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                             36 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A comparison of DNA and RNA quadruplex structures and stabilities Joachimi, Astrid
 2009
 17 19 p. 6811-6815
5 p.
 artikel
2 A new therapeutic approach in Parkinson’s disease: Some novel quinazoline derivatives as dual selective phosphodiesterase 1 inhibitors and anti-inflammatory agents Laddha, Sachin S.
 2009
 17 19 p. 6796-6802
7 p.
 artikel
3 Application of the McMurry coupling reaction in the synthesis of tri- and tetra-arylethylene analogues as potential cancer chemotherapeutic agents Tanpure, Rajendra P.
 2009
 17 19 p. 6993-7001
9 p.
 artikel
4 A SPR strategy for high-throughput ligand screenings based on synthetic peptides mimicking a selected subdomain of the target protein: A proof of concept on HER2 receptor Monfregola, Luca
 2009
 17 19 p. 7015-7020
6 p.
 artikel
5 Comparative molecular field analysis and synthetic validation of a hydroxyamide-propofol binding and functional block of neuronal voltage-dependent sodium channels Brown, Milton L.
 2009
 17 19 p. 7056-7063
8 p.
 artikel
6 Computational modeling of novel inhibitors targeting the Akt pleckstrin homology domain Du-Cuny, Lei
 2009
 17 19 p. 6983-6992
10 p.
 artikel
7 Design of a bioreductively-activated fluorescent pH probe for tumor hypoxia imaging Nakata, Eiji
 2009
 17 19 p. 6952-6958
7 p.
 artikel
8 Design, synthesis and biological evaluation of tripeptide boronic acid proteasome inhibitors Zhu, Yongqiang
 2009
 17 19 p. 6851-6861
11 p.
 artikel
9 Design, synthesis and biological evaluations of novel 7-[3-(1-aminocycloalkyl)pyrrolidin-1-yl]-6-desfluoro-8-methoxyquinolones with potent antibacterial activity against multi-drug resistant Gram-positive bacteria Miyauchi, Rie
 2009
 17 19 p. 6879-6889
11 p.
 artikel
10 Design, synthesis and structure–activity relationship of 2-(3′,4′,5′-trimethoxybenzoyl)-benzo[b]furan derivatives as a novel class of inhibitors of tubulin polymerization Romagnoli, Romeo
 2009
 17 19 p. 6862-6871
10 p.
 artikel
11 Dibenzazecine scaffold rebuilding—Is the flexibility always essential for high dopamine receptor affinities? Schulze, Maria
 2009
 17 19 p. 6898-6907
10 p.
 artikel
12 δ-Di-carboxybutyl phosphoramidate of 2′-deoxycytidine-5′-monophosphate as substrate for DNA polymerization by HIV-1 reverse transcriptase Zlatev, Ivan
 2009
 17 19 p. 7008-7014
7 p.
 artikel
13 Discovery of trans-N-[1-(2-fluorophenyl)-3-pyrazolyl]-3-oxospiro[6-azaisobenzofuran-1(3H),1′-cyclohexane]-4′-carboxamide, a potent and orally active neuropeptide Y Y5 receptor antagonist Haga, Yuji
 2009
 17 19 p. 6971-6982
12 p.
 artikel
14 Editorial board 2009
 17 19 p. IFC-
1 p.
 artikel
15 Erratum to “Hydrazinocurcumin, a novel synthetic curcumin derivative, is a potent inhibitor of endothelial cell proliferation” [Bioorg. Med. Chem. 10 (2002) (2987–2992)] Shim, Joong Sup
 2009
 17 19 p. 7073-
1 p.
 artikel
16 Furanocoumarins: Novel topoisomerase I inhibitors from Ruta graveolens L. Diwan, Renuka
 2009
 17 19 p. 7052-7055
4 p.
 artikel
17 Graphical contents list 2009
 17 19 p. 6787-6795
9 p.
 artikel
18 Identification and characterization of novel sirtuin inhibitor scaffolds Sanders, Brandi D.
 2009
 17 19 p. 7031-7041
11 p.
 artikel
19 Identification of small molecule regulators of the nuclear receptor HNF4α based on naphthofuran scaffolds Le Guével, Rémy
 2009
 17 19 p. 7021-7030
10 p.
 artikel
20 Inhibition of serotonin and norepinephrine reuptake and inhibition of phosphodiesterase by multi-target inhibitors as potential agents for depression Cashman, John R.
 2009
 17 19 p. 6890-6897
8 p.
 artikel
21 Instructions to contributors 2009
 17 19 p. I-
1 p.
 artikel
22 Ligand-based design and synthesis of novel sodium channel blockers from a combined phenytoin–lidocaine pharmacophore Wang, Yuesheng
 2009
 17 19 p. 7064-7072
9 p.
 artikel
23 Neuraminidase inhibitory activities of flavonols isolated from Rhodiola rosea roots and their in vitro anti-influenza viral activities Jeong, Hyung Jae
 2009
 17 19 p. 6816-6823
8 p.
 artikel
24 New potent P-glycoprotein modulators with the cucurbitane scaffold and their synergistic interaction with doxorubicin on resistant cancer cells Ramalhete, Cátia
 2009
 17 19 p. 6942-6951
10 p.
 artikel
25 Novel 7H-pyrrolo[2,3-d]pyrimidine derivatives as potent and orally active STAT6 inhibitors Nagashima, Shinya
 2009
 17 19 p. 6926-6936
11 p.
 artikel
26 Push–pull benzothiazole derivatives as probes for detecting β-amyloid plaques in Alzheimer’s brains Ono, Masahiro
 2009
 17 19 p. 7002-7007
6 p.
 artikel
27 Rapid isolation of novel FK506 binding proteins from multiple organisms using gDNA and cDNA T7 phage display Piggott, Andrew M.
 2009
 17 19 p. 6841-6850
10 p.
 artikel
28 Rational design and synthesis of highly potent anti-acetylcholinesterase activity huperzine A derivatives Yan, Jian
 2009
 17 19 p. 6937-6941
5 p.
 artikel
29 Recognition of CG interrupting site by W-shaped nucleoside analogs (WNA) having the pyrazole ring in an anti-parallel triplex DNA Taniguchi, Yosuke
 2009
 17 19 p. 6803-6810
8 p.
 artikel
30 Synthesis and biological evaluation of novel phthalazinone derivatives as topically active phosphodiesterase 4 inhibitors Kagayama, Kohei
 2009
 17 19 p. 6959-6970
12 p.
 artikel
31 Synthesis and biological evaluation of 2,3,4-triarylbenzopyran derivatives as SERM and therapeutic agent for breast cancer Kumar, Shailesh
 2009
 17 19 p. 6832-6840
9 p.
 artikel
32 Synthesis and dopaminergic activity of some E-3-(piperidin-1-yl)-1-(4-substituted phenyl)prop-2-en-1-one derivatives Sakhteman, Amirhossein
 2009
 17 19 p. 6908-6913
6 p.
 artikel
33 Synthesis and in vitro activities of new anticancer duplex drugs linking 2′-deoxy-5-fluorouridine (5-FdU) with 3′-C-ethynylcytidine (ECyd) via a phosphodiester bonding Schott, Herbert
 2009
 17 19 p. 6824-6831
8 p.
 artikel
34 Synthesis of heteroaromatic tropeines and heterogeneous binding to glycine receptors Maksay, Gábor
 2009
 17 19 p. 6872-6878
7 p.
 artikel
35 The design and optimization of a series of 2-(pyridin-2-yl)-1H-benzimidazole compounds as allosteric glucokinase activators Takahashi, Keiji
 2009
 17 19 p. 7042-7051
10 p.
 artikel
36 Thienylhalomethylketones: Irreversible glycogen synthase kinase 3 inhibitors as useful pharmacological tools Perez, Daniel I.
 2009
 17 19 p. 6914-6925
12 p.
 artikel
                             36 gevonden resultaten
 
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