| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Activation of NFκB is inhibited by curcumin and related enones
|
Weber, Waylon M.
|
|
2006
|
14 |
7 |
p. 2450-2461
12 p.
|
artikel
|
| 2 |
2-Aminothiophene-3-carboxylates and carboxamides as adenosine A1 receptor allosteric enhancers
|
Nikolakopoulos, George
|
|
2006
|
14 |
7 |
p. 2358-2365
8 p.
|
artikel
|
| 3 |
Antimalarial activity: A QSAR modeling using CODESSA PRO software
|
Katritzky, Alan R.
|
|
2006
|
14 |
7 |
p. 2333-2357
25 p.
|
artikel
|
| 4 |
Apoptosis-inducing effect of epolactaene derivatives on BALL-1 cells
|
Kuramochi, Kouji
|
|
2006
|
14 |
7 |
p. 2151-2161
11 p.
|
artikel
|
| 5 |
Atom-based 3D-chiral quadratic indices. Part 2: Prediction of the corticosteroid-binding globulinbinding affinity of the 31 benchmark steroids data set
|
Castillo-Garit, Juan A.
|
|
2006
|
14 |
7 |
p. 2398-2408
11 p.
|
artikel
|
| 6 |
Bicyclic and tricyclic thiophenes as protein tyrosine phosphatase 1B inhibitors
|
Moretto, A.F.
|
|
2006
|
14 |
7 |
p. 2162-2177
16 p.
|
artikel
|
| 7 |
Carbonic anhydrase inhibitors: Transepithelial transport of thioureido sulfonamide inhibitors of the cancer-associated isozyme IX is dependent on efflux transporters
|
Vullo, Daniela
|
|
2006
|
14 |
7 |
p. 2418-2427
10 p.
|
artikel
|
| 8 |
Chemo-enzymatic synthesis of 1,4-oxazepanyl sugar as potent inhibitor of chitinase
|
Huang, Gang-Liang
|
|
2006
|
14 |
7 |
p. 2446-2449
4 p.
|
artikel
|
| 9 |
Chemotactic peptides: fMLF-OMe analogues incorporating proline–methionine chimeras as N-terminal residue
|
Mollica, Adriano
|
|
2006
|
14 |
7 |
p. 2253-2265
13 p.
|
artikel
|
| 10 |
Discovering novel chemical inhibitors of human cyclophilin A: Virtual screening, synthesis, and bioassay
|
Li, Jian
|
|
2006
|
14 |
7 |
p. 2209-2224
16 p.
|
artikel
|
| 11 |
Diversity-oriented chemical modification of heparin: Identification of charge-reduced N-acyl heparin derivatives having increased selectivity for heparin-binding proteins
|
Huang, Liusheng
|
|
2006
|
14 |
7 |
p. 2300-2313
14 p.
|
artikel
|
| 12 |
Editorial Board
|
|
|
2006
|
14 |
7 |
p. CO2-
1 p.
|
artikel
|
| 13 |
Effective discrimination of antimalarial potency of artemisinin compounds based on quantum chemical calculations of their reaction mechanism
|
Tonmunphean, Somsak
|
|
2006
|
14 |
7 |
p. 2082-2088
7 p.
|
artikel
|
| 14 |
Effect of cholesterol on DMPC phospholipid membranes and QSAR model construction in membrane-interaction QSAR study through molecular dynamics simulation
|
Liu, Jianzhong
|
|
2006
|
14 |
7 |
p. 2225-2234
10 p.
|
artikel
|
| 15 |
Efficient microwave enhanced regioselective synthesis of a series of benzimidazolyl/triazolyl spiro [indole-thiazolidinones] as potent antifungal agents and crystal structure of spiro[3 H -indole-3,2′-thiazolidine]-3′(1,2,4-triazol-3-yl)-2,4′(1 H )-dione
|
Dandia, Anshu
|
|
2006
|
14 |
7 |
p. 2409-2417
9 p.
|
artikel
|
| 16 |
Evaluation of fosmidomycin analogs as inhibitors of the Synechocystis sp. PCC6803 1-deoxy-d-xylulose 5-phosphate reductoisomerase
|
Woo, Youn-Hi
|
|
2006
|
14 |
7 |
p. 2375-2385
11 p.
|
artikel
|
| 17 |
Graphical contents list
|
|
|
2006
|
14 |
7 |
p. 2073-2081
9 p.
|
artikel
|
| 18 |
Instructions to contributors
|
|
|
2006
|
14 |
7 |
p. I-
1 p.
|
artikel
|
| 19 |
Macrocyclic inhibitors of the malarial aspartic proteases plasmepsin I, II, and IV
|
Ersmark, Karolina
|
|
2006
|
14 |
7 |
p. 2197-2208
12 p.
|
artikel
|
| 20 |
Novel α-aminophosphonic acids. Design, characterization, and biological activity
|
Naydenova, Emilia
|
|
2006
|
14 |
7 |
p. 2190-2196
7 p.
|
artikel
|
| 21 |
ORL1 and opioid receptor preferences of nociceptin and dynorphin A analogues with Dmp substituted for N-terminal aromatic residues
|
Sasaki, Yusuke
|
|
2006
|
14 |
7 |
p. 2433-2437
5 p.
|
artikel
|
| 22 |
Phosphoramidate and phosphate prodrugs of (−)-β-d-(2R,4R)-dioxolane-thymine: Synthesis, anti-HIV activity and stability studies
|
Liang, Yuzeng
|
|
2006
|
14 |
7 |
p. 2178-2189
12 p.
|
artikel
|
| 23 |
Safrole oxide induces apoptosis by up-regulating Fas and FasL instead of integrin β4 in A549 human lung cancer cells
|
Du, AiYing
|
|
2006
|
14 |
7 |
p. 2438-2445
8 p.
|
artikel
|
| 24 |
Self-aggregation of synthetic zinc chlorophyll derivative possessing a perfluoroalkyl group in a fluorinated solvent
|
Shibata, Reiko
|
|
2006
|
14 |
7 |
p. 2235-2241
7 p.
|
artikel
|
| 25 |
Spectroscopic studies of the interaction between hypocrellin B and human serum albumin
|
Zhao, Baozhong
|
|
2006
|
14 |
7 |
p. 2428-2432
5 p.
|
artikel
|
| 26 |
Syntheses and evaluation of fluorinated conformationally restricted analogues of GABA as potential inhibitors of GABA aminotransferase
|
Wang, Zhiyong
|
|
2006
|
14 |
7 |
p. 2242-2252
11 p.
|
artikel
|
| 27 |
Synthesis and anti-HIV activity of bi-functional betulinic acid derivatives
|
Huang, Li
|
|
2006
|
14 |
7 |
p. 2279-2289
11 p.
|
artikel
|
| 28 |
Synthesis and anti-HIV activity of new alkenyldiarylmethane (ADAM) non-nucleoside reverse transcriptase inhibitors (NNRTIs) incorporating benzoxazolone and benzisoxazole rings
|
Deng, Bo-Liang
|
|
2006
|
14 |
7 |
p. 2366-2374
9 p.
|
artikel
|
| 29 |
Synthesis and biological evaluation of B-ring analogues of (−)-rhazinilam
|
Décor, Anne
|
|
2006
|
14 |
7 |
p. 2314-2332
19 p.
|
artikel
|
| 30 |
Synthesis and biological evaluation of conformationally constrained analogs of the antitumor agents XK469 and SH80. Part 5
|
Hazeldine, Stuart T.
|
|
2006
|
14 |
7 |
p. 2462-2467
6 p.
|
artikel
|
| 31 |
Synthesis and pharmacology of 11-nor-1-methoxy-9-hydroxyhexahydrocannabinols and 11-nor-1-deoxy-9-hydroxyhexahydrocannabinols: New selective ligands for the cannabinoid CB2 receptor
|
Marriott, Karla-Sue C.
|
|
2006
|
14 |
7 |
p. 2386-2397
12 p.
|
artikel
|
| 32 |
Synthesis of new bioactive venlafaxine analogs: Novel thiazolidin-4-ones as antimicrobials
|
Kavitha, C.V.
|
|
2006
|
14 |
7 |
p. 2290-2299
10 p.
|
artikel
|
| 33 |
Time-dependent inhibitors of trypanothione reductase: Analogues of the spermidine alkaloid lunarine and related natural products
|
Hamilton, Chris J.
|
|
2006
|
14 |
7 |
p. 2266-2278
13 p.
|
artikel
|
| 34 |
Tricyclic pharmacophore-based molecules as novel integrin αvβ3 antagonists. Part 1: Design and synthesis of a lead compound exhibiting αvβ3/αIIbβ3 dual antagonistic activity
|
Kubota, Dai
|
|
2006
|
14 |
7 |
p. 2089-2108
20 p.
|
artikel
|
| 35 |
Tricyclic pharmacophore-based molecules as novel integrin αvβ3 antagonists. Part III: Synthesis of potent antagonists with αvβ3/αIIbβ3 dual activity and improved water solubility
|
Ishikawa, Minoru
|
|
2006
|
14 |
7 |
p. 2131-2150
20 p.
|
artikel
|
| 36 |
Tricyclic pharmacophore-based molecules as novel integrin αvβ3 antagonists. Part 2: Synthesis of potent αvβ3/αIIbβ3 dual antagonists
|
Ishikawa, Minoru
|
|
2006
|
14 |
7 |
p. 2109-2130
22 p.
|
artikel
|
Tijdschrift beschrijving