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                             56 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Achiral oligoamines as versatile tool for the development of aspartic protease inhibitors Blum, Andreas
 2008
 16 18 p. 8574-8586
13 p.
 artikel
2 Antimicrobial and cytotoxic arylazoenamines. Part III: Antiviral activity of selected classes of arylazoenamines Tonelli, Michele
 2008
 16 18 p. 8447-8465
19 p.
 artikel
3 Bioorganic & Medicinal Chemistry Reviews and Perspectives 2008
 16 18 p. 8767-8769
3 p.
 artikel
4 Carbonic anhydrase activators: Kinetic and X-ray crystallographic study for the interaction of d- and l-tryptophan with the mammalian isoforms I–XIV Temperini, Claudia
 2008
 16 18 p. 8373-8378
6 p.
 artikel
5 Chemoenzymatic synthesis of N-linked neoglycoproteins through a chitinase-catalyzed transglycosylation Li, Cishan
 2008
 16 18 p. 8366-8372
7 p.
 artikel
6 Conjugates of the fungal cytotoxin illudin M with improved tumour specificity Schobert, Rainer
 2008
 16 18 p. 8592-8597
6 p.
 artikel
7 Corrigendum to “1-, 3- and 8-substituted-9-deazaxanthines as potent and selective antagonists at the human A2B adenosine receptor” [Bioorg. Med. Chem. 16 (2008) 2852–2869] Stefanachi, Angela
 2008
 16 18 p. 8766-
1 p.
 artikel
8 Cyclic diarylheptanoids from Myrica nana inhibiting nitric oxide release Wang, Junfeng
 2008
 16 18 p. 8510-8515
6 p.
 artikel
9 CYP19 (aromatase): Exploring the scaffold flexibility for novel selective inhibitors Castellano, Sabrina
 2008
 16 18 p. 8349-8358
10 p.
 artikel
10 Derivatives of 1,4-bis(3-hydroxycarbonyl-4-hydroxyl)styrylbenzene as PTP1B inhibitors with hypoglycemic activity Shrestha, Suja
 2008
 16 18 p. 8643-8652
10 p.
 artikel
11 Design and synthesis of 6-fluoro-2-naphthyl derivatives as novel CCR3 antagonists with reduced CYP2D6 inhibition Sato, Ippei
 2008
 16 18 p. 8607-8618
12 p.
 artikel
12 Design, synthesis, and biological evaluation of new mitonafide derivatives as potential antitumor drugs Antonini, Ippolito
 2008
 16 18 p. 8440-8446
7 p.
 artikel
13 Development and biological evaluation of C60 fulleropyrrolidine-thalidomide dyad as a new anti-inflammation agent Huang, Sheng-Tung
 2008
 16 18 p. 8619-8626
8 p.
 artikel
14 Dihydropyridines and atypical MDR: A novel perspective of designing general reversal agents for both typical and atypical MDR Miri, Ramin
 2008
 16 18 p. 8329-8334
6 p.
 artikel
15 Dual inhibition of monoamine oxidase B and antagonism of the adenosine A2A receptor by (E,E)-8-(4-phenylbutadien-1-yl)caffeine analogues Pretorius, Judey
 2008
 16 18 p. 8676-8684
9 p.
 artikel
16 Editorial board 2008
 16 18 p. IFC-
1 p.
 artikel
17 Erratum to “Selective angiotensin II AT2 receptor agonists: Benzamide structure–activity relationships” [Bioorg. Med. Chem. 16 (2008) 6841–6849] Wallinder, Charlotta
 2008
 16 18 p. 8765-
1 p.
 artikel
18 Graphical contents list 2008
 16 18 p. 8315-8328
14 p.
 artikel
19 Improvement of water solubility of non-competitive AMPA receptor antagonists by complexation with β-cyclodextrin Stancanelli, Rosanna
 2008
 16 18 p. 8706-8712
7 p.
 artikel
20 Instructions to contributors 2008
 16 18 p. I-
1 p.
 artikel
21 Introduction of the 4-(4-bromophenyl)benzenesulfonyl group to hydrazide analogs of Ilomastat leads to potent gelatinase B (MMP-9) inhibitors with improved selectivity LeDour, Gwennaël
 2008
 16 18 p. 8745-8759
15 p.
 artikel
22 Molecular modeling studies toward the structural optimization of new cyclopeptide-based HDAC inhibitors modeled on the natural product FR235222 Di Micco, Simone
 2008
 16 18 p. 8635-8642
8 p.
 artikel
23 New lithocholic and chenodeoxycholic piperazinylcarboxamides with antiproliferative and pro-apoptotic effects on human cancer cell lines El Kihel, Laïla
 2008
 16 18 p. 8737-8744
8 p.
 artikel
24 Novel angular furoquinolinones bearing flexible chain as antitumor agent: Design, synthesis, cytotoxic evaluation, and DNA-binding studies Xie, Lijuan
 2008
 16 18 p. 8713-8718
6 p.
 artikel
25 Novel anticancer agents, kayeassamins C−I from the flower of Kayea assamica of Myanmar Win, Nwet Nwet
 2008
 16 18 p. 8653-8660
8 p.
 artikel
26 Novel iron complexes bearing N6-substituted adenosine derivatives: Synthesis, magnetic, 57Fe Mössbauer, DFT, and in vitro cytotoxicity studies Trávníček, Zdeněk
 2008
 16 18 p. 8719-8728
10 p.
 artikel
27 N-Propylnoraporphin-11-O-yl carboxylic esters as potent dopamine D2 and serotonin 5-HT1A receptor dual ligands Liu, Zhili
 2008
 16 18 p. 8335-8338
4 p.
 artikel
28 Nucleosides and oligonucleotides containing 1,2,3-triazole residues with nucleobase tethers: Synthesis via the azide-alkyne ‘click’ reaction Chittepu, Padmaja
 2008
 16 18 p. 8427-8439
13 p.
 artikel
29 Obovatol inhibits colorectal cancer growth by inhibiting tumor cell proliferation and inducing apoptosis Lee, Su-Kyung
 2008
 16 18 p. 8397-8402
6 p.
 artikel
30 Oleanolic acid and its derivatives: New inhibitor of protein tyrosine phosphatase 1B with cellular activities Zhang, Yi-Nan
 2008
 16 18 p. 8697-8705
9 p.
 artikel
31 Piperidine variations in search for non-imidazole histamine H3 receptor ligands Łażewska, Dorota
 2008
 16 18 p. 8729-8736
8 p.
 artikel
32 Preparation and biological evaluation of 5-substituted retinoic acids Wada, Akimori
 2008
 16 18 p. 8471-8481
11 p.
 artikel
33 Salicylanilides: Selective inhibitors of interleukin-12p40 production Brown, Michael E.
 2008
 16 18 p. 8760-8764
5 p.
 artikel
34 Screening of herbal constituents for aromatase inhibitory activity Paoletta, S.
 2008
 16 18 p. 8466-8470
5 p.
 artikel
35 Selective A3 adenosine receptor antagonists derived from nucleosides containing a bicyclo[3.1.0]hexane ring system Melman, Artem
 2008
 16 18 p. 8546-8556
11 p.
 artikel
36 Specific binding capacity of β-cyclodextrin with cis and trans enalapril: Physicochemical characterization and structural studies by molecular modeling Zoppi, Ariana
 2008
 16 18 p. 8403-8412
10 p.
 artikel
37 11-Substituted 2,3-dimethoxy-8,9-methylenedioxybenzo[i]phenanthridine derivatives as novel topoisomerase I-targeting agents Feng, Wei
 2008
 16 18 p. 8598-8606
9 p.
 artikel
38 Suppression of cytokine production in lipopolysaccharide-stimulated mouse macrophages by novel cationic glucosamine derivative involves down-regulation of NF-κB and MAPK expressions Mendis, Eresha
 2008
 16 18 p. 8390-8396
7 p.
 artikel
39 Synthesis and antitumor activity of C-9 epimers of the tetrahydrofuran containing acetogenin 4-deoxyannoreticuin Wang, Feng
 2008
 16 18 p. 8413-8418
6 p.
 artikel
40 Synthesis and antiviral evaluation of acyclic azanucleosides developed from sulfanilamide as a lead structure Gawin, Rafał
 2008
 16 18 p. 8379-8389
11 p.
 artikel
41 Synthesis and biological activity of 1-methyl-tryptophan-tirapazamine hybrids as hypoxia-targeting indoleamine 2,3-dioxygenase inhibitors Nakashima, Hitomi
 2008
 16 18 p. 8661-8669
9 p.
 artikel
42 Synthesis and biological evaluation of indolyl bisphosphonates as anti-bone resorptive and anti-leishmanial agents Singh, Uma Sharan
 2008
 16 18 p. 8482-8491
10 p.
 artikel
43 Synthesis and biological evaluation of 2-(3′,4′,5′-trimethoxybenzoyl)-3-N,N-dimethylamino benzo[b]furan derivatives as inhibitors of tubulin polymerization Romagnoli, Romeo
 2008
 16 18 p. 8419-8426
8 p.
 artikel
44 Synthesis and biological properties of 2-methylene-19-nor-25-dehydro-1α-hydroxyvitamin D3-26,23-lactones—weak agonists Chiellini, Grazia
 2008
 16 18 p. 8563-8573
11 p.
 artikel
45 Synthesis and pharmacological evaluation of bis-3-(3,4-dichlorophenyl)acrylamide derivatives as glycogen phosphorylase inhibitors Onda, Kenichi
 2008
 16 18 p. 8627-8634
8 p.
 artikel
46 Synthesis and potent antileukemic activities of 10-benzyl-9(10H)-acridinones Gao, Chunmei
 2008
 16 18 p. 8670-8675
6 p.
 artikel
47 Synthesis, biological active molecular design, and molecular docking study of novel deazaflavin–cholestane hybrid compounds Shrestha, Ajaya R.
 2008
 16 18 p. 8685-8696
12 p.
 artikel
48 Synthesis, biological evaluation and SAR study of novel pyrazole analogues as inhibitors of Mycobacterium tuberculosis Castagnolo, Daniele
 2008
 16 18 p. 8587-8591
5 p.
 artikel
49 Synthesis of all-trans anandamide: A substrate for fatty acid amide hydrolase with dual effects on rabbit platelet activation Ferreri, Carla
 2008
 16 18 p. 8359-8365
7 p.
 artikel
50 Synthesis of highly selective fluorescent peptide probes for metal ions: Tuning selective metal monitoring with secondary structure Joshi, Bishnu Prasad
 2008
 16 18 p. 8501-8509
9 p.
 artikel
51 Synthesis of new indeno[1,2-e]pyrimido[4,5-b][1,4]diazepine-5,11-diones as potential antitumor agents Insuasty, Braulio
 2008
 16 18 p. 8492-8500
9 p.
 artikel
52 Synthesis of new 1-phenyl-3-{4-[(2E)-3-phenylprop-2-enoyl]phenyl}-thiourea and urea derivatives with anti-nociceptive activity dos Santos, Lorena
 2008
 16 18 p. 8526-8534
9 p.
 artikel
53 Synthesis of 3-phenylnaphthalenic derivatives as new selective MT2 melatoninergic ligands Poissonnier-Durieux, Sophie
 2008
 16 18 p. 8339-8348
10 p.
 artikel
54 Tetrahydropyridine-4-carboxamides as novel, potent transient receptor potential vanilloid 1 (TRPV1) antagonists Brown, Brian S.
 2008
 16 18 p. 8516-8525
10 p.
 artikel
55 Theoretical analysis of the electronic properties of the sex pheromone and its analogue derivatives in the female processionary moth Thaumetopoea pytiocampa Chamorro, Ester R.
 2008
 16 18 p. 8535-8545
11 p.
 artikel
56 The tert-butoxyl radical mediated hydrogen atom transfer reactions of the Parkinsonian proneurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine and selected tertiary amines Suleman, N. Kamrudin
 2008
 16 18 p. 8557-8562
6 p.
 artikel
                             56 gevonden resultaten
 
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