nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Aplysia californica mediated cyclisation of novel 3′-modified NAD+ analogues: a role for hydrogen bonding in the recognition of cyclic adenosine 5′-diphosphate ribose
|
Mort, Christopher J.W |
|
2004 |
12 |
2 |
p. 475-487 13 p. |
artikel |
2 |
Combining NMR and molecular modelling in a drug delivery context: investigation of the multi-mode inclusion of a new NPY-5 antagonist bromobenzenesulfonamide into β-cyclodextrin
|
Uccello-Barretta, Gloria |
|
2004 |
12 |
2 |
p. 447-458 12 p. |
artikel |
3 |
Contributors to this issue
|
|
|
2004 |
12 |
2 |
p. I- 1 p. |
artikel |
4 |
Design, synthesis and structure–affinity relationships of aryloxyanilide derivatives as novel peripheral benzodiazepine receptor ligands
|
Okubo, Taketoshi |
|
2004 |
12 |
2 |
p. 423-438 16 p. |
artikel |
5 |
Dihydropyridine neuropeptide Y Y1 receptor antagonists 2
|
Poindexter, Graham S |
|
2004 |
12 |
2 |
p. 507-521 15 p. |
artikel |
6 |
Discovery, characterization and SAR of gambogic acid as a potent apoptosis inducer by a HTS assay
|
Zhang, Han-Zhong |
|
2004 |
12 |
2 |
p. 309-317 9 p. |
artikel |
7 |
Editorial Board
|
|
|
2004 |
12 |
2 |
p. IFC- 1 p. |
artikel |
8 |
Enzymatic synthesis of tea theaflavin derivatives and their anti-inflammatory and cytotoxic activities
|
Sang, Shengmin |
|
2004 |
12 |
2 |
p. 459-467 9 p. |
artikel |
9 |
Graphical contents list
|
|
|
2004 |
12 |
2 |
p. 301-306 6 p. |
artikel |
10 |
α-Hydroxyketones as inhibitors of urease
|
Tanaka, Toru |
|
2004 |
12 |
2 |
p. 501-505 5 p. |
artikel |
11 |
Instructions to Contributors
|
|
|
2004 |
12 |
2 |
p. III-VI nvt p. |
artikel |
12 |
Interaction of isofraxidin with human serum albumin
|
Liu, Jiaqin |
|
2004 |
12 |
2 |
p. 469-474 6 p. |
artikel |
13 |
Metabolism of 5′α,8′-cycloabscisic acid, a highly potent and long-lasting abscisic acid analogue, in radish seedlings
|
Todoroki, Yasushi |
|
2004 |
12 |
2 |
p. 363-370 8 p. |
artikel |
14 |
Muscarinic M2 antagonists: anthranilamide derivatives with exceptional selectivity and in vivo activity
|
Clader, John W |
|
2004 |
12 |
2 |
p. 319-326 8 p. |
artikel |
15 |
N-[4-(Methylsulfonylamino)benzyl]thiourea analogues as vanilloid receptor antagonists: analysis of structure–activity relationships for the ‘C-Region’
|
Lee, Jeewoo |
|
2004 |
12 |
2 |
p. 371-385 15 p. |
artikel |
16 |
Publisher's Announcement—new Regional Editor for Bioorganic & Medicinal Chemistry
|
|
|
2004 |
12 |
2 |
p. 307- 1 p. |
artikel |
17 |
Structure–activity relationships of globomycin analogues as antibiotics
|
Kiho, Toshihiro |
|
2004 |
12 |
2 |
p. 337-361 25 p. |
artikel |
18 |
Syntheses and receptor-binding studies of derivatives of the opioid antagonist naltrexone
|
Uwai, Koji |
|
2004 |
12 |
2 |
p. 417-421 5 p. |
artikel |
19 |
Synthesis and anti-inflammatory evaluation of 4-anilinofuro[2,3-b]quinoline and 4-phenoxyfuro[2,3-b]quinoline derivatives. Part 3
|
Chen, Yeh-Long |
|
2004 |
12 |
2 |
p. 387-392 6 p. |
artikel |
20 |
Synthesis, biological, and chiroptical activity of 3-phenyl-clavams
|
Cierpucha, Maciej |
|
2004 |
12 |
2 |
p. 405-416 12 p. |
artikel |
21 |
Synthesis, biological evaluation, and structural studies on N1 and C5 substituted cycloalkyl analogues of the pyrazole class of CB1 and CB2 ligands
|
Krishnamurthy, Mathangi |
|
2004 |
12 |
2 |
p. 393-404 12 p. |
artikel |
22 |
Thalidomide analogues demonstrate dual inhibition of both angiogenesis and prostate cancer
|
Capitosti, Scott M |
|
2004 |
12 |
2 |
p. 327-336 10 p. |
artikel |
23 |
The alkaloids and other constituents from the root and stem of Aristolochia elegans
|
Shi, Li-Shian |
|
2004 |
12 |
2 |
p. 439-446 8 p. |
artikel |
24 |
Three-dimensional quantitative structure–activity relationship analyses of piperidine-based CCR5 receptor antagonists
|
Song, Minghu |
|
2004 |
12 |
2 |
p. 489-499 11 p. |
artikel |