|
artikel
|
| 17 |
Natural and synthetic 2′-hydroxy-chalcones and aurones: Synthesis, characterization and evaluation of the antioxidant and soybean lipoxygenase inhibitory activity
|
Detsi, Anastasia
|
|
2009
|
17 |
23 |
p. 8073-8085
13 p.
|
artikel
|
| 18 |
Novel estrogen receptor (ER) modulators: Carbamate and thiocarbamate derivatives with m-carborane bisphenol structure
|
Ohta, Kiminori
|
|
2009
|
17 |
23 |
p. 7958-7963
6 p.
|
artikel
|
| 19 |
Novel O-[11C]methylated derivatives of candesartan as angiotensin II AT1 receptor imaging ligands: Radiosynthesis and ex vivo evaluation in rats
|
Hadizad, Tayebeh
|
|
2009
|
17 |
23 |
p. 7971-7977
7 p.
|
artikel
|
| 20 |
Oxidatively induced Cu for Mn exchange in protein phosphatase 1γ: A new method for active site analysis
|
Miyazaki, Atsushi
|
|
2009
|
17 |
23 |
p. 7978-7986
9 p.
|
artikel
|
| 21 |
Side chain azasteroids and thiasteroids as sterol methyltransferase inhibitors in ergosterol biosynthesis
|
Renard, Delphine
|
|
2009
|
17 |
23 |
p. 8123-8137
15 p.
|
artikel
|
| 22 |
Spare interactions of highly potent [Arg14,Lys15]nociceptin for cooperative induction of ORL1 receptor activation
|
Isozaki, Kaname
|
|
2009
|
17 |
23 |
p. 7904-7908
5 p.
|
artikel
|
| 23 |
Structural basis of the selectivity of the β2-adrenergic receptor for fluorinated catecholamines
|
Pooput, Chaya
|
|
2009
|
17 |
23 |
p. 7987-7992
6 p.
|
artikel
|
| 24 |
Structural optimization of a CXCR2-directed antagonist that indirectly inhibits γ-secretase and reduces Aβ
|
Bakshi, Pancham
|
|
2009
|
17 |
23 |
p. 8102-8112
11 p.
|
artikel
|
| 25 |
Synthesis and biological evaluation of the metabolites of 2-(1-{3-[(6-chloronaphthalen-2-yl)sulfonyl]propanoyl}piperidin-4-yl)-5-methyl-1,2-dihydro-3H-imidazo[1,5-c]imidazol-3-one
|
Fujimoto, Takuya
|
|
2009
|
17 |
23 |
p. 7993-8002
10 p.
|
artikel
|
| 26 |
Synthesis and biological evaluation of 3′,4′,5′-trimethoxychalcone analogues as inhibitors of nitric oxide production and tumor cell proliferation
|
Rao, Yerra Koteswara
|
|
2009
|
17 |
23 |
p. 7909-7914
6 p.
|
artikel
|
| 27 |
Synthesis and HMG-CoA reductase inhibition of 2-cyclopropyl-4-thiophenyl-quinoline mevalonolactones
|
Zhao, Shikui
|
|
2009
|
17 |
23 |
p. 7915-7923
9 p.
|
artikel
|
| 28 |
Synthesis, antibacterial activities and molecular docking studies of peptide and Schiff bases as targeted antibiotics
|
Cheng, Kui
|
|
2009
|
17 |
23 |
p. 7861-7871
11 p.
|
artikel
|
| 29 |
Synthesis of 4-thiophen-2′-yl-1,4-dihydropyridines as potentiators of the CFTR chloride channel
|
Cateni, Francesca
|
|
2009
|
17 |
23 |
p. 7894-7903
10 p.
|
artikel
|
| 30 |
Synthesis, tautomerism, and antimicrobial, anti-HCV, anti-SSPE, antioxidant, and antitumor activities of arylazobenzosuberones
|
Farghaly, Thoraya A.
|
|
2009
|
17 |
23 |
p. 8012-8019
8 p.
|
artikel
|
| 31 |
Theoretical calculations of a model of NOS indazole inhibitors: Interaction of aromatic compounds with Zn-porphyrins
|
Elguero, José
|
|
2009
|
17 |
23 |
p. 8027-8031
5 p.
|
artikel
|
| 32 |
The selective quantification of iron by hexadentate fluorescent probes
|
Ma, Yong Min
|
|
2009
|
17 |
23 |
p. 8093-8101
9 p.
|
artikel
|
| 33 |
The spirocyclopropyl moiety as a methyl surrogate in the structure of l-fucosidase and l-rhamnosidase inhibitors
|
Pearson, Morwenna S.M.
|
|
2009
|
17 |
23 |
p. 8020-8026
7 p.
|
artikel
|
| 34 |
5-Vinyl-3-pyridinecarbonitrile inhibitors of PKCθ: Optimization of enzymatic and functional activity
|
Tumey, L. Nathan
|
|
2009
|
17 |
23 |
p. 7933-7948
16 p.
|
artikel
|
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