nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A new metabotropic glutamate receptor agonist with in vivo anti-allodynic activity
|
Stanley, Nathan J. |
|
2010 |
18 |
16 |
p. 6089-6098 10 p. |
artikel |
2 |
Anhydrotetracycline–peptide conjugates as representatives for ligand-based transactivating systems
|
Lochner, Susanne |
|
2010 |
18 |
16 |
p. 6127-6133 7 p. |
artikel |
3 |
Anti-HIV and antiplasmodial activity of original flavonoid derivatives
|
Casano, Gilles |
|
2010 |
18 |
16 |
p. 6012-6023 12 p. |
artikel |
4 |
Anti-Plasmodium activity of imidazolium and triazolium salts
|
Vlahakis, Jason Z. |
|
2010 |
18 |
16 |
p. 6184-6196 13 p. |
artikel |
5 |
A simple procedure for the derivation of electron density based surfaces of drug-receptor complexes from a combination of X-ray data and theoretical calculations
|
Mebs, Stefan |
|
2010 |
18 |
16 |
p. 5965-5974 10 p. |
artikel |
6 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2010 |
18 |
16 |
p. I-III nvt p. |
artikel |
7 |
Characterization of new PPARγ agonists: Benzimidazole derivatives—importance of positions 5 and 6, and computational studies on the binding mode
|
Goebel, Matthias |
|
2010 |
18 |
16 |
p. 5885-5895 11 p. |
artikel |
8 |
CLEFMA—An anti-proliferative curcuminoid from structure–activity relationship studies on 3,5-bis(benzylidene)-4-piperidones
|
Lagisetty, Pallavi |
|
2010 |
18 |
16 |
p. 6109-6120 12 p. |
artikel |
9 |
Comparison of MRI properties between derivatized DTPA and DOTA gadolinium–dendrimer conjugates
|
Nwe, K. |
|
2010 |
18 |
16 |
p. 5925-5931 7 p. |
artikel |
10 |
Concise synthesis of 5,6-dihydrovaltrate leading to enhanced Rev-export inhibitory congener
|
Tamura, Satoru |
|
2010 |
18 |
16 |
p. 5975-5980 6 p. |
artikel |
11 |
Design, synthesis, and anticonvulsant activity of new N-Mannich bases derived from spirosuccinimides and spirohydantoins
|
Obniska, Jolanta |
|
2010 |
18 |
16 |
p. 6134-6142 9 p. |
artikel |
12 |
Design, synthesis, and biological evaluation of ketoprofen analogs as potent cyclooxygenase-2 inhibitors
|
Zarghi, Afshin |
|
2010 |
18 |
16 |
p. 5855-5860 6 p. |
artikel |
13 |
Design, synthesis, and biological evaluation of prenylated chalcones as 5-LOX inhibitors
|
Reddy, Nimmanapalli P. |
|
2010 |
18 |
16 |
p. 5807-5815 9 p. |
artikel |
14 |
Dimethylaminopyridine derivatives of lupane triterpenoids are potent disruptors of mitochondrial structure and function
|
Holy, Jon |
|
2010 |
18 |
16 |
p. 6080-6088 9 p. |
artikel |
15 |
8,8-Dimethyldihydroberberine with improved bioavailability and oral efficacy on obese and diabetic mouse models
|
Cheng, Zhe |
|
2010 |
18 |
16 |
p. 5915-5924 10 p. |
artikel |
16 |
Dual inhibitors of inosine monophosphate dehydrogenase and histone deacetylase based on a cinnamic hydroxamic acid core structure
|
Chen, Liqiang |
|
2010 |
18 |
16 |
p. 5950-5964 15 p. |
artikel |
17 |
Editorial board
|
|
|
2010 |
18 |
16 |
p. IFC- 1 p. |
artikel |
18 |
Efficient synthesis and biological evaluation of demethyl geranylgeranoic acid derivatives
|
Wada, Akimori |
|
2010 |
18 |
16 |
p. 5795-5806 12 p. |
artikel |
19 |
Functional profiling of p53-binding sites in Hdm2 and Hdmx using a genetic selection system
|
Datta, Shreya |
|
2010 |
18 |
16 |
p. 6099-6108 10 p. |
artikel |
20 |
Further optimization of novel pyrrole 3-carboxamides for targeting serotonin 5-HT2A, 5-HT2C, and the serotonin transporter as a potential antidepressant
|
Kang, Suk Youn |
|
2010 |
18 |
16 |
p. 6156-6169 14 p. |
artikel |
21 |
Graphical contents list
|
|
|
2010 |
18 |
16 |
p. 5763-5774 12 p. |
artikel |
22 |
Improved inhibition of the histone acetyltransferase PCAF by an anacardic acid derivative
|
Ghizzoni, Massimo |
|
2010 |
18 |
16 |
p. 5826-5834 9 p. |
artikel |
23 |
Inactivation of protein tyrosine phosphatases by oltipraz and other cancer chemopreventive 1,2-dithiole-3-thiones
|
Bhattacharyya, Sanjib |
|
2010 |
18 |
16 |
p. 5945-5949 5 p. |
artikel |
24 |
Intramolecular acyl migration and enzymatic hydrolysis of a novel monoacylated ascorbic acid derivative, 6-O-dodecanoyl-2-O-α-d-glucopyranosyl-l-ascorbic acid
|
Tai, Akihiro |
|
2010 |
18 |
16 |
p. 6179-6183 5 p. |
artikel |
25 |
In vitro ADMET and physicochemical investigations of poly-N-methylated peptides designed to inhibit Aβ aggregation
|
Bose, Partha Pratim |
|
2010 |
18 |
16 |
p. 5896-5902 7 p. |
artikel |
26 |
Large flanking sequence effects in single nucleotide mismatch detection using fluorescent nucleoside Çf
|
Gardarsson, Haraldur |
|
2010 |
18 |
16 |
p. 6121-6126 6 p. |
artikel |
27 |
Lipophilic phenolic antioxidants: Correlation between antioxidant profile, partition coefficients and redox properties
|
Roleira, Fernanda M.F. |
|
2010 |
18 |
16 |
p. 5816-5825 10 p. |
artikel |
28 |
Multipotent drugs with cholinergic and neuroprotective properties for the treatment of Alzheimer and neuronal vascular diseases. I. Synthesis, biological assessment, and molecular modeling of simple and readily available 2-aminopyridine-, and 2-chloropyridine-3,5-dicarbonitriles
|
Samadi, Abdelouahid |
|
2010 |
18 |
16 |
p. 5861-5872 12 p. |
artikel |
29 |
Natural and semisynthetic azaphilones as a new scaffold for Hsp90 inhibitors
|
Musso, Loana |
|
2010 |
18 |
16 |
p. 6031-6043 13 p. |
artikel |
30 |
New bioactive halenaquinone derivatives from South Pacific marine sponges of the genus Xestospongia
|
Longeon, Arlette |
|
2010 |
18 |
16 |
p. 6006-6011 6 p. |
artikel |
31 |
New N-(phenoxydecyl)phthalimide derivatives displaying potent inhibition activity towards α-glucosidase
|
Pascale, Rossana |
|
2010 |
18 |
16 |
p. 5903-5914 12 p. |
artikel |
32 |
New porphyrin amino acid conjugates: Synthesis and photodynamic effect in human epithelial cells
|
Serra, V. Vaz |
|
2010 |
18 |
16 |
p. 6170-6178 9 p. |
artikel |
33 |
NMR spectroscopy and computational analysis of interaction between Serratia marcescens chitinase B and a dipeptide derived from natural-product cyclopentapeptide chitinase inhibitor argifin
|
Gouda, Hiroaki |
|
2010 |
18 |
16 |
p. 5835-5844 10 p. |
artikel |
34 |
Novel aminopeptidase N (APN/CD13) inhibitors derived from 3-phenylalanyl-N′-substituted-2,6-piperidinedione
|
Zhang, Xiaopan |
|
2010 |
18 |
16 |
p. 5981-5987 7 p. |
artikel |
35 |
Novel antifungal agents: Triazolopyridines as inhibitors of β-1,6-glucan synthesis
|
Kuroyanagi, Jun-ichi |
|
2010 |
18 |
16 |
p. 5845-5854 10 p. |
artikel |
36 |
Phenolic constituents isolated from Fragaria ananassa Duch. inhibit antigen-stimulated degranulation through direct inhibition of spleen tyrosine kinase activation
|
Ninomiya, Masayuki |
|
2010 |
18 |
16 |
p. 5932-5937 6 p. |
artikel |
37 |
Process R&D under the magnifying glass: Organization, business model, challenges, and scientific context
|
Federsel, Hans-Jürgen |
|
2010 |
18 |
16 |
p. 5775-5794 20 p. |
artikel |
38 |
Role of 2′,6′-dimethyl-l-tyrosine (Dmt) in some opioid lead compounds
|
Balboni, Gianfranco |
|
2010 |
18 |
16 |
p. 6024-6030 7 p. |
artikel |
39 |
Synergistic experimental/computational studies on arylazoenamine derivatives that target the bovine viral diarrhea virus RNA-dependent RNA polymerase
|
Giliberti, Gabriele |
|
2010 |
18 |
16 |
p. 6055-6068 14 p. |
artikel |
40 |
Syntheses and pharmacological characterization of novel thiazole derivatives as potential mGluR5 PET ligands
|
Baumann, Cindy A. |
|
2010 |
18 |
16 |
p. 6044-6054 11 p. |
artikel |
41 |
Synthesis and anti-hepatitis C virus activity of novel ethyl 1H-indole-3-carboxylates in vitro
|
Sellitto, Grazia |
|
2010 |
18 |
16 |
p. 6143-6148 6 p. |
artikel |
42 |
Synthesis, and biological evaluation of 2-(4-aminophenyl)benzothiazole derivatives as photosensitizing agents
|
Hu, Wan-Ping |
|
2010 |
18 |
16 |
p. 6197-6207 11 p. |
artikel |
43 |
Synthesis and biological evaluation of tetracyclic fluoroquinolones as antibacterial and anticancer agents
|
Al-Trawneh, Salah A. |
|
2010 |
18 |
16 |
p. 5873-5884 12 p. |
artikel |
44 |
Synthesis and T-type calcium channel blocking activity of novel diphenylpiperazine compounds, and evaluation of in vivo analgesic activity
|
Kam, Yoo Lim |
|
2010 |
18 |
16 |
p. 5938-5944 7 p. |
artikel |
45 |
Synthesis of aryl-heteroaryl ureas (AHUs) based on 4-aminoquinoline and their evaluation against the insulin-like growth factor receptor (IGF-1R)
|
Engen, William |
|
2010 |
18 |
16 |
p. 5995-6005 11 p. |
artikel |
46 |
Synthesis of novel 3,5-diaryl pyrazole derivatives using combinatorial chemistry as inhibitors of tyrosinase as well as potent anticancer, anti-inflammatory agents
|
Bandgar, Babasaheb P. |
|
2010 |
18 |
16 |
p. 6149-6155 7 p. |
artikel |
47 |
Synthesis of pyridazine and thiazole analogs as SGLT2 inhibitors
|
Kang, Suk Youn |
|
2010 |
18 |
16 |
p. 6069-6079 11 p. |
artikel |
48 |
The marine sponge metabolite mycothiazole: A novel prototype mitochondrial complex I inhibitor
|
Morgan, J. Brian |
|
2010 |
18 |
16 |
p. 5988-5994 7 p. |
artikel |