nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Allele-specific inhibition of divergent protein tyrosine phosphatases with a single small molecule
|
Zhang, Xin-Yu |
|
2008 |
16 |
17 |
p. 8090-8097 8 p. |
artikel |
2 |
A new synthetic access to furo[3,2-f]chromene analogues of an antimycobacterial
|
Alvey, Luke |
|
2008 |
16 |
17 |
p. 8264-8272 9 p. |
artikel |
3 |
Antibacterial profile against drug-resistant Staphylococcus epidermidis clinical strain and structure–activity relationship studies of 1H-pyrazolo[3,4-b]pyridine and thieno[2,3-b]pyridine derivatives
|
Leal, Bruno |
|
2008 |
16 |
17 |
p. 8196-8204 9 p. |
artikel |
4 |
Antifungal activity of synthetic di(hetero)arylamines based on the benzo[b]thiophene moiety
|
Pinto, Eugénia |
|
2008 |
16 |
17 |
p. 8172-8177 6 p. |
artikel |
5 |
Anti-HIV-1 activity of phloroglucinol derivative, 6,6′-bieckol, from Ecklonia cava
|
Artan, Murat |
|
2008 |
16 |
17 |
p. 7921-7926 6 p. |
artikel |
6 |
Antiproliferative and apoptosis-inducing activities of alkyl gallate and gallamide derivatives related to (−)-epigallocatechin gallate
|
Dodo, Kosuke |
|
2008 |
16 |
17 |
p. 7975-7982 8 p. |
artikel |
7 |
Characterization of the binding properties of SIRT2 inhibitors with a N-(3-phenylpropenoyl)-glycine tryptamide backbone
|
Kiviranta, Päivi H. |
|
2008 |
16 |
17 |
p. 8054-8062 9 p. |
artikel |
8 |
Chemoenzymatic syntheses of prenylated aromatic small molecules using Streptomyces prenyltransferases with relaxed substrate specificities
|
Kumano, Takuto |
|
2008 |
16 |
17 |
p. 8117-8126 10 p. |
artikel |
9 |
5-(4-Chlorophenyl)-5,6-dihydro-1,3-oxazepin-7(4H)-one derivatives as lipophilic cyclic analogues of baclofen: Design, synthesis, and neuropharmacological evaluation
|
Abdel-Hafez, Atef A. |
|
2008 |
16 |
17 |
p. 7983-7991 9 p. |
artikel |
10 |
Comparative docking studies of labdane-type diterpenes with forskolin at the active site of adenylyl cyclase
|
Koukoulitsa, Catherine |
|
2008 |
16 |
17 |
p. 8237-8243 7 p. |
artikel |
11 |
Computer based design, synthesis and biological evaluation of novel indole derivatives as HCV NS3-4A serine protease inhibitors
|
Ismail, Nasser S.M. |
|
2008 |
16 |
17 |
p. 7877-7887 11 p. |
artikel |
12 |
Cyclic voltammetric analysis of 2-styrylchromones: Relationship with the antioxidant activity
|
Gomes, Ana |
|
2008 |
16 |
17 |
p. 7939-7943 5 p. |
artikel |
13 |
Design and SAR of new substituted purines bearing aryl groups at N9 position as HIV-1 Tat–TAR interaction inhibitors
|
Pang, Ruifang |
|
2008 |
16 |
17 |
p. 8178-8186 9 p. |
artikel |
14 |
Design and synthesis of a metabolically stable and potent antitussive agent, a novel δ opioid receptor antagonist, TRK-851
|
Sakami, Satoshi |
|
2008 |
16 |
17 |
p. 7956-7967 12 p. |
artikel |
15 |
Design and synthesis of carborane-containing androgen receptor (AR) antagonist bearing a pyridine ring
|
Ohta, Kiminori |
|
2008 |
16 |
17 |
p. 8022-8028 7 p. |
artikel |
16 |
Design, synthesis, and acetylcholinesterase inhibitory activity of novel coumarin analogues
|
Zhou, Xiang |
|
2008 |
16 |
17 |
p. 8011-8021 11 p. |
artikel |
17 |
Design, synthesis, and antitumor activity of new bis-aminomethylnaphthalenes
|
Bollini, Mariela |
|
2008 |
16 |
17 |
p. 8003-8010 8 p. |
artikel |
18 |
Design, synthesis and biological evaluation of dihydronaphthalene and benzosuberene analogs of the combretastatins as inhibitors of tubulin polymerization in cancer chemotherapy
|
Sriram, Madhavi |
|
2008 |
16 |
17 |
p. 8161-8171 11 p. |
artikel |
19 |
Design, synthesis and biological evaluation of novel compounds with conjugated structure as anti-tumor agents
|
Su, Hong |
|
2008 |
16 |
17 |
p. 7992-8002 11 p. |
artikel |
20 |
Editorial board
|
|
|
2008 |
16 |
17 |
p. IFC- 1 p. |
artikel |
21 |
Furoxan-, alkylnitrate-derivatives and related compounds as anti-trypanosomatid agents: Mechanism of action studies
|
Boiani, Lucı´a |
|
2008 |
16 |
17 |
p. 7900-7907 8 p. |
artikel |
22 |
Graphical contents list
|
|
|
2008 |
16 |
17 |
p. 7863-7876 14 p. |
artikel |
23 |
Hybridization-dependent fluorescence of oligodeoxynucleotides incorporating new pyrene-modified adenosine residues
|
Seio, Kohji |
|
2008 |
16 |
17 |
p. 8287-8293 7 p. |
artikel |
24 |
Identification of SVM-based classification model, synthesis and evaluation of prenylated flavonoids as vasorelaxant agents
|
Dong, Xiaowu |
|
2008 |
16 |
17 |
p. 8151-8160 10 p. |
artikel |
25 |
Instructions to contributors
|
|
|
2008 |
16 |
17 |
p. I- 1 p. |
artikel |
26 |
In vitro antifungal activity of polyfunctionalized 2-(hetero)arylquinolines prepared through imino Diels–Alder reactions
|
Meléndez Gómez, Carlos M. |
|
2008 |
16 |
17 |
p. 7908-7920 13 p. |
artikel |
27 |
Molecular modeling and dynamics studies of Shikimate Kinase from Bacillus anthracis
|
Pauli, Ivani |
|
2008 |
16 |
17 |
p. 8098-8108 11 p. |
artikel |
28 |
Monoquaternary pyridinium salts with modified side chain—synthesis and evaluation on model of tabun- and paraoxon-inhibited acetylcholinesterase
|
Musilek, Kamil |
|
2008 |
16 |
17 |
p. 8218-8223 6 p. |
artikel |
29 |
New QSPR study for the prediction of aqueous solubility of drug-like compounds
|
Duchowicz, Pablo R. |
|
2008 |
16 |
17 |
p. 7944-7955 12 p. |
artikel |
30 |
NO-donors. Part 17 1 : Synthesis and antimicrobial activity of novel ketoconazole–NO-donor hybrid compounds
|
Konter, Joerg |
|
2008 |
16 |
17 |
p. 8294-8300 7 p. |
artikel |
31 |
Novel azolyl-(phenylmethyl)]aryl/heteroarylamines: Potent CYP26 inhibitors and enhancers of all-trans retinoic acid activity in neuroblastoma cells
|
Gomaa, Mohamed Sayed |
|
2008 |
16 |
17 |
p. 8301-8313 13 p. |
artikel |
32 |
Novel synthesis and pharmacological evaluation as α2-adrenoceptor ligands of O-phenylisouronium salts
|
Goonan, Áine |
|
2008 |
16 |
17 |
p. 8210-8217 8 p. |
artikel |
33 |
N-Propynyl analogs of β-phenylethylidenehydrazines: Synthesis and evaluation of effects on glycine, GABA, and monoamine oxidase
|
MacKenzie, Erin M. |
|
2008 |
16 |
17 |
p. 8254-8263 10 p. |
artikel |
34 |
Pestalachlorides A–C, antifungal metabolites from the plant endophytic fungus Pestalotiopsis adusta
|
Li, Erwei |
|
2008 |
16 |
17 |
p. 7894-7899 6 p. |
artikel |
35 |
Potent CCR4 antagonists: Synthesis, evaluation, and docking study of 2,4-diaminoquinazolines
|
Yokoyama, Kazuhiro |
|
2008 |
16 |
17 |
p. 7968-7974 7 p. |
artikel |
36 |
Quantitative structure–activity relationship studies on nitrofuranyl anti-tubercular agents
|
Hevener, Kirk E. |
|
2008 |
16 |
17 |
p. 8042-8053 12 p. |
artikel |
37 |
Spin trapping experiments with different carbamoyl-substituted EMPO derivatives
|
Stolze, Klaus |
|
2008 |
16 |
17 |
p. 8082-8089 8 p. |
artikel |
38 |
Stress-driven discovery of metabolites from the phytopathogenic fungus Leptosphaeria maculans: Structure and activity of leptomaculins A–E
|
Pedras, M. Soledade C. |
|
2008 |
16 |
17 |
p. 8063-8071 9 p. |
artikel |
39 |
Structure–activity relationships of new inhibitors of breast cancer resistance protein (ABCG2)
|
Pick, Anne |
|
2008 |
16 |
17 |
p. 8224-8236 13 p. |
artikel |
40 |
Syntheses and anti-depressant activity of 5-amino-1, 3, 4-thiadiazole-2-thiol imines and thiobenzyl derivatives
|
Yusuf, Mohammad |
|
2008 |
16 |
17 |
p. 8029-8034 6 p. |
artikel |
41 |
Synthesis and antimicrobial activity of dermaseptin S1 analogues
|
Savoia, Dianella |
|
2008 |
16 |
17 |
p. 8205-8209 5 p. |
artikel |
42 |
Synthesis and antiproliferative activity in vitro of novel (2-butynyl)thioquinolines
|
Mól, W. |
|
2008 |
16 |
17 |
p. 8136-8141 6 p. |
artikel |
43 |
Synthesis and bio-evaluation of a new fatty acid derivative for myocardial imaging
|
Mathur, Anupam |
|
2008 |
16 |
17 |
p. 7927-7931 5 p. |
artikel |
44 |
Synthesis and biological evaluation of glucuronide prodrugs of the histone deacetylase inhibitor CI-994 for application in selective cancer chemotherapy
|
Thomas, Mickaël |
|
2008 |
16 |
17 |
p. 8109-8116 8 p. |
artikel |
45 |
Synthesis and elastase-inhibiting activity of 2-pyridinyl-isothiazol-3(2H)-one 1,1-dioxides
|
Eilfeld, Alexander |
|
2008 |
16 |
17 |
p. 8127-8135 9 p. |
artikel |
46 |
Synthesis and evaluation of curcumin analogues as potential thioredoxin reductase inhibitors
|
Qiu, Xu |
|
2008 |
16 |
17 |
p. 8035-8041 7 p. |
artikel |
47 |
Synthesis and structure–activity relationship studies of theophylline analogs on population responses in the rat hippocampus in vitro
|
Ananthalakshmi, Kethireddy V.V. |
|
2008 |
16 |
17 |
p. 8142-8150 9 p. |
artikel |
48 |
Synthesis, in vitro, and in vivo biological evaluation and molecular docking simulations of chiral alcohol and ether derivatives of the 1,5-diarylpyrrole scaffold as novel anti-inflammatory and analgesic agents
|
Biava, Mariangela |
|
2008 |
16 |
17 |
p. 8072-8081 10 p. |
artikel |
49 |
Synthesis of both enantiomers of hydroxypipecolic acid derivatives equivalent to 5-azapyranuronic acids and evaluation of their inhibitory activities against glycosidases
|
Yoshimura, Yuichi |
|
2008 |
16 |
17 |
p. 8273-8286 14 p. |
artikel |
50 |
Synthesis of new sulfonyl pyrrolidine derivatives as matrix metalloproteinase inhibitors
|
Cheng, Xian-Chao |
|
2008 |
16 |
17 |
p. 7932-7938 7 p. |
artikel |
51 |
Synthesis, structural studies and biological properties of new TBA analogues containing an acyclic nucleotide
|
Coppola, Teresa |
|
2008 |
16 |
17 |
p. 8244-8253 10 p. |
artikel |
52 |
The efficacy and selectivity of tumor cell killing by Akt inhibitors are substantially increased by chloroquine
|
Hu, Changkun |
|
2008 |
16 |
17 |
p. 7888-7893 6 p. |
artikel |
53 |
Thiazolidinone CFTR inhibitors with improved water solubility identified by structure–activity analysis
|
Sonawane, N.D. |
|
2008 |
16 |
17 |
p. 8187-8195 9 p. |
artikel |