| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Anti-AIDS agents 84. Synthesis and anti-human immunodeficiency virus (HIV) activity of 2′-monomethyl-4-methyl- and 1′-thia-4-methyl-(3′R,4′R)-3′,4′-di-O-(S)-camphanoyl-(+)-cis-khellactone (DCK) analogs
|
Xu, Shi-Qing
|
|
2010
|
18 |
20 |
p. 7203-7211
9 p.
|
artikel
|
| 2 |
Design and preparation of sterol mimetics as potential antiparasitics
|
Gigante, Federica
|
|
2010
|
18 |
20 |
p. 7291-7301
11 p.
|
artikel
|
| 3 |
Design, synthesis, and evaluation of 5-methyl-4-phenoxy-5H-pyrrolo[3,2-d]pyrimidine derivatives: Novel VEGFR2 kinase inhibitors binding to inactive kinase conformation
|
Oguro, Yuya
|
|
2010
|
18 |
20 |
p. 7260-7273
14 p.
|
artikel
|
| 4 |
Design, synthesis, biological evaluation, and modeling of a non-carbohydrate antagonist of the myelin-associated glycoprotein
|
Schwardt, Oliver
|
|
2010
|
18 |
20 |
p. 7239-7251
13 p.
|
artikel
|
| 5 |
Diversity-oriented synthesis of cyclic acyldepsipeptides leads to the discovery of a potent antibacterial agent
|
Socha, Aaron M.
|
|
2010
|
18 |
20 |
p. 7193-7202
10 p.
|
artikel
|
| 6 |
Editorial board
|
|
|
2010
|
18 |
20 |
p. IFC-
1 p.
|
artikel
|
| 7 |
Graphical contents list
|
|
|
2010
|
18 |
20 |
p. 7145-7149
5 p.
|
artikel
|
| 8 |
Improvement of water-solubility of biarylcarboxylic acid peroxisome proliferator-activated receptor (PPAR) δ-selective partial agonists by disruption of molecular planarity/symmetry
|
Kasuga, Jun-ichi
|
|
2010
|
18 |
20 |
p. 7164-7173
10 p.
|
artikel
|
| 9 |
Intermolecular interaction and morphology investigation of drug loaded ABA-triblock copolymers with different hydrophilic/lipophilic ratios
|
Khoee, Sepideh
|
|
2010
|
18 |
20 |
p. 7283-7290
8 p.
|
artikel
|
| 10 |
N-Phenyl-N′-[4-(5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)phenyl]ureas as novel inhibitors of VEGFR and FGFR kinases
|
Oguro, Yuya
|
|
2010
|
18 |
20 |
p. 7150-7163
14 p.
|
artikel
|
| 11 |
Potential application of thymidylate kinase in nucleoside analogue activation in Plasmodium falciparum
|
Cui, Huaqing
|
|
2010
|
18 |
20 |
p. 7302-7309
8 p.
|
artikel
|
| 12 |
Quantitative structure–activity relationship studies of threo-methylphenidate analogs
|
Misra, Milind
|
|
2010
|
18 |
20 |
p. 7221-7238
18 p.
|
artikel
|
| 13 |
Synthesis and anti-HIV-1 evaluation of phosphonates which mimic the 5′-monophosphate of 4′-branched 2′,3′-didehydro-2′,3′-dideoxy nucleosides
|
Kubota, Yutaka
|
|
2010
|
18 |
20 |
p. 7186-7192
7 p.
|
artikel
|
| 14 |
Synthesis and biological evaluation of a series of aromatic bisphosphonates
|
Barney, Rocky J.
|
|
2010
|
18 |
20 |
p. 7212-7220
9 p.
|
artikel
|
| 15 |
Synthesis and evaluation of original amidoximes as antileishmanial agents
|
Bouhlel, Ahlem
|
|
2010
|
18 |
20 |
p. 7310-7320
11 p.
|
artikel
|
| 16 |
Synthesis, cytotoxicity and liposome preparation of 28-acetylenic betulin derivatives
|
Csuk, René
|
|
2010
|
18 |
20 |
p. 7252-7259
8 p.
|
artikel
|
| 17 |
Synthesis of a BSA-Lex glycoconjugate and recognition of Lex analogues by the anti-Lex monoclonal antibody SH1: The identification of a non-cross reactive analogue
|
Wang, Jo-Wen
|
|
2010
|
18 |
20 |
p. 7174-7185
12 p.
|
artikel
|
| 18 |
Synthesis of non-purine analogs of 6-aryl-9-benzylpurines, and their antimycobacterial activities. Compounds modified in the imidazole ring
|
Khoje, Abhijit Datta
|
|
2010
|
18 |
20 |
p. 7274-7282
9 p.
|
artikel
|
Tijdschrift beschrijving