nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A class of novel carboline intercalators: Their synthesis, in vitro anti-proliferation, in vivo anti-tumor action, and 3D QSAR analysis
|
Wu, Jianhui |
|
2010 |
18 |
17 |
p. 6220-6229 10 p. |
artikel |
2 |
6-Alkylquinolone-3-carboxylic acid tethered to macrolides synthesis and antimicrobial profile
|
Kapić, Samra |
|
2010 |
18 |
17 |
p. 6569-6577 9 p. |
artikel |
3 |
Antiviral agents 2. Synthesis of trimeric naphthoquinone analogues of conocurvone and their antiviral evaluation against HIV
|
Crosby, Ian T. |
|
2010 |
18 |
17 |
p. 6442-6450 9 p. |
artikel |
4 |
Conjugates of betulin derivatives with AZT as potent anti-HIV agents
|
Xiong, Juan |
|
2010 |
18 |
17 |
p. 6451-6469 19 p. |
artikel |
5 |
Design, synthesis and anticholinesterase activity of a novel series of 1-benzyl-4-((6-alkoxy-3-oxobenzofuran-2(3H)-ylidene) methyl) pyridinium derivatives
|
Nadri, Hamid |
|
2010 |
18 |
17 |
p. 6360-6366 7 p. |
artikel |
6 |
Design, synthesis, and biological evaluation of conformationally constrained glycerol 3-phosphate acyltransferase inhibitors
|
Wydysh, Edward A. |
|
2010 |
18 |
17 |
p. 6470-6479 10 p. |
artikel |
7 |
Design, synthesis, and cholesterol-lowering efficacy for prodrugs of berberrubine
|
Li, Ying-Hong |
|
2010 |
18 |
17 |
p. 6422-6428 7 p. |
artikel |
8 |
Design, synthesis, and evaluation of quinazoline T cell proliferation inhibitors
|
Sagiv-Barfi, Idit |
|
2010 |
18 |
17 |
p. 6404-6413 10 p. |
artikel |
9 |
Design, synthesis, and in vitro antiprotozoal, antimycobacterial activities of N-{2-[(7-chloroquinolin-4-yl)amino]ethyl}ureas
|
Nava-Zuazo, Carlos |
|
2010 |
18 |
17 |
p. 6398-6403 6 p. |
artikel |
10 |
Design, synthesis, and pharmacological effects of structurally simple ligands for MT1 and MT2 melatonin receptors
|
Carocci, Alessia |
|
2010 |
18 |
17 |
p. 6496-6511 16 p. |
artikel |
11 |
Discovery of achiral inhibitors of the hepatitis C virus NS3 protease based on 2(1H)-pyrazinones
|
Örtqvist, Pernilla |
|
2010 |
18 |
17 |
p. 6512-6525 14 p. |
artikel |
12 |
Discovery of 2-(4-((1H-1,2,4-triazol-1-yl)methyl)-5-(4-bromophenyl)-1-(2-chlorophenyl)-1H-pyrazol-3-yl)-5-tert-butyl-1,3,4-thiadiazole (GCC2680) as a potent, selective and orally efficacious cannabinoid-1 receptor antagonist
|
Lee, Jinhwa |
|
2010 |
18 |
17 |
p. 6377-6388 12 p. |
artikel |
13 |
Editorial board
|
|
|
2010 |
18 |
17 |
p. IFC- 1 p. |
artikel |
14 |
Facile synthesis of peptide–porphyrin conjugates: Towards artificial catalase
|
Umezawa, Naoki |
|
2010 |
18 |
17 |
p. 6340-6350 11 p. |
artikel |
15 |
Glycopeptide dendrimer colchicine conjugates targeting cancer cells
|
Johansson, Emma M.V. |
|
2010 |
18 |
17 |
p. 6589-6597 9 p. |
artikel |
16 |
Graphical contents list
|
|
|
2010 |
18 |
17 |
p. 6209-6219 11 p. |
artikel |
17 |
Iodination of verapamil for a stronger induction of death, through GSH efflux, of cancer cells overexpressing MRP1
|
Barattin, Régis |
|
2010 |
18 |
17 |
p. 6265-6274 10 p. |
artikel |
18 |
Modulation of the inhibitor properties of dipeptidyl (acyloxy)methyl ketones toward the CaaX proteases
|
Dechert, Anne-Marie R. |
|
2010 |
18 |
17 |
p. 6230-6237 8 p. |
artikel |
19 |
New antitumoral agents I: In vitro anticancer activity and in vivo acute toxicity of synthetic 1,5-bis(4-hydroxy-3-methoxyphenyl)-1,4-pentadien-3-one and derivatives
|
Quincoces Suarez, José Agustín |
|
2010 |
18 |
17 |
p. 6275-6281 7 p. |
artikel |
20 |
New effective inhibitors of the Abelson kinase
|
Kraus, George A. |
|
2010 |
18 |
17 |
p. 6316-6321 6 p. |
artikel |
21 |
New 4H-chromen-4-one and 2H-chromene derivatives as anti-picornavirus capsid-binders
|
Conti, Cinzia |
|
2010 |
18 |
17 |
p. 6480-6488 9 p. |
artikel |
22 |
New synthetic flavone derivatives induce apoptosis of hepatocarcinoma cells
|
Liu, Huachen |
|
2010 |
18 |
17 |
p. 6322-6328 7 p. |
artikel |
23 |
N G-Acyl-argininamides as NPY Y1 receptor antagonists: Influence of structurally diverse acyl substituents on stability and affinity
|
Weiss, Stefan |
|
2010 |
18 |
17 |
p. 6292-6304 13 p. |
artikel |
24 |
Novel nucleosides as potent influenza viral inhibitors
|
Vedula, Manohar Sharma |
|
2010 |
18 |
17 |
p. 6329-6339 11 p. |
artikel |
25 |
4″-O-(ω-Quinolylamino-alkylamino)propionyl derivatives of selected macrolides with the activity against the key erythromycin resistant respiratory pathogens
|
Fajdetić, A. |
|
2010 |
18 |
17 |
p. 6559-6568 10 p. |
artikel |
26 |
Potential anti-inflammatory phenolic glycosides from the medicinal plant Moringa oleifera fruits
|
Cheenpracha, Sarot |
|
2010 |
18 |
17 |
p. 6598-6602 5 p. |
artikel |
27 |
Radiosynthesis and in vivo evaluation of [11C]MC80 for P-glycoprotein imaging
|
Bruyne, Sylvie De |
|
2010 |
18 |
17 |
p. 6489-6495 7 p. |
artikel |
28 |
Selective inhibition of methoxyflavonoids on human CYP1B1 activity
|
Takemura, Hitomi |
|
2010 |
18 |
17 |
p. 6310-6315 6 p. |
artikel |
29 |
Structure-based design, synthesis, and biological evaluation of lipophilic-tailed monocationic inhibitors of neuronal nitric oxide synthase
|
Xue, Fengtian |
|
2010 |
18 |
17 |
p. 6526-6537 12 p. |
artikel |
30 |
Studies on preparation and photodynamic mechanism of chlorin P6-13,15-N-(cyclohexyl)cycloimide (Chlorin-H) and its antitumor effect for photodynamic therapy in vitro and in vivo
|
Yan, Yi-jia |
|
2010 |
18 |
17 |
p. 6282-6291 10 p. |
artikel |
31 |
Synthesis, activity, and pharmacokinetic properties of a series of conformationally-restricted thiourea analogs as novel hepatitis C virus inhibitors
|
Kang, Iou-Jiun |
|
2010 |
18 |
17 |
p. 6414-6421 8 p. |
artikel |
32 |
Synthesis and biological activity of 4″-O-acyl derivatives of 14- and 15-membered macrolides linked to ω-quinolone-carboxylic unit
|
Škugor, Maja Matanović |
|
2010 |
18 |
17 |
p. 6547-6558 12 p. |
artikel |
33 |
Synthesis and biological evaluation of vitamin K derivatives as angiogenesis inhibitor
|
Kayashima, Tomoko |
|
2010 |
18 |
17 |
p. 6305-6309 5 p. |
artikel |
34 |
Synthesis and characterization of mitoQ and idebenone analogues as mediators of oxygen consumption in mitochondria
|
Duveau, Damien Y. |
|
2010 |
18 |
17 |
p. 6429-6441 13 p. |
artikel |
35 |
Synthesis and in vitro antitumor activity of new 4,5-dihydropyrazole derivatives
|
Congiu, Cenzo |
|
2010 |
18 |
17 |
p. 6238-6248 11 p. |
artikel |
36 |
Synthesis and properties of macrolones characterized by two ether bonds in the linker
|
Jakopović, Ivana Palej |
|
2010 |
18 |
17 |
p. 6578-6588 11 p. |
artikel |
37 |
Synthesis and properties of triplex-forming oligonucleotides containing 2′-O-(2-methoxyethyl)-5-(3-aminoprop-1-ynyl)-uridine
|
Lou, Chenguang |
|
2010 |
18 |
17 |
p. 6389-6397 9 p. |
artikel |
38 |
Synthesis and ribonuclease A inhibition activity of resorcinol and phloroglucinol derivatives of catechin and epicatechin: Importance of hydroxyl groups
|
Dutta, Sansa |
|
2010 |
18 |
17 |
p. 6538-6546 9 p. |
artikel |
39 |
Synthesis, biological evaluation, and docking studies of novel heterocyclic diaryl compounds as selective COX-2 inhibitors
|
Eren, Gökçen |
|
2010 |
18 |
17 |
p. 6367-6376 10 p. |
artikel |
40 |
Synthesis, biological evaluation, and structure–activity relationship study of novel cytotoxic aza-caffeic acid derivatives
|
Zou, Hongbin |
|
2010 |
18 |
17 |
p. 6351-6359 9 p. |
artikel |
41 |
The unsaturated acyclic nucleoside analogues bearing a sterically constrained (Z)-4′-benzamido-2′-butenyl moiety: Synthesis, X-ray crystal structure study, cytostatic and antiviral activity evaluations
|
Benci, Krešimir |
|
2010 |
18 |
17 |
p. 6249-6257 9 p. |
artikel |
42 |
Xanthones with neuraminidase inhibitory activity from the seedcases of Garcinia mangostana
|
Ryu, Hyung Won |
|
2010 |
18 |
17 |
p. 6258-6264 7 p. |
artikel |