nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Acetyltransfer in natural product biosynthesis––functional cloning and molecular analysis of vinorine synthase
|
Bayer, Anja |
|
2004 |
12 |
10 |
p. 2787-2795 9 p. |
artikel |
2 |
Aminyl and iminyl radicals from arylhydrazones in the photo-induced DNA cleavage
|
Ru Hwu, Jih |
|
2004 |
12 |
10 |
p. 2509-2515 7 p. |
artikel |
3 |
An investigation of the N-demethylation of 3-deoxymorphine and the affinity of the alkylation products to μ, δ, and κ receptors
|
Csutoras, Csaba |
|
2004 |
12 |
10 |
p. 2687-2690 4 p. |
artikel |
4 |
An o-nitrobenzyl scaffold for peptide ligation: synthesis and applications
|
Marinzi, Chiara |
|
2004 |
12 |
10 |
p. 2749-2757 9 p. |
artikel |
5 |
A predictive pharmacophore model of human melanocortin-4 receptor as derived from the solution structures of cyclic peptides
|
Sun, Hongmao |
|
2004 |
12 |
10 |
p. 2671-2677 7 p. |
artikel |
6 |
Binding of an influenza A virus to a neomembrane measured by surface plasmon resonance
|
Critchley, Peter |
|
2004 |
12 |
10 |
p. 2773-2780 8 p. |
artikel |
7 |
Binding of tryptamine analogs at h5-HT1E receptors: a structure–affinity investigation
|
Dukat, Małgorzata |
|
2004 |
12 |
10 |
p. 2545-2552 8 p. |
artikel |
8 |
Carbonic anhydrase inhibitors: aromatic and heterocyclic sulfonamides incorporating adamantyl moieties with strong anticonvulsant activity
|
Ilies, Marc A |
|
2004 |
12 |
10 |
p. 2717-2726 10 p. |
artikel |
9 |
Cinnamic amides of ( S )-2-(aminomethyl)pyrrolidines are potent H3 antagonists
|
Peschke, Bernd |
|
2004 |
12 |
10 |
p. 2603-2616 14 p. |
artikel |
10 |
Clozapine derived 2,3-dihydro-1H-1,4- and 1,5-benzodiazepines with D4 receptor selectivity: synthesis and biological testing
|
Hussenether, Thomas |
|
2004 |
12 |
10 |
p. 2625-2637 13 p. |
artikel |
11 |
Comparison of the dark and light-induced toxicity of thio and seleno analogues of the thiopyrylium dye AA1
|
Detty, Michael R |
|
2004 |
12 |
10 |
p. 2589-2596 8 p. |
artikel |
12 |
Contributors to this issue
|
|
|
2004 |
12 |
10 |
p. I- 1 p. |
artikel |
13 |
Differential effects of synthesized 2′-oxygenated chalcone derivatives: modulation of human cell cycle phase distribution
|
Rao, Yerra Koteswara |
|
2004 |
12 |
10 |
p. 2679-2686 8 p. |
artikel |
14 |
3D-QSAR analysis of conformationally constrained diacylglycerol (DAG) analogues as potent protein kinase C (PK-C) ligands
|
Kim, Su Yeon |
|
2004 |
12 |
10 |
p. 2639-2644 6 p. |
artikel |
15 |
3D-QSAR CoMFA/CoMSIA studies on Urokinase plasminogen activator (uPA) inhibitors: a strategic design in novel anticancer agents
|
Bhongade, B.A. |
|
2004 |
12 |
10 |
p. 2797-2805 9 p. |
artikel |
16 |
3D-QSAR studies of pyruvate dehydrogenase kinase inhibitors based on a divide and conquer strategy
|
Aboye, Teshome Leta |
|
2004 |
12 |
10 |
p. 2709-2715 7 p. |
artikel |
17 |
Editorial board
|
|
|
2004 |
12 |
10 |
p. IFC- 1 p. |
artikel |
18 |
ERβ Ligands. Part 2: Synthesis and structure–activity relationships of a series of 4-hydroxy-biphenyl-carbaldehyde oxime derivatives
|
Yang, Cuijian |
|
2004 |
12 |
10 |
p. 2553-2570 18 p. |
artikel |
19 |
Fluorinated phenylcyclopropylamines. Part 3: Inhibition of monoamine oxidase A and B
|
Yoshida, Shinichi |
|
2004 |
12 |
10 |
p. 2645-2652 8 p. |
artikel |
20 |
Graphical contents list
|
|
|
2004 |
12 |
10 |
p. 2491-2499 9 p. |
artikel |
21 |
Instructions to contributors
|
|
|
2004 |
12 |
10 |
p. III-VII nvt p. |
artikel |
22 |
Naphtho[2,1-b][1,5] and [1,2-f][1,4]oxazocines as selective NK1 antagonists
|
Ohnmacht, Cyrus J. |
|
2004 |
12 |
10 |
p. 2653-2669 17 p. |
artikel |
23 |
Old drugs as lead compounds for a new disease? Binding analysis of SARS coronavirus main proteinase with HIV, psychotic and parasite drugs
|
Zhang, Xue Wu |
|
2004 |
12 |
10 |
p. 2517-2521 5 p. |
artikel |
24 |
Purification and partial amino acid sequences of the enzyme vinorine synthase involved in a crucial step of ajmaline biosynthesis
|
Gerasimenko, Irina |
|
2004 |
12 |
10 |
p. 2781-2786 6 p. |
artikel |
25 |
Ring-substituted quinolines as potential anti-tuberculosis agents
|
Vangapandu, Suryanarayana |
|
2004 |
12 |
10 |
p. 2501-2508 8 p. |
artikel |
26 |
S1 subsite in snake venom thrombin-like enzymes: can S1 subsite lipophilicity be used to sort binding affinities of trypsin-like enzymes to small-molecule inhibitors?
|
Silva Jr., Floriano P. |
|
2004 |
12 |
10 |
p. 2571-2587 17 p. |
artikel |
27 |
Structural variations of 1-(4-(phenoxymethyl)benzyl)piperidines as nonimidazole histamine H3 receptor antagonists
|
Mikó, Tibor |
|
2004 |
12 |
10 |
p. 2727-2736 10 p. |
artikel |
28 |
Synthesis and activity of 1H-benzimidazole and 1H-benzotriazole derivatives as inhibitors of Acanthamoeba castellanii
|
Kopańska (née Zastąpiło), Katarzyna |
|
2004 |
12 |
10 |
p. 2617-2624 8 p. |
artikel |
29 |
Synthesis and pharmacological properties of benzamide derivatives as selective serotonin 4 receptor agonists
|
Sonda, Shuji |
|
2004 |
12 |
10 |
p. 2737-2747 11 p. |
artikel |
30 |
Synthesis and structure activity relationship of guanidines as NPY Y5 antagonists
|
Aquino, Christopher J |
|
2004 |
12 |
10 |
p. 2691-2708 18 p. |
artikel |
31 |
Synthesis, cytotoxicity, QSAR, and intercalation study of new diindenopyridine derivatives
|
Miri, Ramin |
|
2004 |
12 |
10 |
p. 2529-2536 8 p. |
artikel |
32 |
Synthesis, in vitro and in vivo activity of benzophenone-based inhibitors of steroid sulfatase
|
Hejaz, Hatem A.M |
|
2004 |
12 |
10 |
p. 2759-2772 14 p. |
artikel |
33 |
Synthesis of anticancer β-lactams: mechanism of action
|
Banik, Bimal K. |
|
2004 |
12 |
10 |
p. 2523-2528 6 p. |
artikel |
34 |
Synthesis, properties, and photodynamic properties in vitro of heavy-chalcogen analogues of tetramethylrosamine
|
Detty, Michael R |
|
2004 |
12 |
10 |
p. 2537-2544 8 p. |
artikel |
35 |
Taxol derivatives are selective inhibitors of DNA polymerase α
|
Oshige, Masahiko |
|
2004 |
12 |
10 |
p. 2597-2601 5 p. |
artikel |