| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Additional level of information about complex interaction between non-nucleoside inhibitor and HIV-1 reverse transcriptase using biosensor-based thermodynamic analysis
|
Geitmann, Matthis
|
|
2007
|
15 |
23 |
p. 7344-7354
11 p.
|
artikel
|
| 2 |
Carbonic anhydrase inhibitors: Cloning, characterization, and inhibition studies of the cytosolic isozyme III with sulfonamides
|
Nishimori, Isao
|
|
2007
|
15 |
23 |
p. 7229-7236
8 p.
|
artikel
|
| 3 |
Click chemistry based solid phase supported synthesis of dopaminergic phenylacetylenes
|
Rodriguez Loaiza, Pilar
|
|
2007
|
15 |
23 |
p. 7248-7257
10 p.
|
artikel
|
| 4 |
Construction of polyamine-modified uridine and adenosine derivatives—evaluation of DNA binding capacity and cytotoxicity in vitro
|
Ghatnekar, Johannes
|
|
2007
|
15 |
23 |
p. 7426-7433
8 p.
|
artikel
|
| 5 |
Corrigendum to ‘Synthesis, characterization and antimicrobial activity of new aliphatic sulfonamide’
|
Özbek, Neslihan
|
|
2007
|
15 |
23 |
p. 7494-
1 p.
|
artikel
|
| 6 |
Direct diazo-transfer reaction on β-lactam: Synthesis and preliminary biological activities of 6-triazolylpenicillanic acids
|
Chen, Po C.
|
|
2007
|
15 |
23 |
p. 7288-7300
13 p.
|
artikel
|
| 7 |
Discovery of 1,1-dioxo-1,2,6-thiadiazine-5-carboxamide derivatives as cannabinoid-like molecules with agonist and antagonist activity
|
Cano, Carolina
|
|
2007
|
15 |
23 |
p. 7480-7493
14 p.
|
artikel
|
| 8 |
Editorial board
|
|
|
2007
|
15 |
23 |
p. IFC-
1 p.
|
artikel
|
| 9 |
Efficient one-pot synthesis of biologically active polysubstituted aromatic amines
|
Menche, Dirk
|
|
2007
|
15 |
23 |
p. 7311-7317
7 p.
|
artikel
|
| 10 |
Graphical contents list
|
|
|
2007
|
15 |
23 |
p. 7221-7228
8 p.
|
artikel
|
| 11 |
Hybrid approach for the design of highly affine and selective dopamine D3 receptor ligands using privileged scaffolds of biogenic amine GPCR ligands
|
Sasse, Britta C.
|
|
2007
|
15 |
23 |
p. 7258-7273
16 p.
|
artikel
|
| 12 |
Identification of a series of novel derivatives as potent HCV inhibitors by a ligand-based virtual screening optimized procedure
|
Melagraki, Georgia
|
|
2007
|
15 |
23 |
p. 7237-7247
11 p.
|
artikel
|
| 13 |
Instructions to contributors
|
|
|
2007
|
15 |
23 |
p. I-
1 p.
|
artikel
|
| 14 |
Mimetics of the tri- and tetrasaccharide epitope of GQ1bα as myelin-associated glycoprotein (MAG) ligands
|
Gao, Ganpan
|
|
2007
|
15 |
23 |
p. 7459-7469
11 p.
|
artikel
|
| 15 |
Molecular probe for enzymatic activity with dual output
|
Danieli, Eyal
|
|
2007
|
15 |
23 |
p. 7318-7324
7 p.
|
artikel
|
| 16 |
Natural triterpenoids from Cecropia lyratiloba are cytotoxic to both sensitive and multidrug resistant leukemia cell lines
|
Rocha, Gleice da Graça
|
|
2007
|
15 |
23 |
p. 7355-7360
6 p.
|
artikel
|
| 17 |
New functional assay of P-glycoprotein activity using Hoechst 33342
|
Müller, Henrik
|
|
2007
|
15 |
23 |
p. 7470-7479
10 p.
|
artikel
|
| 18 |
Phenylimidazole derivatives as specific inhibitors of bacterial enoyl-acyl carrier protein reductase FabK
|
Ozawa, Tomohiro
|
|
2007
|
15 |
23 |
p. 7325-7336
12 p.
|
artikel
|
| 19 |
[(2-Phenylindol-3-yl)methylene]propanedinitriles inhibit the growth of breast cancer cells by cell cycle arrest in G2/M phase and apoptosis
|
Pojarová, Michaela
|
|
2007
|
15 |
23 |
p. 7368-7379
12 p.
|
artikel
|
| 20 |
Rational design, synthesis and evaluation of (6aR ∗,11bS ∗)-1-(4-fluorophenyl)-4-{7-[4-(4-fluorophenyl)-4-oxobutyl]1,2,3,4,6,6a,7,11b,12,12a(RS)-decahydropyrazino[2′,1′:6,1]pyrido[3,4-b]indol-2-yl}-butan-1-one as a potential neuroleptic agent
|
Chakrabarty, Ruchika
|
|
2007
|
15 |
23 |
p. 7361-7367
7 p.
|
artikel
|
| 21 |
Structure–activity relationship of antileishmanials neolignan analogues
|
Aveniente, Mário
|
|
2007
|
15 |
23 |
p. 7337-7343
7 p.
|
artikel
|
| 22 |
Structure–activity relationship studies of flavonoids as potent inhibitors of human platelet 12-hLO, reticulocyte 15-hLO-1, and prostate epithelial 15-hLO-2
|
Vasquez-Martinez, Yesseny
|
|
2007
|
15 |
23 |
p. 7408-7425
18 p.
|
artikel
|
| 23 |
Synthesis and biological evaluation of non-peptide αvβ3/α5β1 integrin dual antagonists containing 5,6-dihydropyridin-2-one scaffolds
|
Benfatti, Fides
|
|
2007
|
15 |
23 |
p. 7380-7390
11 p.
|
artikel
|
| 24 |
Synthesis and biological evaluation of norcantharidin analogues: Towards PP1 selectivity
|
Stewart, Scott G.
|
|
2007
|
15 |
23 |
p. 7301-7310
10 p.
|
artikel
|
| 25 |
Synthesis and screening for acetylcholinesterase inhibitor activity of some novel 2-butyl-1,3-diaza-spiro[4,4]non-1-en-4-ones: Derivatives of irbesartan key intermediate
|
Kavitha, C.V.
|
|
2007
|
15 |
23 |
p. 7391-7398
8 p.
|
artikel
|
| 26 |
Synthesis and structure–activity relationship of 7-(substituted)-aminomethyl-4-quinolone-3-carboxylic acid derivatives
|
Zhang, Zhenfa
|
|
2007
|
15 |
23 |
p. 7274-7280
7 p.
|
artikel
|
| 27 |
Synthesis, antifungal and antimycobacterial activities of new bis-imidazole derivatives, and prediction of their binding to P45014DM by molecular docking and MM/PBSA method
|
Zampieri, Daniele
|
|
2007
|
15 |
23 |
p. 7444-7458
15 p.
|
artikel
|
| 28 |
The antiviral drug ribavirin is a selective inhibitor of S-adenosyl-l-homocysteine hydrolase from Trypanosoma cruzi
|
Cai, Sumin
|
|
2007
|
15 |
23 |
p. 7281-7287
7 p.
|
artikel
|
| 29 |
The design and synthesis of N-1-alkylated-5-aminoaryalkylsubstituted-6-methyluracils as potential non-nucleoside HIV-1 RT inhibitors
|
Lu, Xiao
|
|
2007
|
15 |
23 |
p. 7399-7407
9 p.
|
artikel
|
| 30 |
The molecular pruning of a phosphoramidate peptidomimetic inhibitor of prostate-specific membrane antigen
|
Wu, Lisa Y.
|
|
2007
|
15 |
23 |
p. 7434-7443
10 p.
|
artikel
|
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