| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acidic heterocycles as novel hydrophilic pharmacophore of androgen receptor ligands with a carborane core structure
|
Fujii, Shinya
|
|
2009
|
17 |
1 |
p. 344-350
7 p.
|
artikel
|
| 2 |
Alantrypinone and its derivatives: Synthesis and antagonist activity toward insect GABA receptors
|
Watanabe, Takayuki
|
|
2009
|
17 |
1 |
p. 94-110
17 p.
|
artikel
|
| 3 |
Antibacterial 5′-O-(N-dipeptidyl)-sulfamoyladenosines
|
Van de Vijver, P.
|
|
2009
|
17 |
1 |
p. 260-269
10 p.
|
artikel
|
| 4 |
Arthrobacter sp. lipase immobilization for preparation of enantiopure masked β-amino alcohols
|
Chaubey, Asha
|
|
2009
|
17 |
1 |
p. 29-34
6 p.
|
artikel
|
| 5 |
A simple synthesis of four stereoisomers of roseoside and their inhibitory activity on leukotriene release from mice bone marrow-derived cultured mast cells
|
Yajima, Arata
|
|
2009
|
17 |
1 |
p. 189-194
6 p.
|
artikel
|
| 6 |
6-Bicycloaryl substituted (S)- and (R)-5,6-dihydro-2H-pyran-2-ones: Asymmetric synthesis, and anti-proliferative properties
|
Kasaplar, Pınar
|
|
2009
|
17 |
1 |
p. 311-318
8 p.
|
artikel
|
| 7 |
Comparison of benzil and trifluoromethyl ketone (TFK)-mediated carboxylesterase inhibition using classical and 3D-quantitative structure–activity relationship analysis
|
Harada, Toshiyuki
|
|
2009
|
17 |
1 |
p. 149-164
16 p.
|
artikel
|
| 8 |
Corrigendum to “Alachalasins A–G, new cytochalasins from the fungus Stachybotrys charatum” [Bioorg. Med. Chem. 16 (2008) 2627–2634]
|
Zhang, Yonggang
|
|
2009
|
17 |
1 |
p. 428-
1 p.
|
artikel
|
| 9 |
Corrigendum to “Fluorinated methylenecyclopropane analogues of nucleosides. Synthesis and antiviral activity of (Z)- and (E)-9-{[(2-fluoromethyl-2-hydroxymethyl)-cyclopropylidene]methyl}adenine and -guanine” [Bioorg. Med. Chem. 16 (2008) 2148–2155]
|
Li, Chengwei
|
|
2009
|
17 |
1 |
p. 427-
1 p.
|
artikel
|
| 10 |
Design, synthesis and biological evaluation of novel bicyclo[1.1.1]pentane-based ω-acidic amino acids as glutamate receptors ligands
|
Filosa, Rosanna
|
|
2009
|
17 |
1 |
p. 242-250
9 p.
|
artikel
|
| 11 |
Design, Synthesis and Pharmacological Screening of Novel Antihypertensive Agents Using Hybrid Approach
|
Bhandari, Shashikant V.
|
|
2009
|
17 |
1 |
p. 390-400
11 p.
|
artikel
|
| 12 |
Discovery and structure–activity relationships of 4-aminoquinazoline derivatives, a novel class of opioid receptor like-1 (ORL1) antagonists
|
Okano, Masahiko
|
|
2009
|
17 |
1 |
p. 119-132
14 p.
|
artikel
|
| 13 |
Discovery of novel analgesic and anti-inflammatory 3-arylamine-imidazo[1,2-a]pyridine symbiotic prototypes
|
Lacerda, Renata B.
|
|
2009
|
17 |
1 |
p. 74-84
11 p.
|
artikel
|
| 14 |
Editorial board
|
|
|
2009
|
17 |
1 |
p. IFC-
1 p.
|
artikel
|
| 15 |
Effect of methyl substitution in a ligand on the selectivity and binding affinity for a nucleobase: A case study with isoxanthopterin and its derivatives
|
Rajendar, Burki
|
|
2009
|
17 |
1 |
p. 351-359
9 p.
|
artikel
|
| 16 |
Enaminones 8: CoMFA and CoMSIA studies on some anticonvulsant enaminones
|
Jackson, Patrice L.
|
|
2009
|
17 |
1 |
p. 133-140
8 p.
|
artikel
|
| 17 |
Facilitated phospholipid translocation in vesicles and nucleated cells using synthetic small molecule scramblases
|
DiVittorio, Kristy M.
|
|
2009
|
17 |
1 |
p. 141-148
8 p.
|
artikel
|
| 18 |
4-Fluoro-N-butylphenylacetamide (H6) inhibits cell growth via cell-cycle arrest and apoptosis in human cervical cancer cells
|
Liu, Chung-Hsien
|
|
2009
|
17 |
1 |
p. 42-48
7 p.
|
artikel
|
| 19 |
Graphical contents list
|
|
|
2009
|
17 |
1 |
p. 1-12
12 p.
|
artikel
|
| 20 |
High transfection efficiency and low toxicity cationic lipids with aminoglycerol–diamine conjugate
|
Yingyongnarongkul, Boon-ek
|
|
2009
|
17 |
1 |
p. 176-188
13 p.
|
artikel
|
| 21 |
Identification and physiological evaluation of the components from Citrus fruits as potential drugs for anti-corpulence and anticancer
|
Hirata, Toshifumi
|
|
2009
|
17 |
1 |
p. 25-28
4 p.
|
artikel
|
| 22 |
Identification of Aquaporin 4 inhibitors using in vitro and in silico methods
|
Huber, Vincent J.
|
|
2009
|
17 |
1 |
p. 411-417
7 p.
|
artikel
|
| 23 |
Identification of trimannoside-recognizing peptide sequences from a T7 phage display screen using a QCM device
|
Nishiyama, Kazusa
|
|
2009
|
17 |
1 |
p. 195-202
8 p.
|
artikel
|
| 24 |
Inhibition of Aquaporin 4 by antiepileptic drugs
|
Huber, Vincent J.
|
|
2009
|
17 |
1 |
p. 418-424
7 p.
|
artikel
|
| 25 |
Instructions to contributors
|
|
|
2009
|
17 |
1 |
p. I-
1 p.
|
artikel
|
| 26 |
Molecular design of protein-based nanocapsules for stimulus-responsive characteristics
|
Sao, Kentaro
|
|
2009
|
17 |
1 |
p. 85-93
9 p.
|
artikel
|
| 27 |
Molecular modelling studies, synthesis and biological activity of a series of novel bisnaphthalimides and their development as new DNA topoisomerase II inhibitors
|
Filosa, Rosanna
|
|
2009
|
17 |
1 |
p. 13-24
12 p.
|
artikel
|
| 28 |
Novel chemotactic For-Met-Leu-Phe-OMe (fMLF-OMe) analogues based on Met residue replacement by 4-amino-proline scaffold: Synthesis and bioactivity
|
Torino, Domenica
|
|
2009
|
17 |
1 |
p. 251-259
9 p.
|
artikel
|
| 29 |
Novel potent and highly selective human A3 adenosine receptor antagonists belonging to the 4-amido-2-arylpyrazolo[3,4-c]quinoline series: Molecular docking analysis and pharmacological studies
|
Colotta, Vittoria
|
|
2009
|
17 |
1 |
p. 401-410
10 p.
|
artikel
|
| 30 |
Potent and orally bioavailable CCR4 antagonists: Synthesis and structure–activity relationship study of 2-aminoquinazolines
|
Yokoyama, Kazuhiro
|
|
2009
|
17 |
1 |
p. 64-73
10 p.
|
artikel
|
| 31 |
QSAR and complex network study of the chiral HMGR inhibitor structural diversity
|
García, Isela
|
|
2009
|
17 |
1 |
p. 165-175
11 p.
|
artikel
|
| 32 |
QSAR studies on BK channel activators
|
Coi, Alessio
|
|
2009
|
17 |
1 |
p. 319-325
7 p.
|
artikel
|
| 33 |
Radiosynthesis, in vitro and in vivo evaluation of 123I-labeled anandamide analogues for mapping brain FAAH
|
wyffels, Leonie
|
|
2009
|
17 |
1 |
p. 49-56
8 p.
|
artikel
|
| 34 |
Search for new pharmacophores for antimalarial activity. Part II: Synthesis and antimalarial activity of new 6-ureido-4-anilinoquinazolines
|
Madapa, S.
|
|
2009
|
17 |
1 |
p. 222-234
13 p.
|
artikel
|
| 35 |
Search for new pharmacophores for antimalarial activity. Part I: Synthesis and antimalarial activity of new 2-methyl-6-ureido-4-quinolinamides
|
Madapa, S.
|
|
2009
|
17 |
1 |
p. 203-221
19 p.
|
artikel
|
| 36 |
Selective activity against Mycobacterium tuberculosis of new quinoxaline 1,4-di-N-oxides
|
Vicente, Esther
|
|
2009
|
17 |
1 |
p. 385-389
5 p.
|
artikel
|
| 37 |
Spiro(imidazo[1,2-a]pyrano[2,3-c]pyridine-9-indenes) as inhibitors of gastric acid secretion
|
Palmer, Andreas Marc
|
|
2009
|
17 |
1 |
p. 368-384
17 p.
|
artikel
|
| 38 |
Stereoselective inhibition of serotonin re-uptake and phosphodiesterase by dual inhibitors as potential agents for depression
|
Cashman, John R.
|
|
2009
|
17 |
1 |
p. 337-343
7 p.
|
artikel
|
| 39 |
Structure–activity relationship studies of 5-benzylaminoimidazo[1,2-c]pyrimidine-8-carboxamide derivatives as potent, highly selective ZAP-70 kinase inhibitors
|
Hirabayashi, Akihito
|
|
2009
|
17 |
1 |
p. 284-294
11 p.
|
artikel
|
| 40 |
Support for small molecule inhibition of aquaporin 4
|
Huber, Vincent J.
|
|
2009
|
17 |
1 |
p. 425-426
2 p.
|
artikel
|
| 41 |
Syntheses and biological activities of fluorescent-labeled analogs of acylpolyamine toxin NPTX-594 isolated from the venom of Madagascar Joro spider
|
Nishimaru, Takahiro
|
|
2009
|
17 |
1 |
p. 57-63
7 p.
|
artikel
|
| 42 |
Synthesis and antimalarial activity of new 4-amino-7-chloroquinolyl amides, sulfonamides, ureas and thioureas
|
Ekoue-Kovi, Kekeli
|
|
2009
|
17 |
1 |
p. 270-283
14 p.
|
artikel
|
| 43 |
Synthesis and biological activity of 1,4-dihydrobenzothiopyrano[4,3-c]pyrazole derivatives, novel pro-apoptotic mitochondrial targeted agents
|
Dalla Via, L.
|
|
2009
|
17 |
1 |
p. 326-336
11 p.
|
artikel
|
| 44 |
Synthesis and biological properties of Pachastrissamine (jaspine B) and diastereoisomeric jaspines
|
Canals, Daniel
|
|
2009
|
17 |
1 |
p. 235-241
7 p.
|
artikel
|
| 45 |
Synthesis and evaluation of electron-rich curcumin analogues
|
Amolins, Michael W.
|
|
2009
|
17 |
1 |
p. 360-367
8 p.
|
artikel
|
| 46 |
Synthesis and in vitro activities of a new antiviral duplex drug linking Zidovudine (AZT) and Foscarnet (PFA) via an octadecylglycerol residue
|
Schott, Herbert
|
|
2009
|
17 |
1 |
p. 303-310
8 p.
|
artikel
|
| 47 |
Synthesis and SAR of 6-chloro-4-fluoroalkylamino-2-heteroaryl-5-(substituted)phenylpyrimidines as anti-cancer agents
|
Zhang, Nan
|
|
2009
|
17 |
1 |
p. 111-118
8 p.
|
artikel
|
| 48 |
Synthesis, antichagasic in vitro evaluation, cytotoxicity assays, molecular modeling and SAR/QSAR studies of a 2-phenyl-3-(1-phenyl-1H-pyrazol-4-yl)-acrylic acid benzylidene-carbohydrazide series
|
Vera-DiVaio, Maria A.F.
|
|
2009
|
17 |
1 |
p. 295-302
8 p.
|
artikel
|
| 49 |
Tyrosinase inhibitory effects of 1,3-diphenylpropanes from Broussonetia kazinoki
|
Baek, Yoon Su
|
|
2009
|
17 |
1 |
p. 35-41
7 p.
|
artikel
|
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