| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Affinity purification and characterization of a key enzyme responsible for circadian rhythmic control of nyctinasty in Lespedeza cuneata L
|
Kato, Eisuke
|
|
2008
|
16 |
8 |
p. 4600-4616
17 p.
|
artikel
|
| 2 |
Antifungal and antimycobacterial activity of 1-(3,5-diaryl-4,5-dihydro-1H-pyrazol-4-yl)-1H-imidazole derivatives
|
Zampieri, Daniele
|
|
2008
|
16 |
8 |
p. 4516-4522
7 p.
|
artikel
|
| 3 |
Benzofused N-substituted cyclic enediynes: Activation and DNA-cleavage potential
|
Basak, Amit
|
|
2008
|
16 |
8 |
p. 4532-4537
6 p.
|
artikel
|
| 4 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2008
|
16 |
8 |
p. 4742-4744
3 p.
|
artikel
|
| 5 |
Co-existence of α-glucosidase-inhibitory and liver X receptor-regulatory activities and their separation by structural development
|
Dodo, Kosuke
|
|
2008
|
16 |
8 |
p. 4272-4285
14 p.
|
artikel
|
| 6 |
Computational modeling study of functional microdomains in cannabinoid receptor type 1
|
Gonzalez, Angel
|
|
2008
|
16 |
8 |
p. 4378-4389
12 p.
|
artikel
|
| 7 |
Degradation-promoters of cellular inhibitor of apoptosis protein 1 based on bestatin and actinonin
|
Sato, Shinichi
|
|
2008
|
16 |
8 |
p. 4685-4698
14 p.
|
artikel
|
| 8 |
Design and synthesis of nitrate esters of aromatic heterocyclic compounds as pharmacological preconditioning agents
|
Fotopoulou, Theano
|
|
2008
|
16 |
8 |
p. 4523-4531
9 p.
|
artikel
|
| 9 |
Design and synthesis of novel leucomycin analogues modified at the C-3 position. Part II: 3-O-(3-Aryl-2-propenyl)leucomycin analogues
|
Furuuchi, Takeshi
|
|
2008
|
16 |
8 |
p. 4401-4418
18 p.
|
artikel
|
| 10 |
Design, synthesis, and evaluation of trifluoromethyl ketones as inhibitors of SARS-CoV 3CL protease
|
Shao, Yi-Ming
|
|
2008
|
16 |
8 |
p. 4652-4660
9 p.
|
artikel
|
| 11 |
Design, synthesis and pharmacological evaluation of hybrid molecules out of quinazolinimines and lipoic acid lead to highly potent and selective butyrylcholinesterase inhibitors with antioxidant properties
|
Decker, Michael
|
|
2008
|
16 |
8 |
p. 4252-4261
10 p.
|
artikel
|
| 12 |
Discovery, synthesis and biological evaluation of isoquinolones as novel and highly selective JNK inhibitors (1)
|
Asano, Yasutomi
|
|
2008
|
16 |
8 |
p. 4715-4732
18 p.
|
artikel
|
| 13 |
Discovery, synthesis and biological evaluation of isoquinolones as novel and highly selective JNK inhibitors (2)
|
Asano, Yasutomi
|
|
2008
|
16 |
8 |
p. 4699-4714
16 p.
|
artikel
|
| 14 |
DNA threading bis(9-aminoacridine-4-carboxamides): Effects of piperidine sidechains on DNA binding, cytotoxicity and cell cycle arrest
|
He, Zhicong
|
|
2008
|
16 |
8 |
p. 4390-4400
11 p.
|
artikel
|
| 15 |
Editorial board
|
|
|
2008
|
16 |
8 |
p. IFC-
1 p.
|
artikel
|
| 16 |
Enantiospecific synthesis and cytotoxicity of 7-(4-methoxyphenyl)-6-phenyl-2,3,8,8a-tetrahydroindolizin-5(1H)-one enantiomers
|
Kimball, F. Scott
|
|
2008
|
16 |
8 |
p. 4367-4377
11 p.
|
artikel
|
| 17 |
Formation of fluorine-18 labeled diaryl ureas—labeled VEGFR-2/PDGFR dual inhibitors as molecular imaging agents for angiogenesis
|
Ilovich, O.
|
|
2008
|
16 |
8 |
p. 4242-4251
10 p.
|
artikel
|
| 18 |
Graphical contents list
|
|
|
2008
|
16 |
8 |
p. 4189-4202
14 p.
|
artikel
|
| 19 |
Identification of neomycin B-binding site in T box antiterminator model RNA
|
Anupam, Rajaneesh
|
|
2008
|
16 |
8 |
p. 4466-4470
5 p.
|
artikel
|
| 20 |
Identification of novel ligands for the RNA pseudoknot that regulate −1 ribosomal frameshifting
|
Park, So-Jung
|
|
2008
|
16 |
8 |
p. 4676-4684
9 p.
|
artikel
|
| 21 |
Inhibition of 15-lipoxygenase-catalysed oxygenation of arachidonic acid by substituted benzoic acids
|
Russell, Wendy R.
|
|
2008
|
16 |
8 |
p. 4589-4593
5 p.
|
artikel
|
| 22 |
Inhibitors of DNA polymerase β: Activity and mechanism
|
Gao, Zhijie
|
|
2008
|
16 |
8 |
p. 4331-4340
10 p.
|
artikel
|
| 23 |
Inhibitory effect of xanthones isolated from the pericarp of Garcinia mangostana L. on rat basophilic leukemia RBL-2H3 cell degranulation
|
Itoh, Tomohiro
|
|
2008
|
16 |
8 |
p. 4500-4508
9 p.
|
artikel
|
| 24 |
Instructions to contributors
|
|
|
2008
|
16 |
8 |
p. I-
1 p.
|
artikel
|
| 25 |
Internalisation of the μ-opioid receptor by endomorphin-1 and leu-enkephalin is dependant on aromatic amino acid residues
|
Del Borgo, Mark P.
|
|
2008
|
16 |
8 |
p. 4341-4346
6 p.
|
artikel
|
| 26 |
Investigating biological activity spectrum for novel quinoline analogues 2: Hydroxyquinolinecarboxamides with photosynthesis-inhibiting activity
|
Musiol, Robert
|
|
2008
|
16 |
8 |
p. 4490-4499
10 p.
|
artikel
|
| 27 |
Labeling, characterization, and in vivo localization of a new 90Y-based phosphonate chelate 2,3-dicarboxypropane-1,1-diphosphonic acid for the treatment of bone metastases: Comparison with 99mTc–DPD complex
|
Djokić, Divna Dj.
|
|
2008
|
16 |
8 |
p. 4457-4465
9 p.
|
artikel
|
| 28 |
Natural and non-natural prenylated chalcones: Synthesis, cytotoxicity and anti-oxidative activity
|
Vogel, Susanne
|
|
2008
|
16 |
8 |
p. 4286-4293
8 p.
|
artikel
|
| 29 |
NMR evaluation of adipocyte fatty acid binding protein (aP2) with R- and S-ibuprofen
|
Bai, Guoyun
|
|
2008
|
16 |
8 |
p. 4323-4330
8 p.
|
artikel
|
| 30 |
Novel 3-aroylpyrazolo[5,1-c][1,2,4]benzotriazine 5-oxides 8-substituted, ligands at GABAA/benzodiazepine receptor complex: Synthesis, pharmacological and molecular modeling studies
|
Guerrini, Gabriella
|
|
2008
|
16 |
8 |
p. 4471-4489
19 p.
|
artikel
|
| 31 |
Novel azaphilones, kasanosins A and B, which are specific inhibitors of eukaryotic DNA polymerases β and λ from Talaromyces sp.
|
Kimura, Takuma
|
|
2008
|
16 |
8 |
p. 4594-4599
6 p.
|
artikel
|
| 32 |
Novel inhibitors of 17β-hydroxysteroid dehydrogenase type 1: Templates for design
|
Allan, Gillian M.
|
|
2008
|
16 |
8 |
p. 4438-4456
19 p.
|
artikel
|
| 33 |
Potential antitumoral properties of a new copper complex with santonic acid
|
Williams, Patricia A.M.
|
|
2008
|
16 |
8 |
p. 4313-4322
10 p.
|
artikel
|
| 34 |
Proteasome inhibition by peptide-semicarbazones
|
Leban, Johann
|
|
2008
|
16 |
8 |
p. 4579-4588
10 p.
|
artikel
|
| 35 |
Structure–antifungal activity relationship of His-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH2 and analogues
|
Masman, Marcelo F.
|
|
2008
|
16 |
8 |
p. 4347-4358
12 p.
|
artikel
|
| 36 |
Syntheses of 4,6′-epoxymorphinan derivatives and their pharmacologies
|
Nemoto, Toru
|
|
2008
|
16 |
8 |
p. 4304-4312
9 p.
|
artikel
|
| 37 |
Synthesis and antibacterial activity of egonol derivatives
|
Öztürk, Safiye Emirdağ
|
|
2008
|
16 |
8 |
p. 4431-4437
7 p.
|
artikel
|
| 38 |
Synthesis and anti-HIV1 biological activity of novel 5″-ATSAO compounds
|
Tomassi, Cyrille
|
|
2008
|
16 |
8 |
p. 4733-4741
9 p.
|
artikel
|
| 39 |
Synthesis and antioxidant properties of novel N-methyl-1,3,4-thiadiazol-2-amine and 4-methyl-2H-1,2,4-triazole-3(4H)-thione derivatives of benzimidazole class
|
Kuş, Canan
|
|
2008
|
16 |
8 |
p. 4294-4303
10 p.
|
artikel
|
| 40 |
Synthesis and biological activities of 2-oxocycloalkylsulfonamides
|
Li, Xinghai
|
|
2008
|
16 |
8 |
p. 4538-4544
7 p.
|
artikel
|
| 41 |
Synthesis and inhibitory activity of oligosaccharide thiazolines as a class of mechanism-based inhibitors for endo-β-N-acetylglucosaminidases
|
Li, Bing
|
|
2008
|
16 |
8 |
p. 4670-4675
6 p.
|
artikel
|
| 42 |
Synthesis and in vitro anti-leishmanial activity of 1-[5-(5-nitrofuran-2-yl)-1,3,4-thiadiazol-2-yl]- and 1-[5-(5-nitrothiophen-2-yl)-1,3,4-thiadiazol-2-yl]-4-aroylpiperazines
|
Behrouzi-Fardmoghadam, Mina
|
|
2008
|
16 |
8 |
p. 4509-4515
7 p.
|
artikel
|
| 43 |
Synthesis and neuropharmacological characterization of 2-O-substituted apomorphines
|
Sipos, Attila
|
|
2008
|
16 |
8 |
p. 4563-4568
6 p.
|
artikel
|
| 44 |
Synthesis and structure–activity relationship studies on tryprostatin A, an inhibitor of breast cancer resistance protein
|
Jain, Hiteshkumar D.
|
|
2008
|
16 |
8 |
p. 4626-4651
26 p.
|
artikel
|
| 45 |
Synthesis, checkpoint kinase 1 inhibitory properties and in vitro antiproliferative activities of new pyrrolocarbazoles
|
Conchon, Elisabeth
|
|
2008
|
16 |
8 |
p. 4419-4430
12 p.
|
artikel
|
| 46 |
Synthesis, cytotoxic activities and structure–activity relationships of topoisomerase I inhibitors: Indolizinoquinoline-5,12-dione derivatives
|
Cheng, Yu
|
|
2008
|
16 |
8 |
p. 4617-4625
9 p.
|
artikel
|
| 47 |
Synthesis, in vitro pharmacology, and pharmacokinetic profiles of 2-[1-amino-1-carboxy-2-(9H-xanthen-9-yl)-ethyl]-1-fluorocyclopropanecarboxylic acid and its 6-heptyl ester, a potent mGluR2 antagonist
|
Sakagami, Kazunari
|
|
2008
|
16 |
8 |
p. 4359-4366
8 p.
|
artikel
|
| 48 |
Synthesis of caged 2,3,3a,7a-tetrahydro-3,6-methanobenzofuran-7(6H)-ones: Evaluating the minimum structure for apoptosis induction by gambogic acid
|
Kuemmerle, Jared
|
|
2008
|
16 |
8 |
p. 4233-4241
9 p.
|
artikel
|
| 49 |
Synthesis of new N-phenylpyrazole derivatives with potent antimicrobial activity
|
Farag, Ahmad M.
|
|
2008
|
16 |
8 |
p. 4569-4578
10 p.
|
artikel
|
| 50 |
Synthesis of 1-substituted 3-pyridinylmethylidenylindolin-2-ones and 1-substituted 3-quinolinylmethylidenylindolin-2-ones as the enhancers of ATRA-induced differentiation in HL-60 cells
|
Hung, Chi-Ying
|
|
2008
|
16 |
8 |
p. 4222-4232
11 p.
|
artikel
|
| 51 |
Synthesis of 1-/2-substituted-[1,2,3]triazolo[4,5-g]phthalazine-4,9-diones and evaluation of their cytotoxicity and topoisomerase II inhibition
|
Kim, Jin Sung
|
|
2008
|
16 |
8 |
p. 4545-4550
6 p.
|
artikel
|
| 52 |
Synthesis, SAR and in vitro evaluation of new cyclic Arg-Gly-Asp pseudopentapeptides containing a s-cis peptide bond as integrin αvβ3 and αvβ5 ligands
|
Salvati, Maria
|
|
2008
|
16 |
8 |
p. 4262-4271
10 p.
|
artikel
|
| 53 |
Tetramic and tetronic acids: An update on new derivatives and biological aspects
|
Schobert, Rainer
|
|
2008
|
16 |
8 |
p. 4203-4221
19 p.
|
artikel
|
| 54 |
The role of lipophilicity in determining binding affinity and functional activity for 5-HT2A receptor ligands
|
Parker, Matthew A.
|
|
2008
|
16 |
8 |
p. 4661-4669
9 p.
|
artikel
|
| 55 |
The role of methylglyoxal in the non-enzymatic conversion of tryptophan, its methyl ester and tryptamine to 1-acetyl-β-carbolines
|
Nemet, Ina
|
|
2008
|
16 |
8 |
p. 4551-4562
12 p.
|
artikel
|
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