| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Antimycobacterial compounds. New pyrrole derivatives of BM212
|
Biava, Mariangela
|
|
2004
|
12 |
6 |
p. 1453-1458
6 p.
|
artikel
|
| 2 |
Bioorganic & Medicinal Chemistry Symposia-in-Print
|
|
|
2004
|
12 |
6 |
p. 1275-
1 p.
|
artikel
|
| 3 |
Contributors to this issue
|
|
|
2004
|
12 |
6 |
p. I-
1 p.
|
artikel
|
| 4 |
Corrigendum to “Structure–activity relationships of antileishmanial and antimalarial chalcones” (Bioorg. Chem. 2003, 11, 2729–2738]
|
Liu, Mei
|
|
2004
|
12 |
6 |
p. 1569-
1 p.
|
artikel
|
| 5 |
Deoxynucleic guanidine
|
Challa, Hemavathi
|
|
2004
|
12 |
6 |
p. 1475-1481
7 p.
|
artikel
|
| 6 |
Design of N-acetyl-6-sulfo-β-d-glucosaminide-based inhibitors of influenza virus sialidase
|
Sasaki, Kenji
|
|
2004
|
12 |
6 |
p. 1367-1375
9 p.
|
artikel
|
| 7 |
Design, synthesis, and α1-adrenoceptor binding properties of new arylpiperazine derivatives bearing a flavone nucleus as the terminal heterocyclic molecular portion
|
Betti, Laura
|
|
2004
|
12 |
6 |
p. 1527-1535
9 p.
|
artikel
|
| 8 |
Design, synthesis, and characterization of peptide nanostructures having ion channel activity
|
Biron, Eric
|
|
2004
|
12 |
6 |
p. 1279-1290
12 p.
|
artikel
|
| 9 |
8,9-Dihydroxy-1,2,3,11b-tetrahydrochromeno[4,3,2,-de]isoquinoline (dinoxyline), a high affinity and potent agonist at all dopamine receptor isoforms
|
Grubbs, Russell A
|
|
2004
|
12 |
6 |
p. 1403-1412
10 p.
|
artikel
|
| 10 |
1,4-Dihydroxyxanthone modulates the adhesive property of endothelial cells by inhibiting intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1) and E-selectin
|
Madan, Babita
|
|
2004
|
12 |
6 |
p. 1431-1437
7 p.
|
artikel
|
| 11 |
2,3-Disubstituted 6-azabicyclo[3.2.1]octanes as novel dopamine transporter inhibitors
|
Quirante, Josefina
|
|
2004
|
12 |
6 |
p. 1383-1391
9 p.
|
artikel
|
| 12 |
Editorial board
|
|
|
2004
|
12 |
6 |
p. IFC-
1 p.
|
artikel
|
| 13 |
Electrochemical release from gold–thiolate electrodes for controlled insertion of ion channels into bilayer membranes
|
Buchmann, M.B
|
|
2004
|
12 |
6 |
p. 1315-1324
10 p.
|
artikel
|
| 14 |
Engineering charge selectivity in model ion channels
|
Lougheed, Tyler
|
|
2004
|
12 |
6 |
p. 1337-1342
6 p.
|
artikel
|
| 15 |
Equol, a natural estrogenic metabolite from soy isoflavones
|
Muthyala, Rajeev S
|
|
2004
|
12 |
6 |
p. 1559-1567
9 p.
|
artikel
|
| 16 |
Functional, synthetic organic chemical models of cellular ion channels
|
Gokel, George W
|
|
2004
|
12 |
6 |
p. 1291-1304
14 p.
|
artikel
|
| 17 |
Further insights on the structural aspects of PLA2 inhibition by γ-hydroxybutenolide-containing natural products: a comparative study on petrosaspongiolides M–R
|
Monti, Maria Chiara
|
|
2004
|
12 |
6 |
p. 1467-1474
8 p.
|
artikel
|
| 18 |
Gramicidin-based channel systems for the detection of protein–ligand interaction
|
Futaki, Shiroh
|
|
2004
|
12 |
6 |
p. 1343-1350
8 p.
|
artikel
|
| 19 |
Graphical contents list
|
|
|
2004
|
12 |
6 |
p. 1265-1273
9 p.
|
artikel
|
| 20 |
Instructions to contributors
|
|
|
2004
|
12 |
6 |
p. III-VI
nvt p.
|
artikel
|
| 21 |
Kinetic and structural consequences of the leaving group in substrates of a class C β-lactamase
|
Ahn, Yong-Mo
|
|
2004
|
12 |
6 |
p. 1537-1542
6 p.
|
artikel
|
| 22 |
5-N-Substituted-2-(substituted benzenesulphonyl) glutamines as antitumor agents. Part II: Synthesis, biological activity and QSAR study
|
Samanta, Soma
|
|
2004
|
12 |
6 |
p. 1413-1423
11 p.
|
artikel
|
| 23 |
Outer surface modification of synthetic multifunctional pores
|
Talukdar, Pinaki
|
|
2004
|
12 |
6 |
p. 1325-1336
12 p.
|
artikel
|
| 24 |
QSAR study on some anti-HIV HEPT analogues using physicochemical and topological parameters
|
Gayen, Shovanlal
|
|
2004
|
12 |
6 |
p. 1493-1503
11 p.
|
artikel
|
| 25 |
QSPR/QSAR in N-[(dimethylamine)methyl] benzamides substituents groups influence upon electronic distribution and local anesthetics activity
|
Tavares, Leoberto Costa
|
|
2004
|
12 |
6 |
p. 1377-1381
5 p.
|
artikel
|
| 26 |
Synthesis and biological evaluation of 2-(4-fluorophenoxy)-2-phenyl-ethyl piperazines as serotonin-selective reuptake inhibitors with a potentially improved adverse reaction profile
|
Dorsey, James M
|
|
2004
|
12 |
6 |
p. 1483-1491
9 p.
|
artikel
|
| 27 |
Synthesis and biological evaluation of 6-substituted purine and 9-β-d-ribofuranosyl purine analogues
|
Wang, Jun-Feng
|
|
2004
|
12 |
6 |
p. 1425-1429
5 p.
|
artikel
|
| 28 |
Synthesis and duplex DNA recognition studies of oligonucleotides containing a ureido isoindolin-1-one homo-N-nucleoside. A comparison of host–guest and DNA recognition studies
|
Mertz, Eric
|
|
2004
|
12 |
6 |
p. 1517-1526
10 p.
|
artikel
|
| 29 |
Synthesis and in vitro evaluation of S-acyl-3-thiopropyl prodrugs of Foscarnet
|
Gagnard, Valérie
|
|
2004
|
12 |
6 |
p. 1393-1402
10 p.
|
artikel
|
| 30 |
Synthesis and SAR of tetracyclic pyrroloquinolones as phosphodiesterase 5 inhibitors
|
Jiang, Weiqin
|
|
2004
|
12 |
6 |
p. 1505-1515
11 p.
|
artikel
|
| 31 |
Synthesis and selective cyclooxygenase-2 (COX-2) inhibitory activity of a series of novel bicyclic pyrazoles
|
Ranatunge, Ramani R.
|
|
2004
|
12 |
6 |
p. 1357-1366
10 p.
|
artikel
|
| 32 |
Synthesis and structure–activity relationships of a new model of arylpiperazines. Part 7: Study of the influence of lipophilic factors at the terminal amide fragment on 5-HT1A affinity/selectivity
|
López-Rodrı́guez, Marı́a L
|
|
2004
|
12 |
6 |
p. 1551-1557
7 p.
|
artikel
|
| 33 |
Synthesis and structure/NMDA receptor affinity relationships of 1-substituted tetrahydro-3-benzazepines
|
Krull, Olaf
|
|
2004
|
12 |
6 |
p. 1439-1451
13 p.
|
artikel
|
| 34 |
Synthesis of bicyclic biaryls as glucose-6-phosphatase inhibitors
|
Farhanullah,
|
|
2004
|
12 |
6 |
p. 1543-1549
7 p.
|
artikel
|
| 35 |
Synthesis of novel 4- and 5-substituted benzyl ether derivatives of vesamicol and in vitro evaluation of their binding properties to the vesicular acetylcholine transporter site
|
Scheunemann, Matthias
|
|
2004
|
12 |
6 |
p. 1459-1465
7 p.
|
artikel
|
| 36 |
Synthetic ion channels
|
Koert, Ulrich
|
|
2004
|
12 |
6 |
p. 1277-
1 p.
|
artikel
|
| 37 |
Toward an HDAC6 inhibitor: synthesis and conformational analysis of cyclic hexapeptide hydroxamic acid designed from α-tubulin sequence
|
Jose, Binoy
|
|
2004
|
12 |
6 |
p. 1351-1356
6 p.
|
artikel
|
| 38 |
Water molecules in hydroxy/acid networks as a competition between dynamics and bonding. Synthesis of a wet hydrophobic pore
|
Pérez-Hernández, Natalia
|
|
2004
|
12 |
6 |
p. 1305-1314
10 p.
|
artikel
|
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