| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Antimalarial activity enhancement in hydroxymethylcarbonyl (HMC) isostere-based dipeptidomimetics targeting malarial aspartic protease plasmepsin
|
Hidaka, Koushi
|
|
2008
|
16 |
23 |
p. 10049-10060
12 p.
|
artikel
|
| 2 |
Antiobesity designed multiple ligands: Synthesis of pyrazole fatty acid amides and evaluation as hypophagic agents
|
Alvarado, Mario
|
|
2008
|
16 |
23 |
p. 10098-10105
8 p.
|
artikel
|
| 3 |
Computational design of novel fullerene analogues as potential HIV-1 PR inhibitors: Analysis of the binding interactions between fullerene inhibitors and HIV-1 PR residues using 3D QSAR, molecular docking and molecular dynamics simulations
|
Durdagi, Serdar
|
|
2008
|
16 |
23 |
p. 9957-9974
18 p.
|
artikel
|
| 4 |
Design and synthesis of novel 2′,3′-dideoxy-4′-selenonucleosides as potential antiviral agents
|
Jeong, Lak Shin
|
|
2008
|
16 |
23 |
p. 9891-9897
7 p.
|
artikel
|
| 5 |
Design, synthesis, and pharmacological evaluation of N-bicyclo-5-chloro-1H-indole-2-carboxamide derivatives as potent glycogen phosphorylase inhibitors
|
Onda, Kenichi
|
|
2008
|
16 |
23 |
p. 10001-10012
12 p.
|
artikel
|
| 6 |
Design, synthesis and preliminary pharmacological evaluation of new analogues of DM232 (unifiram) and DM235 (sunifiram) as cognition modulators
|
Martini, Elisabetta
|
|
2008
|
16 |
23 |
p. 10034-10042
9 p.
|
artikel
|
| 7 |
Discovery of new pyridoacridine alkaloids from Lissoclinum cf. badium that inhibit the ubiquitin ligase activity of Hdm2 and stabilize p53
|
Clement, Jason A.
|
|
2008
|
16 |
23 |
p. 10022-10028
7 p.
|
artikel
|
| 8 |
Editorial board
|
|
|
2008
|
16 |
23 |
p. IFC-
1 p.
|
artikel
|
| 9 |
Efficient synthesis and biological evaluation of two modafinil analogues
|
De Risi, Carmela
|
|
2008
|
16 |
23 |
p. 9904-9910
7 p.
|
artikel
|
| 10 |
Graphical contents list
|
|
|
2008
|
16 |
23 |
p. 9883-9890
8 p.
|
artikel
|
| 11 |
Hetero-Diels–Alder reaction of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with arylsulfonylcyanides. Synthesis and antimicrobial activity of 4-hydroxy-2-(arylsulfonyl)pyridines
|
Hussain, Ibrar
|
|
2008
|
16 |
23 |
p. 9898-9903
6 p.
|
artikel
|
| 12 |
Identification of 4-[1-[3-chloro-4-[N’-(5-fluoro-2-methylphenyl)ureido]phenylacetyl]-(4S)-fluoro-(2S)-pyrrolidinylmethoxy]benzoic acid as a potent, orally active VLA-4 antagonist
|
Muro, Fumihito
|
|
2008
|
16 |
23 |
p. 9991-10000
10 p.
|
artikel
|
| 13 |
Inhibition of aldose reductase from cataracted eye lenses by finger millet (Eleusine coracana) polyphenols
|
Chethan, S.
|
|
2008
|
16 |
23 |
p. 10085-10090
6 p.
|
artikel
|
| 14 |
Instructions to contributors
|
|
|
2008
|
16 |
23 |
p. I-
1 p.
|
artikel
|
| 15 |
Irreversible inhibition of dihydrodipicolinate synthase by 4-oxo-heptenedioic acid analogues
|
Boughton, Berin A.
|
|
2008
|
16 |
23 |
p. 9975-9983
9 p.
|
artikel
|
| 16 |
Novel azalides derived from 16-membered macrolides. Part II: Isolation of the linear 9-formylcarboxylic acid and its sequential macrocyclization with an amino alcohol or an azidoamine
|
Miura, Tomoaki
|
|
2008
|
16 |
23 |
p. 10129-10156
28 p.
|
artikel
|
| 17 |
Novel 3-phenylpropane-1,2-diamine derivates as inhibitors of aminopeptidase N (APN)
|
Shang, Luqing
|
|
2008
|
16 |
23 |
p. 9984-9990
7 p.
|
artikel
|
| 18 |
Photobactericidal plastic films based on cellulose esterified by chloroacetate and a cationic porphyrin
|
Krouit, Mohammed
|
|
2008
|
16 |
23 |
p. 10091-10097
7 p.
|
artikel
|
| 19 |
Poly(ADP-ribose) polymerase-1 activity facilitates the dissociation of nuclear proteins from platinum-modified DNA
|
Guggenheim, Evan R.
|
|
2008
|
16 |
23 |
p. 10121-10128
8 p.
|
artikel
|
| 20 |
Ratiometric multimodal chemosensors based on cubic silsesquioxanes for monitoring solvent polarity
|
Tanaka, Kazuo
|
|
2008
|
16 |
23 |
p. 10029-10033
5 p.
|
artikel
|
| 21 |
Search for α-helical propensity in the receptor-bound conformation of glucagon-like peptide-1
|
Murage, Eunice N.
|
|
2008
|
16 |
23 |
p. 10106-10112
7 p.
|
artikel
|
| 22 |
Structure and biological activity of novel FN analogs as flowering inducers
|
Kai, Kenji
|
|
2008
|
16 |
23 |
p. 10043-10048
6 p.
|
artikel
|
| 23 |
Substituted hippurates and hippurate analogs as substrates and inhibitors of peptidylglycine α-hydroxylating monooxygenase (PHM)
|
Merkler, David J.
|
|
2008
|
16 |
23 |
p. 10061-10074
14 p.
|
artikel
|
| 24 |
Synthesis and biological evaluation of guanylhydrazone coactivator binding inhibitors for the estrogen receptor
|
LaFrate, Andrew L.
|
|
2008
|
16 |
23 |
p. 10075-10084
10 p.
|
artikel
|
| 25 |
Synthesis and pharmacological evaluation of a second generation of pyridothiadiazine 1,1-dioxides acting as AMPA potentiators
|
Francotte, Pierre
|
|
2008
|
16 |
23 |
p. 9948-9956
9 p.
|
artikel
|
| 26 |
Synthesis and pharmacological evaluation of several ring-contracted amantadine analogs
|
Camps, Pelayo
|
|
2008
|
16 |
23 |
p. 9925-9936
12 p.
|
artikel
|
| 27 |
Synthesis and structure–activity relationships for biphenyl H3 receptor antagonists with moderate anti-cholinesterase activity
|
Morini, Giovanni
|
|
2008
|
16 |
23 |
p. 9911-9924
14 p.
|
artikel
|
| 28 |
The design, synthesis, and anti-tumor mechanism study of N-phosphoryl amino acid modified resveratrol analogues
|
Liu, Huachen
|
|
2008
|
16 |
23 |
p. 10013-10021
9 p.
|
artikel
|
| 29 |
Tyrosine-sulfate isosteres of CCR5 N-terminus as tools for studying HIV-1 entry
|
Lam, Son N.
|
|
2008
|
16 |
23 |
p. 10113-10120
8 p.
|
artikel
|
| 30 |
Using an aryl phenanthroimidazole moiety as a conjugated flexible intercalator to improve the hybridization efficiency of a triplex-forming oligonucleotide
|
Osman, Amany M.A.
|
|
2008
|
16 |
23 |
p. 9937-9947
11 p.
|
artikel
|
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