nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A model for identifying HERG K+ channel blockers
|
Aronov, Alex M. |
|
2004 |
12 |
9 |
p. 2307-2315 9 p. |
artikel |
2 |
Baylis–Hillman reaction assisted parallel synthesis of 3,5-disubstituted isoxazoles and their in vivo bioevaluation as antithrombotic agents
|
Batra, S. |
|
2004 |
12 |
9 |
p. 2059-2077 19 p. |
artikel |
3 |
CCR5 antagonists as anti-HIV-1 agents. Part 2: Synthesis and biological evaluation of N-[3-(4-benzylpiperidin-1-yl)propyl]-N,N ′-diphenylureas
|
Imamura, Shinichi |
|
2004 |
12 |
9 |
p. 2295-2306 12 p. |
artikel |
4 |
Chloroalkyl piperazine and nitrogen mustard porphyrins: synthesis and anticancer activity
|
Guo, Can-Cheng |
|
2004 |
12 |
9 |
p. 2469-2475 7 p. |
artikel |
5 |
C17,20-Lyase inhibitors I. Structure-based de novo design and SAR study of C17,20-lyase inhibitors
|
Matsunaga, Nobuyuki |
|
2004 |
12 |
9 |
p. 2251-2273 23 p. |
artikel |
6 |
α-C-Mannosyltryptophan is not recognized by conventional mannose-binding lectins
|
Nishikawa, Toshio |
|
2004 |
12 |
9 |
p. 2343-2348 6 p. |
artikel |
7 |
Coaggregate of amphiphilic zinc chlorins with synthetic surfactants in an aqueous medium to an artificial supramolecular light-harvesting system
|
Miyatake, Tomohiro |
|
2004 |
12 |
9 |
p. 2173-2178 6 p. |
artikel |
8 |
Contributors to this issue
|
|
|
2004 |
12 |
9 |
p. I-II nvt p. |
artikel |
9 |
Corrigendum to “Photo-induced DNA cleavage reaction characteristics of propargylic sulfones possessing anthraquinone chromophore”
|
Haruna, Ken-ichi |
|
2004 |
12 |
9 |
p. 2489- 1 p. |
artikel |
10 |
C(8)-Substituted 1-azabicyclo[3.3.1]non-3-enes: a novel scaffold for muscarinic receptor ligands
|
Goo Kim, Myoung |
|
2004 |
12 |
9 |
p. 2357-2367 11 p. |
artikel |
11 |
Cytotoxicity of phenylpropanoid esters from the stems of Hibiscus taiwanensis
|
Wu, Pei-Lin |
|
2004 |
12 |
9 |
p. 2193-2197 5 p. |
artikel |
12 |
De novo design and synthesis of HIV-1 integrase inhibitors
|
Makhija, Mahindra T |
|
2004 |
12 |
9 |
p. 2317-2333 17 p. |
artikel |
13 |
Design and synthesis of Rho kinase inhibitors (I)
|
Takami, Atsuya |
|
2004 |
12 |
9 |
p. 2115-2137 23 p. |
artikel |
14 |
Design, synthesis and biological activity of amidinobicyclic compounds (derivatives of DX-9065a) as factor Xa inhibitors: SAR study of S1 and aryl binding sites
|
Komoriya, Satoshi |
|
2004 |
12 |
9 |
p. 2099-2114 16 p. |
artikel |
15 |
Design, synthesis, and biological evaluation of novel 2-pyridinyl-[1,2,4]triazoles as inhibitors of transforming growth factor β1 type 1 receptor
|
Kim, Dae-Kee |
|
2004 |
12 |
9 |
p. 2013-2020 8 p. |
artikel |
16 |
Editorial board
|
|
|
2004 |
12 |
9 |
p. IFC- 1 p. |
artikel |
17 |
Elucidating inhibitory models of the inhibitors of epidermal growth factor receptor by docking and 3D-QSAR
|
Chen, Gang |
|
2004 |
12 |
9 |
p. 2409-2417 9 p. |
artikel |
18 |
Exploring distal regions of the A3 adenosine receptor binding site: sterically constrained N 6-(2-phenylethyl)adenosine derivatives as potent ligands
|
Tchilibon, Susanna |
|
2004 |
12 |
9 |
p. 2021-2034 14 p. |
artikel |
19 |
Exploring the binding mechanism of the main proteinase in SARS-associated coronavirus and its implication to anti-SARS drug design
|
Zhang, Xue Wu |
|
2004 |
12 |
9 |
p. 2219-2223 5 p. |
artikel |
20 |
Graphical contents list
|
|
|
2004 |
12 |
9 |
p. 1971-1982 12 p. |
artikel |
21 |
Homology modeling and molecular dynamics studies of a novel C3-like ADP-ribosyltransferase
|
Xiao, Jing-fa |
|
2004 |
12 |
9 |
p. 2035-2041 7 p. |
artikel |
22 |
Influence of stereoisomer of dispiro-1,2,4,5-tetraoxanes on their binding mode with heme and on antimalarial activity: molecular docking studies
|
Tonmunphean, Somsak |
|
2004 |
12 |
9 |
p. 2005-2012 8 p. |
artikel |
23 |
Instructions to contributors
|
|
|
2004 |
12 |
9 |
p. III-VII nvt p. |
artikel |
24 |
Kinetics and structure–activity relationship studies on pregnane-type steroidal alkaloids that inhibit cholinesterases
|
Khalid, Asaad |
|
2004 |
12 |
9 |
p. 1995-2003 9 p. |
artikel |
25 |
LNA guanine and 2,6-diaminopurine. Synthesis, characterization and hybridization properties of LNA 2,6-diaminopurine containing oligonucleotides
|
Rosenbohm, Christoph |
|
2004 |
12 |
9 |
p. 2385-2396 12 p. |
artikel |
26 |
N-Aroyloxylthioxo-naphthalimides as DNA photocleavers of aroyloxyl oxygen radicals: synthesis, evaluation, and substituents’ effect
|
Xu, Yufang |
|
2004 |
12 |
9 |
p. 2335-2341 7 p. |
artikel |
27 |
New N-arylsulfonyl-N-alkoxyaminoacetohydroxamic acids as selective inhibitors of gelatinase A (MMP-2)
|
Rossello, Armando |
|
2004 |
12 |
9 |
p. 2441-2450 10 p. |
artikel |
28 |
Optically active antifungal azoles: synthesis and antifungal activity of (2R,3S)-2-(2,4-difluorophenyl)-3-(5-{2-[4-aryl-piperazin-1-yl]-ethyl}-tetrazol-2-yl/1-yl)-1-[1,2,4]-triazol-1-yl-butan-2-ol
|
Upadhayaya, Ram Shankar |
|
2004 |
12 |
9 |
p. 2225-2238 14 p. |
artikel |
29 |
Potent and orally active ETA selective antagonists with 5,7-diarylcyclopenteno[1,2-b]pyridine-6-carboxylic acid structures
|
Yoshizumi, Takashi |
|
2004 |
12 |
9 |
p. 2139-2150 12 p. |
artikel |
30 |
Potential therapeutic antioxidants that combine the radical scavenging ability of myricetin and the lipophilic chain of vitamin E to effectively inhibit microsomal lipid peroxidation
|
Bennett, Christopher J. |
|
2004 |
12 |
9 |
p. 2079-2098 20 p. |
artikel |
31 |
QSAR study on CA inhibitory activity of disulfonamides: effect of halogen substitution
|
Jaiswal, Mona |
|
2004 |
12 |
9 |
p. 2477-2482 6 p. |
artikel |
32 |
QSAR study on phenolic activity: need of positive hydrophobic term (logP) in QSAR
|
Thakur, Mamta |
|
2004 |
12 |
9 |
p. 2287-2293 7 p. |
artikel |
33 |
Solution structure of rifaximin and its synthetic derivative rifaximin OR determined by experimental NMR and theoretical simulation methods
|
Martini, Silvia |
|
2004 |
12 |
9 |
p. 2163-2172 10 p. |
artikel |
34 |
Structural effects on the reactivity 1,4-dihydropyridines with alkylperoxyl radicals and ABTS radical cation
|
Yáñez, C |
|
2004 |
12 |
9 |
p. 2459-2468 10 p. |
artikel |
35 |
Structure–activity relationships of epolactaene analogs as DNA polymerases inhibitors
|
Kuramochi, Kouji |
|
2004 |
12 |
9 |
p. 1983-1989 7 p. |
artikel |
36 |
Study of the interactions between tetracycline analogues and lysozyme
|
Jiang, Chong-qiu |
|
2004 |
12 |
9 |
p. 2043-2047 5 p. |
artikel |
37 |
Sulfamide derivatives as transition state analogue inhibitors for carboxypeptidase A
|
Park, Jung Dae |
|
2004 |
12 |
9 |
p. 2349-2356 8 p. |
artikel |
38 |
Syntheses and DNA-binding studies of a series of unsymmetrical cyanine dyes: structural influence on the degree of minor groove binding to natural DNA
|
Karlsson, H.Jonas |
|
2004 |
12 |
9 |
p. 2369-2384 16 p. |
artikel |
39 |
Synthesis and biological activities of some new dibenzopyranones and dibenzopyrans: search for potential oestrogen receptor agonists and antagonists
|
Pandey, Jaya |
|
2004 |
12 |
9 |
p. 2239-2249 11 p. |
artikel |
40 |
Synthesis and biological activity of novel 1,4-diazepane derivatives as factor Xa inhibitor with potent anticoagulant and antithrombotic activity
|
Koshio, Hiroyuki |
|
2004 |
12 |
9 |
p. 2179-2191 13 p. |
artikel |
41 |
Synthesis and biological activity of novel α-substituted β-phenylpropionic acids having pyridin-2-ylphenyl moiety as antihyperglycemic agents
|
Takamura, Makoto |
|
2004 |
12 |
9 |
p. 2419-2439 21 p. |
artikel |
42 |
Synthesis and cytotoxic activity of novel quinazolino-β-carboline-5-one derivatives
|
Baruah, Bipul |
|
2004 |
12 |
9 |
p. 1991-1994 4 p. |
artikel |
43 |
Synthesis and evaluation of some new spiro indoline-based heterocycles as potentially active antimicrobial agents
|
Abdel-Rahman, A.H. |
|
2004 |
12 |
9 |
p. 2483-2488 6 p. |
artikel |
44 |
Synthesis and immunomodulatory properties of selected oxazolone derivatives
|
Mesaik, Muhammad A |
|
2004 |
12 |
9 |
p. 2049-2057 9 p. |
artikel |
45 |
Synthesis and preliminary evaluation of some pyrazine containing thiazolines and thiazolidinones as antimicrobial agents
|
Bonde, Chandrakant G. |
|
2004 |
12 |
9 |
p. 2151-2161 11 p. |
artikel |
46 |
Synthesis and structure–activity relationships of thioflavone derivatives as specific inhibitors of the ERK-MAP kinase signaling pathway
|
Kataoka, Tadashi |
|
2004 |
12 |
9 |
p. 2397-2407 11 p. |
artikel |
47 |
Synthesis, biological evaluation and molecular modelling of diversely functionalized heterocyclic derivatives as inhibitors of acetylcholinesterase/butyrylcholinesterase and modulators of Ca2+ channels and nicotinic receptors
|
Marco, José L |
|
2004 |
12 |
9 |
p. 2199-2218 20 p. |
artikel |
48 |
Synthesis of dihydronaphthofurandiones and dihydrofuroquinolinediones with trypanocidal activity and analysis of their stereoelectronic properties
|
Tapia, Ricardo A. |
|
2004 |
12 |
9 |
p. 2451-2458 8 p. |
artikel |
49 |
The composition and sequence specificity of Pro-Ala-Lys-OH for the thrombolytic activities of P6A and related oligopeptides
|
Zhao, Ming |
|
2004 |
12 |
9 |
p. 2275-2286 12 p. |
artikel |