| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A combined approach of docking and 3D QSAR study of β-ketoacyl-acyl carrier protein synthase III (FabH) inhibitors
|
Ashek, Ali
|
|
2006
|
14 |
5 |
p. 1474-1482
9 p.
|
artikel
|
| 2 |
Activity of lupane triterpenoids from Maytenus species as inhibitors of nitric oxide and prostaglandin E2
|
Reyes, Carolina P.
|
|
2006
|
14 |
5 |
p. 1573-1579
7 p.
|
artikel
|
| 3 |
Advances in the synthesis and recent therapeutic applications of 1,2,4-thiadiazole heterocycles
|
Castro, Ana
|
|
2006
|
14 |
5 |
p. 1644-1652
9 p.
|
artikel
|
| 4 |
Affinity prediction on A1 adenosine receptor agonists: The chemometric approach
|
Fossa, Paola
|
|
2006
|
14 |
5 |
p. 1348-1363
16 p.
|
artikel
|
| 5 |
Classification of dopamine antagonists using functional feature hypothesis and topological descriptors
|
Kim, Hye-Jung
|
|
2006
|
14 |
5 |
p. 1454-1461
8 p.
|
artikel
|
| 6 |
Corrigendum to “Molecular modeling and 3D-QSAR studies of indolomorphinan derivatives as kappa opioid antagonists” [Bioorg. Med. Chem. 14 (2006) 601–610]
|
Li, Wei
|
|
2006
|
14 |
5 |
p. 1671-
1 p.
|
artikel
|
| 7 |
Design, synthesis, and biological activity of novel factor Xa inhibitors: Improving metabolic stability by S1 and S4 ligand modification
|
Komoriya, Satoshi
|
|
2006
|
14 |
5 |
p. 1309-1330
22 p.
|
artikel
|
| 8 |
Design, synthesis, and evaluation of novel galloyl pyrrolidine derivatives as potential anti-tumor agents
|
Li, Xun
|
|
2006
|
14 |
5 |
p. 1287-1293
7 p.
|
artikel
|
| 9 |
DFT study of the reductive decomposition of artemisinin
|
Taranto, Alex Gutterres
|
|
2006
|
14 |
5 |
p. 1546-1557
12 p.
|
artikel
|
| 10 |
Direct observation (NMR) of the efficacy of glucagon receptor antagonists in murine liver expressing the human glucagon receptor
|
Cohen, Sheila M.
|
|
2006
|
14 |
5 |
p. 1506-1517
12 p.
|
artikel
|
| 11 |
Discovery of potent and selective PARP-1 and PARP-2 inhibitors: SBDD analysis via a combination of X-ray structural study and homology modeling
|
Ishida, Junya
|
|
2006
|
14 |
5 |
p. 1378-1390
13 p.
|
artikel
|
| 12 |
3D-QSAR studies on tripeptide aldehyde inhibitors of proteasome using CoMFA and CoMSIA methods
|
Zhu, Yong-Qiang
|
|
2006
|
14 |
5 |
p. 1483-1496
14 p.
|
artikel
|
| 13 |
3D QSAR study of hypolipidemic asarones by comparative molecular surface analysis
|
Magdziarz, Tomasz
|
|
2006
|
14 |
5 |
p. 1630-1643
14 p.
|
artikel
|
| 14 |
Editorial Board
|
|
|
2006
|
14 |
5 |
p. CO2-
1 p.
|
artikel
|
| 15 |
Evaluation of aldose reductase inhibition and docking studies of some secondary metabolites, isolated from Origanum vulgare L. ssp. hirtum
|
Koukoulitsa, Catherine
|
|
2006
|
14 |
5 |
p. 1653-1659
7 p.
|
artikel
|
| 16 |
Graphical contents list
|
|
|
2006
|
14 |
5 |
p. 1277-1286
10 p.
|
artikel
|
| 17 |
Human serum albumin interaction with formononetin studied using fluorescence anisotropy, FT-IR spectroscopy, and molecular modeling methods
|
Li, Ying
|
|
2006
|
14 |
5 |
p. 1431-1436
6 p.
|
artikel
|
| 18 |
Inactivation of bovine plasma amine oxidase by haloallylamines
|
Kim, Jisook
|
|
2006
|
14 |
5 |
p. 1444-1453
10 p.
|
artikel
|
| 19 |
Instructions to contributors
|
|
|
2006
|
14 |
5 |
p. I-
1 p.
|
artikel
|
| 20 |
In vitro oxidative metabolism study of (−)-rhazinilam
|
Décor, Anne
|
|
2006
|
14 |
5 |
p. 1558-1564
7 p.
|
artikel
|
| 21 |
Microwave enhanced solid support synthesis of fluorine containing benzopyrano-triazolo-thiadiazepines as potent anti-fungal agents
|
Dandia, Anshu
|
|
2006
|
14 |
5 |
p. 1303-1308
6 p.
|
artikel
|
| 22 |
Modelling, synthesis and biological evaluation of novel glucuronide-based probes of Vibrio cholerae sialidase
|
Mann, Maretta C.
|
|
2006
|
14 |
5 |
p. 1518-1537
20 p.
|
artikel
|
| 23 |
New substrates and inhibitors of γ-aminobutyric acid aminotransferase containing bioisosteres of the carboxylic acid group: Design, synthesis, and biological activity
|
Yuan, Hai
|
|
2006
|
14 |
5 |
p. 1331-1338
8 p.
|
artikel
|
| 24 |
Polyamine conjugates of meso-tritolylporphyrin and protoporphyrin IX: Potential agents for photodynamic therapy of cancers
|
Sol, Vincent
|
|
2006
|
14 |
5 |
p. 1364-1377
14 p.
|
artikel
|
| 25 |
Solid phase synthesis and antiprotozoal evaluation of di- and trisubstituted 5′-carboxamidoadenosine analogues
|
Rodenko, Boris
|
|
2006
|
14 |
5 |
p. 1618-1629
12 p.
|
artikel
|
| 26 |
Stereoselective synthesis and anti-inflammatory activities of 6- and 7-membered dioxacycloalkanes
|
Gu, Keli
|
|
2006
|
14 |
5 |
p. 1339-1347
9 p.
|
artikel
|
| 27 |
Structural basis for DNA-cleaving activity of resveratrol in the presence of Cu(II)
|
Fukuhara, Kiyoshi
|
|
2006
|
14 |
5 |
p. 1437-1443
7 p.
|
artikel
|
| 28 |
Structure–activity relationships of a series of tariquidar analogs as multidrug resistance modulators
|
Globisch, Christoph
|
|
2006
|
14 |
5 |
p. 1588-1598
11 p.
|
artikel
|
| 29 |
Structure–intrinsic activity relationship studies in the group of 1-imido/amido substituted 4-(4-arylpiperazin-1-yl)cyclohexane derivatives; new, potent 5-HT1A receptor agents with anxiolytic- like activity
|
Bojarski, Andrzej J.
|
|
2006
|
14 |
5 |
p. 1391-1402
12 p.
|
artikel
|
| 30 |
Studies of interaction of trichloro{η2-cis-N,N-dimethyl-1-[6-(N′,N′-dimethyl-ammoniummethyl)-cyclohex-3-ene-1-yl]-methylammonium}platinum(II) chloride with DNA: Effects on secondary and tertiary structures of DNA. Cytotoxic assays on human ovarian cancer cell lines, resistant and non-resistant to cisplatin
|
Gay, Marina
|
|
2006
|
14 |
5 |
p. 1565-1572
8 p.
|
artikel
|
| 31 |
Substituted phenanthrenes with basic amino side chains: A new series of anti-breast cancer agents
|
Shagufta,
|
|
2006
|
14 |
5 |
p. 1497-1505
9 p.
|
artikel
|
| 32 |
Synthesis and biological evaluation of a series of flavone derivatives as potential radioligands for imaging the multidrug resistance-associated protein 1 (ABCC1/MRP1)
|
Mavel, Sylvie
|
|
2006
|
14 |
5 |
p. 1599-1607
9 p.
|
artikel
|
| 33 |
Synthesis and biological evaluation of 9-(5′,5′-difluoro-5′-phosphonopentyl)guanine derivatives for PNP-inhibitors
|
Hikishima, Sadao
|
|
2006
|
14 |
5 |
p. 1660-1670
11 p.
|
artikel
|
| 34 |
Synthesis and biological evaluation of new non-imidazole H3-receptor antagonists of the 2-aminobenzimidazole series
|
Rivara, Mirko
|
|
2006
|
14 |
5 |
p. 1413-1424
12 p.
|
artikel
|
| 35 |
Synthesis and in vitro activities of ferrocenic aminohydroxynaphthoquinones against Toxoplasma gondii and Plasmodium falciparum
|
Baramee, Apiwat
|
|
2006
|
14 |
5 |
p. 1294-1302
9 p.
|
artikel
|
| 36 |
Synthesis of chalcone analogues with increased antileishmanial activity
|
Boeck, Paula
|
|
2006
|
14 |
5 |
p. 1538-1545
8 p.
|
artikel
|
| 37 |
Synthesis of hypermodified adenosine derivatives as selective adenosine A3 receptor ligands
|
Cosyn, Liesbet
|
|
2006
|
14 |
5 |
p. 1403-1412
10 p.
|
artikel
|
| 38 |
The development of 3D-QSAR study and recursive partitioning of heterocyclic quinone derivatives with antifungal activity
|
Choi, Su-Young
|
|
2006
|
14 |
5 |
p. 1608-1617
10 p.
|
artikel
|
| 39 |
The 3D-QSAR analysis of 4(3H)-quinazolinone derivatives with dithiocarbamate side chains on thymidylate synthase
|
Liu, Shiying
|
|
2006
|
14 |
5 |
p. 1425-1430
6 p.
|
artikel
|
| 40 |
Theoretical proton affinities of α1 adrenoceptor ligands
|
Kinsella, Gemma K.
|
|
2006
|
14 |
5 |
p. 1580-1587
8 p.
|
artikel
|
| 41 |
Understanding the structure–activity and structure–selectivity correlation of cyclic guanine derivatives as phosphodiesterase-5 inhibitors by molecular docking, CoMFA and CoMSIA analyses
|
Yang, Guang-Fu
|
|
2006
|
14 |
5 |
p. 1462-1473
12 p.
|
artikel
|
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