| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Amber force field implementation, molecular modelling study, synthesis and MMP-1/MMP-2 inhibition profile of (R)- and (S)-N-hydroxy-2-(N-isopropoxybiphenyl-4-ylsulfonamido)-3-methylbutanamides
|
Tuccinardi, Tiziano
|
|
2006
|
14 |
12 |
p. 4260-4276
17 p.
|
artikel
|
| 2 |
A new synthetic protocol for labeled oligonucleotides, using a chemically cleavable universal linker
|
Mahajan, Shweta
|
|
2006
|
14 |
12 |
p. 4302-4309
8 p.
|
artikel
|
| 3 |
Baicalein is a potent in vitro inhibitor against both reticulocyte 15-human and platelet 12-human lipoxygenases
|
Deschamps, Joshua D.
|
|
2006
|
14 |
12 |
p. 4295-4301
7 p.
|
artikel
|
| 4 |
Binding of actinomycin C1 (D) and actinomin to base-modified oligonucleotide duplexes with parallel chain orientation
|
Li, Hong
|
|
2006
|
14 |
12 |
p. 4089-4100
12 p.
|
artikel
|
| 5 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2006
|
14 |
12 |
p. 4310-4312
3 p.
|
artikel
|
| 6 |
Correlation of the acid-sensitivity of polyethylene glycol daunorubicin conjugates with their in vitro antiproliferative activity
|
Rodrigues, Paula C.A.
|
|
2006
|
14 |
12 |
p. 4110-4117
8 p.
|
artikel
|
| 7 |
Discovery of a new chemical lead for a matrix metalloproteinase inhibitor
|
Ikura, Masahiro
|
|
2006
|
14 |
12 |
p. 4241-4252
12 p.
|
artikel
|
| 8 |
Editorial Board
|
|
|
2006
|
14 |
12 |
p. CO2-
1 p.
|
artikel
|
| 9 |
Graphical contents list
|
|
|
2006
|
14 |
12 |
p. 3979-3986
8 p.
|
artikel
|
| 10 |
In silico ADME modelling 2: Computational models to predict human serum albumin binding affinity using ant colony systems
|
Gunturi, Sitarama B.
|
|
2006
|
14 |
12 |
p. 4118-4129
12 p.
|
artikel
|
| 11 |
Instructions to contributors
|
|
|
2006
|
14 |
12 |
p. I-
1 p.
|
artikel
|
| 12 |
Isoxazole-type derivatives related to combretastatin A-4, synthesis and biological evaluation
|
Kaffy, Julia
|
|
2006
|
14 |
12 |
p. 4067-4077
11 p.
|
artikel
|
| 13 |
Linear and nonlinear QSAR study of N-hydroxy-2-[(phenylsulfonyl)amino]acetamide derivatives as matrix metalloproteinase inhibitors
|
Fernández, Michael
|
|
2006
|
14 |
12 |
p. 4137-4150
14 p.
|
artikel
|
| 14 |
Monometallic complexes of 1,4,7,10-tetraazacyclododecane containing an imidazolium side: Synthesis, characterization, and their interaction with plasmid DNA
|
Li, Qiang-Lin
|
|
2006
|
14 |
12 |
p. 4151-4157
7 p.
|
artikel
|
| 15 |
New derivatives of xanthenone-4-acetic acid: Synthesis, pharmacological profile and effect on TNF-α and NO production by human immune cells
|
Gobbi, Silvia
|
|
2006
|
14 |
12 |
p. 4101-4109
9 p.
|
artikel
|
| 16 |
β-Nitrostyrene derivatives as potential antibacterial agents: A structure–property–activity relationship study
|
Milhazes, Nuno
|
|
2006
|
14 |
12 |
p. 4078-4088
11 p.
|
artikel
|
| 17 |
Photodynamic inactivation of Escherichia coli immobilized on agar surfaces by a tricationic porphyrin
|
Caminos, Daniel A.
|
|
2006
|
14 |
12 |
p. 4253-4259
7 p.
|
artikel
|
| 18 |
Preparation of antibodies against a novel immunosuppressant, FTY720, and development of an enzyme immunoassay for FTY720
|
Matsumoto, Norimasa
|
|
2006
|
14 |
12 |
p. 4182-4192
11 p.
|
artikel
|
| 19 |
Prodrugs of 3-(3,4-dichlorobenzyloxy)-2-amino-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid (MGS0039): A potent and orally active group II mGluR antagonist with antidepressant-like potential
|
Yasuhara, Akito
|
|
2006
|
14 |
12 |
p. 4193-4207
15 p.
|
artikel
|
| 20 |
Quantitative 31P NMR detection of oxygen-centered and carbon-centered radical species
|
Argyropoulos, Dimitris S.
|
|
2006
|
14 |
12 |
p. 4017-4028
12 p.
|
artikel
|
| 21 |
Recent developments in the identification of novel oxazolidinone antibacterial agents
|
Renslo, Adam R.
|
|
2006
|
14 |
12 |
p. 4227-4240
14 p.
|
artikel
|
| 22 |
Selection of a 2-azabicyclo[2.2.2]octane-based α4β1 integrin antagonist as an inhaled anti-asthmatic agent
|
Lawson, Edward C.
|
|
2006
|
14 |
12 |
p. 4208-4216
9 p.
|
artikel
|
| 23 |
Spirocyclopropyl pyrrolidines as a new series of α-l-fucosidase inhibitors
|
Laroche, Christophe
|
|
2006
|
14 |
12 |
p. 4047-4054
8 p.
|
artikel
|
| 24 |
Structure basis for the inhibitory mechanism of a novel DNase γ-specific inhibitor, DR396
|
Sunaga, Satoshi
|
|
2006
|
14 |
12 |
p. 4217-4226
10 p.
|
artikel
|
| 25 |
Synthesis and biological activities of new 1α,25-dihydroxy-19-norvitamin D3 analogs with modifications in both the A-ring and the side chain
|
Shimizu, Masato
|
|
2006
|
14 |
12 |
p. 4277-4294
18 p.
|
artikel
|
| 26 |
Synthesis and biological activity of isoprenoid bisphosphonates
|
Shull, Larry W.
|
|
2006
|
14 |
12 |
p. 4130-4136
7 p.
|
artikel
|
| 27 |
Synthesis and in vivo evaluation of [11C]SN003 as a PET ligand for CRF1 receptors
|
Kumar, J.S. Dileep
|
|
2006
|
14 |
12 |
p. 4029-4034
6 p.
|
artikel
|
| 28 |
Synthesis, antiviral activity, and pharmacokinetic evaluation of P3 pyridylmethyl analogs of oximinoarylsulfonyl HIV-1 protease inhibitors
|
Randolph, John T.
|
|
2006
|
14 |
12 |
p. 4035-4046
12 p.
|
artikel
|
| 29 |
Synthesis, labeling, and biological evaluation of halogenated 2-quinolinecarboxamides as potential radioligands for the visualization of peripheral benzodiazepine receptors
|
Cappelli, Andrea
|
|
2006
|
14 |
12 |
p. 4055-4066
12 p.
|
artikel
|
| 30 |
Tetrahydropyrrolo[3,2-c]azepin-4-ones as a new class of cytotoxic compounds
|
Martínez, Roberto
|
|
2006
|
14 |
12 |
p. 4007-4016
10 p.
|
artikel
|
| 31 |
The purines: Potent and versatile small molecule inhibitors and modulators of key biological targets
|
Legraverend, Michel
|
|
2006
|
14 |
12 |
p. 3987-4006
20 p.
|
artikel
|
| 32 |
Tricyclic pharmacophore-based molecules as novel integrin αvβ3 antagonists. Part IV: Preliminary control of αvβ3 selectivity by meta-oriented substitution
|
Kubota, Dai
|
|
2006
|
14 |
12 |
p. 4158-4181
24 p.
|
artikel
|
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