| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Allosteric interactions and QSAR: On the role of ligand hydrophobicity
|
Hansch, Corwin
|
|
2003
|
11 |
9 |
p. 2075-2084
10 p.
|
artikel
|
| 2 |
Antiplatelet properties of novel N-substituted-phenyl-1,2,3-triazole-4-acylhydrazone derivatives
|
Cunha, Anna C.
|
|
2003
|
11 |
9 |
p. 2051-2059
9 p.
|
artikel
|
| 3 |
A quantitative structure–activity relationship study of hydroxamate matrix metalloproteinase inhibitors derived from funtionalized 4-aminoprolines
|
Gupta, S.P.
|
|
2003
|
11 |
9 |
p. 1975-1981
7 p.
|
artikel
|
| 4 |
Design and synthesis of broad-Based mono- and bi- cyclic inhibitors of FIV and HIV proteases
|
Mak, Chi Ching
|
|
2003
|
11 |
9 |
p. 2025-2040
16 p.
|
artikel
|
| 5 |
Design, synthesis and structure–Activity relationships of dual inhibitors of acetylcholinesterase and serotonin transporter as potential agents for Alzheimer's disease
|
Toda, Narihiro
|
|
2003
|
11 |
9 |
p. 1935-1955
21 p.
|
artikel
|
| 6 |
Directed evolution of N-acetylneuraminic acid aldolase to catalyze enantiomeric aldol reactions
|
Wada, Masaru
|
|
2003
|
11 |
9 |
p. 2091-2098
8 p.
|
artikel
|
| 7 |
Editorial board
|
|
|
2003
|
11 |
9 |
p. IFC-
1 p.
|
artikel
|
| 8 |
Graphical Abstracts
|
|
|
2003
|
11 |
9 |
p. 1929-1933
5 p.
|
artikel
|
| 9 |
5H-Dibenzo[c,h]1,6-naphthyridin-6-ones: novel topoisomerase I-Targeting anticancer agents with potent cytotoxic activity
|
Ruchelman, Alexander L.
|
|
2003
|
11 |
9 |
p. 2061-2073
13 p.
|
artikel
|
| 10 |
Hydroxyl-Substituted sulfonylureas as potent inhibitors of specific [3H]Glyburide binding to rat brain synaptosomes
|
Hill, Ronald A.
|
|
2003
|
11 |
9 |
p. 2099-2113
15 p.
|
artikel
|
| 11 |
New thioderivatives of gossypol and gossypolone, as prodrugs of cytotoxic agents
|
Dao, Vi-Thuy
|
|
2003
|
11 |
9 |
p. 2001-2006
6 p.
|
artikel
|
| 12 |
Probing the activation site of ribonuclease L with new N 6-substituted 2′,5′-adenylate trimers
|
Münch, Ursula
|
|
2003
|
11 |
9 |
p. 2041-2049
9 p.
|
artikel
|
| 13 |
Pyridoacridine Alkaloids Inducing Neuronal Differentiation in a Neuroblastoma Cell Line, from Marine Sponge Biemna fortis
|
Aoki, Shunji
|
|
2003
|
11 |
9 |
p. 1969-1973
5 p.
|
artikel
|
| 14 |
QSAR studies in substituted 1,2,3,4,6,7,12,12a-octa-hydropyrazino[2′,1′:6,1]pyrido[3,4-b]indoles—a potent class of neuroleptics
|
Saxena, Anil K.
|
|
2003
|
11 |
9 |
p. 2085-2090
6 p.
|
artikel
|
| 15 |
QSAR study of quinolinediones with inhibitory activity of endothelium-Dependent vasorelaxation by CoMSIA
|
Choo, Hea-Young Park
|
|
2003
|
11 |
9 |
p. 2019-2023
5 p.
|
artikel
|
| 16 |
Structural Requirements of Flavonoids for Nitric Oxide Production Inhibitory Activity and Mechanism of Action
|
Matsuda, Hisashi
|
|
2003
|
11 |
9 |
p. 1995-2000
6 p.
|
artikel
|
| 17 |
Structural studies of [2′,6′-dimethyl-l-tyrosine1]endomorphin-2 analogues: enhanced activity and cis orientation of the Dmt-Pro amide bond
|
Okada, Yoshio
|
|
2003
|
11 |
9 |
p. 1983-1994
12 p.
|
artikel
|
| 18 |
Synthesis of (3,4) β-Methylenecepham and (3,4) β-Methylene-carbacepham via intramolecular carbene addition to double bond
|
Korda, Anna
|
|
2003
|
11 |
9 |
p. 1957-1967
11 p.
|
artikel
|
| 19 |
Tricyclic quinoxalines as potent kinase inhibitors of PDGFR kinase, Flt3 and Kit
|
Gazit, Aviv
|
|
2003
|
11 |
9 |
p. 2007-2018
12 p.
|
artikel
|
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