nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A novel Syk family kinase inhibitor: Design, synthesis, and structure–activity relationship of 1,2,4-triazolo[4,3-c]pyrimidine and 1,2,4-triazolo[1,5-c]pyrimidine derivatives
|
Hirabayashi, Akihito |
|
2008 |
16 |
15 |
p. 7347-7357 11 p. |
artikel |
2 |
Anticonvulsant activity of some xanthone derivatives
|
Marona, Henryk |
|
2008 |
16 |
15 |
p. 7234-7244 11 p. |
artikel |
3 |
Aromatic 2-chloroethyl urea derivatives and bioisosteres. Part 2: Cytocidal activity and effects on the nuclear translocation of thioredoxin-1, and the cell cycle progression
|
Fortin, Jessica S. |
|
2008 |
16 |
15 |
p. 7477-7488 12 p. |
artikel |
4 |
Baicalin, a prodrug able to reach the CNS, is a prolyl oligopeptidase inhibitor
|
Tarragó, Teresa |
|
2008 |
16 |
15 |
p. 7516-7524 9 p. |
artikel |
5 |
Bis(sulfonamide) isosters of mycophenolic adenine dinucleotide analogues: Inhibition of inosine monophosphate dehydrogenase
|
Chen, Liqiang |
|
2008 |
16 |
15 |
p. 7462-7469 8 p. |
artikel |
6 |
Carbonic anhydrase inhibitors: Inhibition of mammalian isoforms I–XIV with a series of substituted phenols including paracetamol and salicylic acid
|
Innocenti, Alessio |
|
2008 |
16 |
15 |
p. 7424-7428 5 p. |
artikel |
7 |
Characterization of the PON1 active site using modeling simulation, in relation to PON1 lactonase activity
|
Tavori, Hagai |
|
2008 |
16 |
15 |
p. 7504-7509 6 p. |
artikel |
8 |
Cinnamoyl- and hydroxycinnamoyl amides of glaucine and their antioxidative and antiviral activities
|
Spasova, Maya |
|
2008 |
16 |
15 |
p. 7457-7461 5 p. |
artikel |
9 |
Comparative molecular dynamics simulations of the potent synthetic classical cannabinoid ligand AMG3 in solution and at binding site of the CB1 and CB2 receptors
|
Durdagi, Serdar |
|
2008 |
16 |
15 |
p. 7377-7387 11 p. |
artikel |
10 |
Design and synthesis of novel oxazole containing 1,3-Dioxane-2-carboxylic acid derivatives as PPAR α/γ dual agonists
|
Pingali, Harikishore |
|
2008 |
16 |
15 |
p. 7117-7127 11 p. |
artikel |
11 |
Design, synthesis, and biological evaluation of Mannich bases of heterocyclic chalcone analogs as cytotoxic agents
|
Reddy, M. Vijaya Bhaskar |
|
2008 |
16 |
15 |
p. 7358-7370 13 p. |
artikel |
12 |
Design, synthesis, and biological evaluation of pirenzepine analogs bearing a 1,2-cyclohexanediamine and perhydroquinoxaline units in exchange for the piperazine ring as antimuscarinics
|
Minarini, Anna |
|
2008 |
16 |
15 |
p. 7311-7320 10 p. |
artikel |
13 |
Design, synthesis, and evaluation of 3C protease inhibitors as anti-enterovirus 71 agents
|
Kuo, Chih-Jung |
|
2008 |
16 |
15 |
p. 7388-7398 11 p. |
artikel |
14 |
Discovery and stereoselective synthesis of the novel isochroman neurokinin-1 receptor antagonist ‘CJ-17,493’
|
Shishido, Yuji |
|
2008 |
16 |
15 |
p. 7193-7205 13 p. |
artikel |
15 |
Editorial board
|
|
|
2008 |
16 |
15 |
p. IFC- 1 p. |
artikel |
16 |
Enhanced affinity of ketotifen toward tamarind seed polysaccharide in comparison with hydroxyethylcellulose and hyaluronic acid: A nuclear magnetic resonance investigation
|
Uccello-Barretta, Gloria |
|
2008 |
16 |
15 |
p. 7371-7376 6 p. |
artikel |
17 |
Fluorinated phenylcyclopropylamines. Part 5: Effects of electron-withdrawing or -donating aryl substituents on the inhibition of monoamine oxidases A and B by 2-aryl-2-fluoro-cyclopropylamines
|
Hruschka, Svenja |
|
2008 |
16 |
15 |
p. 7148-7166 19 p. |
artikel |
18 |
Functionalized pyrrolidine inhibitors of human type II α-mannosidases as anti-cancer agents: Optimizing the fit to the active site
|
Fiaux, Hélène |
|
2008 |
16 |
15 |
p. 7337-7346 10 p. |
artikel |
19 |
Graphical contents list
|
|
|
2008 |
16 |
15 |
p. 7081-7094 14 p. |
artikel |
20 |
Hanultarin, a cytotoxic lignan as an inhibitor of actin cytoskeleton polymerization from the seeds of Trichosanthes kirilowii
|
Moon, Surk-Sik |
|
2008 |
16 |
15 |
p. 7264-7269 6 p. |
artikel |
21 |
Homo- and hetero-bivalent edrophonium-like ammonium salts as highly potent, dual binding site AChE inhibitors
|
Leonetti, Francesco |
|
2008 |
16 |
15 |
p. 7450-7456 7 p. |
artikel |
22 |
Identification of a butyrophenone analog as a potential atypical antipsychotic agent: 4-[4-(4-Chlorophenyl)-1,4-diazepan-1-yl]-1-(4-fluorophenyl)butan-1-one
|
Ablordeppey, Seth Y. |
|
2008 |
16 |
15 |
p. 7291-7301 11 p. |
artikel |
23 |
Identification of a methotrexate-binding peptide from a T7 phage display screen using a QCM device
|
Takakusagi, Yoichi |
|
2008 |
16 |
15 |
p. 7410-7414 5 p. |
artikel |
24 |
Illudalic acid as a potential LAR inhibitor: Synthesis, SAR, and preliminary studies on the mechanism of action
|
Ling, Qing |
|
2008 |
16 |
15 |
p. 7399-7409 11 p. |
artikel |
25 |
Instructions to contributors
|
|
|
2008 |
16 |
15 |
p. I- 1 p. |
artikel |
26 |
In vitro inhibition of glycogen-degrading enzymes and glycosidases by six-membered sugar mimics and their evaluation in cell cultures
|
Kuriyama, Chinami |
|
2008 |
16 |
15 |
p. 7330-7336 7 p. |
artikel |
27 |
Lack of aquaporin-4 water transport inhibition by antiepileptics and arylsulfonamides
|
Yang, Baoxue |
|
2008 |
16 |
15 |
p. 7489-7493 5 p. |
artikel |
28 |
Major sperm protein as a diagnostic antigen for onchocerciasis
|
Park, Junguk |
|
2008 |
16 |
15 |
p. 7206-7209 4 p. |
artikel |
29 |
Molecular features of the prazosin molecule required for activation of Transport-P
|
da Silva, Joaquim Fernando Mendes |
|
2008 |
16 |
15 |
p. 7254-7263 10 p. |
artikel |
30 |
Muscarinic receptor 1 agonist activity of novel N-arylthioureas substituted 3-morpholino arecoline derivatives in Alzheimer’s presenile dementia models
|
Malviya, Manish |
|
2008 |
16 |
15 |
p. 7095-7101 7 p. |
artikel |
31 |
Nitrogen-containing flavonoid analogues as CDK1/cyclin B inhibitors: Synthesis, SAR analysis, and biological activity
|
Zhang, Shixuan |
|
2008 |
16 |
15 |
p. 7127-7132 6 p. |
artikel |
32 |
Novel inhibitors of anthrax edema factor
|
Chen, Deliang |
|
2008 |
16 |
15 |
p. 7225-7233 9 p. |
artikel |
33 |
Novel N1-substituted 1,3-dihydro-2H-benzimidazol-2-ones as potent non-nucleoside reverse transcriptase inhibitors
|
Monforte, Anna-Maria |
|
2008 |
16 |
15 |
p. 7429-7435 7 p. |
artikel |
34 |
Novel sterically hindered cannabinoid CB1 receptor ligands
|
Urbani, Paolo |
|
2008 |
16 |
15 |
p. 7510-7515 6 p. |
artikel |
35 |
Phenyl phosphotriester derivatives of AZT: Variations upon the SATE moiety
|
Villard, Anne-Laure |
|
2008 |
16 |
15 |
p. 7321-7329 9 p. |
artikel |
36 |
QSAR prediction of inhibition of aldose reductase for flavonoids
|
Mercader, Andrew G. |
|
2008 |
16 |
15 |
p. 7470-7476 7 p. |
artikel |
37 |
QSAR study of imidazoline antihypertensive drugs
|
Nikolic, Katarina |
|
2008 |
16 |
15 |
p. 7134-7140 7 p. |
artikel |
38 |
Remarkable DNA binding affinity and potential anticancer activity of pyrrolo[2,1-c][1,4]benzodiazepine–naphthalimide conjugates linked through piperazine side-armed alkane spacers
|
Kamal, Ahmed |
|
2008 |
16 |
15 |
p. 7218-7224 7 p. |
artikel |
39 |
Selective alkylation of βII-tubulin and thioredoxin-1 by structurally related subsets of aryl chloroethylureas leading to either anti-microtubules or redox modulating agents
|
Fortin, Jessica S. |
|
2008 |
16 |
15 |
p. 7277-7290 14 p. |
artikel |
40 |
Single-stranded DNA aptamers specific for antibiotics tetracyclines
|
Niazi, Javed H. |
|
2008 |
16 |
15 |
p. 7245-7253 9 p. |
artikel |
41 |
Structure–activity correlations for β-phenethylamines at human trace amine receptor 1
|
Lewin, Anita H. |
|
2008 |
16 |
15 |
p. 7415-7423 9 p. |
artikel |
42 |
Structure–activity relationship of flavonoids as influenza virus neuraminidase inhibitors and their in vitro anti-viral activities
|
Liu, Ai-Lin |
|
2008 |
16 |
15 |
p. 7141-7147 7 p. |
artikel |
43 |
Sulfur-substituted naphthalimides as photoactivatable anticancer agents: DNA interaction, fluorescence imaging, and phototoxic effects in cultured tumor cells
|
Ott, Ingo |
|
2008 |
16 |
15 |
p. 7107-7116 10 p. |
artikel |
44 |
Syntheses of phosphatidyl-β-d-glucoside analogues to probe antigen selectivity of monoclonal antibody ‘DIM21’
|
Greimel, Peter |
|
2008 |
16 |
15 |
p. 7210-7217 8 p. |
artikel |
45 |
Synthesis and antiviral evaluation of some new pyrazole and fused pyrazolopyrimidine derivatives
|
Rashad, Aymn E. |
|
2008 |
16 |
15 |
p. 7102-7106 5 p. |
artikel |
46 |
Synthesis and biological evaluation of new disubstituted analogues of 6-methoxy-3-(3′,4′,5′-trimethoxybenzoyl)-1H-indole (BPR0L075), as potential antivascular agents
|
Ty, Nancy |
|
2008 |
16 |
15 |
p. 7494-7503 10 p. |
artikel |
47 |
Synthesis and cytotoxic, anti-inflammatory, and anti-oxidant activities of 2′,5′-dialkoxylchalcones as cancer chemopreventive agents
|
Cheng, Jen-Hao |
|
2008 |
16 |
15 |
p. 7270-7276 7 p. |
artikel |
48 |
Synthesis and evaluation of pyrazolo[3,4-b]pyridines and its structural analogues as TNF-α and IL-6 inhibitors
|
Bharate, Sandip B. |
|
2008 |
16 |
15 |
p. 7167-7176 10 p. |
artikel |
49 |
Synthesis, DNA binding, and cytotoxic evaluation of new analogs of diallyldisulfide, an active principle of garlic
|
Rai, Santosh Kumar |
|
2008 |
16 |
15 |
p. 7302-7310 9 p. |
artikel |
50 |
Synthesis, inhibitory activities, and QSAR study of xanthone derivatives as α-glucosidase inhibitors
|
Liu, Yan |
|
2008 |
16 |
15 |
p. 7185-7192 8 p. |
artikel |
51 |
Synthesis of 3′-deoxy-3′-C-methyl nucleoside derivatives
|
Aljarah, Mohamed |
|
2008 |
16 |
15 |
p. 7436-7442 7 p. |
artikel |
52 |
Synthesis of scyllo-inositol derivatives and their effects on amyloid beta peptide aggregation
|
Sun, Yedi |
|
2008 |
16 |
15 |
p. 7177-7184 8 p. |
artikel |
53 |
The discovery of small molecule chemical probes of Bcl-XL and Mcl-1
|
Prakesch, Michael |
|
2008 |
16 |
15 |
p. 7443-7449 7 p. |
artikel |