nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A CoMSIA study on the adenosine kinase inhibition of pyrrolo[2,3-d]pyrimidine nucleoside analogues
|
Caballero, Julio |
|
2008 |
16 |
9 |
p. 5103-5108 6 p. |
artikel |
2 |
Active core structure of terfestatin A, a new specific inhibitor of auxin signaling
|
Hayashi, Ken-ichiro |
|
2008 |
16 |
9 |
p. 5331-5344 14 p. |
artikel |
3 |
Additive SMILES-based optimal descriptors in QSAR modelling bee toxicity: Using rare SMILES attributes to define the applicability domain
|
Toropov, A.A. |
|
2008 |
16 |
9 |
p. 4801-4809 9 p. |
artikel |
4 |
An epoxidation mechanism of carbamazepine by CYP3A4
|
Hata, Masayuki |
|
2008 |
16 |
9 |
p. 5134-5148 15 p. |
artikel |
5 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2008 |
16 |
9 |
p. 5352-5354 3 p. |
artikel |
6 |
Carboxymethylated pyridoindole antioxidants as aldose reductase inhibitors: Synthesis, activity, partitioning, and molecular modeling
|
Stefek, Milan |
|
2008 |
16 |
9 |
p. 4908-4920 13 p. |
artikel |
7 |
Characterization of chemical components in extracts from Si-wu decoction with proliferation-promoting effects on rat mesenchymal stem cells
|
Zeng, He-Ping |
|
2008 |
16 |
9 |
p. 5109-5114 6 p. |
artikel |
8 |
Characterization, phase-solubility, and molecular modeling of inclusion complex of 5-nitroindazole derivative with cyclodextrins
|
Jullian, Carolina |
|
2008 |
16 |
9 |
p. 5078-5084 7 p. |
artikel |
9 |
Chemical and biological investigation of N-hydroxy-valdecoxib: An active metabolite of valdecoxib
|
Erdélyi, Péter |
|
2008 |
16 |
9 |
p. 5322-5330 9 p. |
artikel |
10 |
Chemical synthesis of 2β-amino-5α-androstane-3α,17β-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells
|
Thibeault, Dominic |
|
2008 |
16 |
9 |
p. 5062-5077 16 p. |
artikel |
11 |
Chemoenzymatic synthesis of polyprenyl phosphates
|
Hartley, Meredith D. |
|
2008 |
16 |
9 |
p. 5149-5156 8 p. |
artikel |
12 |
Design and synthesis of benzofuranic derivatives as new ligands at the melatonin-binding site MT 3
|
Ettaoussi, Mohamed |
|
2008 |
16 |
9 |
p. 4954-4962 9 p. |
artikel |
13 |
Design, synthesis, and anticonvulsant activity of N-phenylamino derivatives of 3,3-dialkyl-pyrrolidine-2,5-diones and hexahydro-isoindole-1,3-diones
|
Kamiński, Krzysztof |
|
2008 |
16 |
9 |
p. 4921-4931 11 p. |
artikel |
14 |
Design, synthesis, and biological evaluation of glycine-based molecular tongs as inhibitors of Aβ1–40 aggregation in vitro
|
Cellamare, Saverio |
|
2008 |
16 |
9 |
p. 4810-4822 13 p. |
artikel |
15 |
Design, synthesis and trypanocidal activity of lead compounds based on inhibitors of parasite glycolysis
|
Nowicki, Matthew W. |
|
2008 |
16 |
9 |
p. 5050-5061 12 p. |
artikel |
16 |
1,5-Disubstituted 1,2,3-triazoles as cis-restricted analogues of combretastatin A-4: Synthesis, molecular modeling and evaluation as cytotoxic agents and inhibitors of tubulin
|
Odlo, Kristin |
|
2008 |
16 |
9 |
p. 4829-4838 10 p. |
artikel |
17 |
Editorial board
|
|
|
2008 |
16 |
9 |
p. IFC- 1 p. |
artikel |
18 |
Effect of novel N-aryl sulfonamide substituted 3-morpholino arecoline derivatives as muscarinic receptor 1 agonists in Alzheimer’s dementia models
|
Kumar, Y.C. Sunil |
|
2008 |
16 |
9 |
p. 5157-5163 7 p. |
artikel |
19 |
Effects of modifications of the linker in a series of phenylpropanoic acid derivatives: Synthesis, evaluation as PPARα/γ dual agonists, and X-ray crystallographic studies
|
Casimiro-Garcia, Agustin |
|
2008 |
16 |
9 |
p. 4883-4907 25 p. |
artikel |
20 |
Efficient synthesis of functionalized oligodeoxyribonucleotides with base-labile groups using a new silyl linker
|
Ohkubo, Akihiro |
|
2008 |
16 |
9 |
p. 5345-5351 7 p. |
artikel |
21 |
Electronically stabilized versions of the antimalarial acetal trioxanes artemether and artesunate
|
Posner, Gary H. |
|
2008 |
16 |
9 |
p. 5247-5253 7 p. |
artikel |
22 |
Facile synthesis of novel mutual derivatives of nucleosides and pyrimidines by regioselectively chemo-enzymatic protocol
|
Qian, Xueqi |
|
2008 |
16 |
9 |
p. 5181-5188 8 p. |
artikel |
23 |
Graphical contents list
|
|
|
2008 |
16 |
9 |
p. 4745-4758 14 p. |
artikel |
24 |
Hymenoic acid, a novel specific inhibitor of human DNA polymerase λ from a fungus of Hymenochaetaceae sp.
|
Nishida, Masayuki |
|
2008 |
16 |
9 |
p. 5115-5122 8 p. |
artikel |
25 |
Instructions to contributors
|
|
|
2008 |
16 |
9 |
p. I- 1 p. |
artikel |
26 |
Interaction between artemisinin and heme. A Density Functional Theory study of structures and interaction energies
|
Araújo, Jocley Queiroz |
|
2008 |
16 |
9 |
p. 5021-5029 9 p. |
artikel |
27 |
Isocoumarin-based inhibitors of pancreatic cholesterol esterase
|
Heynekamp, Justin J. |
|
2008 |
16 |
9 |
p. 5285-5294 10 p. |
artikel |
28 |
Microbial metabolism of 1-aminoanthracene by Beauveria bassiana
|
Zhan, Jixun |
|
2008 |
16 |
9 |
p. 5085-5089 5 p. |
artikel |
29 |
Modifying the N-terminus of polyamides: PyImPyIm has improved sequence specificity over f-ImPyIm
|
Brown, Toni |
|
2008 |
16 |
9 |
p. 5266-5276 11 p. |
artikel |
30 |
Molecular modeling and dynamics simulations of PNP from Streptococcus agalactiae
|
Caceres, Rafael Andrade |
|
2008 |
16 |
9 |
p. 4984-4993 10 p. |
artikel |
31 |
No carrier added synthesis of O-(2′-[18F]fluoroethyl)-l-tyrosine via a novel type of chiral enantiomerically pure precursor, NiII complex of a (S)-tyrosine Schiff base
|
Krasikova, Raisa N. |
|
2008 |
16 |
9 |
p. 4994-5003 10 p. |
artikel |
32 |
Novel antioxidant agents deriving from molecular combination of Vitamin C and NO-donor moieties
|
Cena, Clara |
|
2008 |
16 |
9 |
p. 5199-5206 8 p. |
artikel |
33 |
Novel 5-azaindolocarbazoles as cytotoxic agents and Chk1 inhibitors
|
Lefoix, Myriam |
|
2008 |
16 |
9 |
p. 5303-5321 19 p. |
artikel |
34 |
Novel thiosemicarbazone derivatives as potential antitumor agents: Synthesis, physicochemical and structural properties, DNA interactions and antiproliferative activity
|
Đilović, Ivica |
|
2008 |
16 |
9 |
p. 5189-5198 10 p. |
artikel |
35 |
Rational design, synthesis, and in vivo evaluation of the antileukemic activity of six new alkylating steroidal esters
|
Koutsourea, Anna I. |
|
2008 |
16 |
9 |
p. 5207-5215 9 p. |
artikel |
36 |
Rationally designed PKA inhibitors for positron emission tomography: Synthesis and cerebral biodistribution of N-(2-(4-bromocinnamylamino)ethyl)-N-[11C]methyl-isoquinoline-5-sulfonamide
|
Vasdev, Neil |
|
2008 |
16 |
9 |
p. 5277-5284 8 p. |
artikel |
37 |
Reaction of 2′-deoxycytidine with peroxynitrite in the presence of ammonium bromide
|
Suzuki, Toshinori |
|
2008 |
16 |
9 |
p. 5164-5170 7 p. |
artikel |
38 |
Recent advances in selective α1-adrenoreceptor antagonists as antihypertensive agents
|
Jain, Kishor S. |
|
2008 |
16 |
9 |
p. 4759-4800 42 p. |
artikel |
39 |
S-Ribosylhomocysteine analogues with the carbon-5 and sulfur atoms replaced by a vinyl or (fluoro)vinyl unit
|
Wnuk, Stanislaw F. |
|
2008 |
16 |
9 |
p. 5090-5102 13 p. |
artikel |
40 |
Structural insights into the Plasmodium falciparum histone deacetylase 1 (PfHDAC-1): A novel target for the development of antimalarial therapy
|
Mukherjee, Prasenjit |
|
2008 |
16 |
9 |
p. 5254-5265 12 p. |
artikel |
41 |
Structure–activity relationship of truncated analogs of caprazamycins as potential anti-tuberculosis agents
|
Hirano, Shinpei |
|
2008 |
16 |
9 |
p. 5123-5133 11 p. |
artikel |
42 |
Structure-based discovery of a novel non-peptidic small molecular inhibitor of caspase-3
|
Sakai, Junichi |
|
2008 |
16 |
9 |
p. 4854-4859 6 p. |
artikel |
43 |
Syntheses and applications of fluorescent and biotinylated epolactaene derivatives: Epolactaene and its derivative induce disulfide formation
|
Kuramochi, Kouji |
|
2008 |
16 |
9 |
p. 5039-5049 11 p. |
artikel |
44 |
Synthesis and anti-Trypanosoma cruzi activity of derivatives from nor-lapachones and lapachones
|
da Silva Júnior, Eufrânio N. |
|
2008 |
16 |
9 |
p. 5030-5038 9 p. |
artikel |
45 |
Synthesis and biological evaluation of thiobenzanilides as anticancer agents
|
Hu, Wan-Ping |
|
2008 |
16 |
9 |
p. 5295-5302 8 p. |
artikel |
46 |
Synthesis and cytotoxic activity of γ-aryl substituted α-alkylidene-γ-lactones and α-alkylidene-γ-lactams
|
Albrecht, Anna |
|
2008 |
16 |
9 |
p. 4872-4882 11 p. |
artikel |
47 |
Synthesis and cytotoxic properties of new fluorodeoxyglucose-coupled chlorambucil derivatives
|
Reux, Bastien |
|
2008 |
16 |
9 |
p. 5004-5020 17 p. |
artikel |
48 |
Synthesis and discovery of a novel pyrazole derivative as an inhibitor of apoptosis through modulating integrin β4, ROS, and p53 levels in vascular endothelial cells
|
Zhao, Bao-Xiang |
|
2008 |
16 |
9 |
p. 5171-5180 10 p. |
artikel |
49 |
Synthesis and structure–activity relationship of histone deacetylase (HDAC) inhibitors with triazole-linked cap group
|
Chen, Po C. |
|
2008 |
16 |
9 |
p. 4839-4853 15 p. |
artikel |
50 |
Synthesis, cytotoxic activity, and SAR analysis of the derivatives of taxchinin A and brevifoliol
|
Zhao, Yu |
|
2008 |
16 |
9 |
p. 4860-4871 12 p. |
artikel |
51 |
Synthesis of 3,5-bis(2-indolyl)pyridine and 3-[(2-indolyl)-5-phenyl]pyridine derivatives as CDK inhibitors and cytotoxic agents
|
Jacquemard, Ulrich |
|
2008 |
16 |
9 |
p. 4932-4953 22 p. |
artikel |
52 |
Synthesis of glutamic acid analogs as potent inhibitors of leukotriene A4 hydrolase
|
Kirkland, Thomas A. |
|
2008 |
16 |
9 |
p. 4963-4983 21 p. |
artikel |
53 |
Thioxophosphoranyl aryl- and heteroaryloxiranes as the representants of a new class of metallocarboxypeptidase inhibitors
|
Fernández, Daniel |
|
2008 |
16 |
9 |
p. 4823-4828 6 p. |
artikel |
54 |
Total syntheses of (±)-ovalicin, C4(S ∗)-isomer, and its C5-analogs and anti-trypanosomal activities
|
Hua, Duy H. |
|
2008 |
16 |
9 |
p. 5232-5246 15 p. |
artikel |
55 |
Trivalent, Gal/GalNAc-containing ligands designed for the asialoglycoprotein receptor
|
Khorev, Oleg |
|
2008 |
16 |
9 |
p. 5216-5231 16 p. |
artikel |