nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Active site mapping of trypsin, thrombin and matriptase-2 by sulfamoyl benzamidines
|
Dosa, Stefan |
|
2012 |
20 |
21 |
p. 6489-6505 17 p. |
artikel |
2 |
Adamantyl carboxamides and acetamides as potent human 11β-hydroxysteroid dehydrogenase type 1 inhibitors
|
Su, Xiangdong |
|
2012 |
20 |
21 |
p. 6394-6402 9 p. |
artikel |
3 |
A novel spirocyclic tropanyl-Δ2-isoxazoline derivative enhances citalopram and paroxetine binding to serotonin transporters as well as serotonin uptake
|
Dallanoce, Clelia |
|
2012 |
20 |
21 |
p. 6344-6355 12 p. |
artikel |
4 |
1,3-Azoles from ortho-naphthoquinones: Synthesis of aryl substituted imidazoles and oxazoles and their potent activity against Mycobacterium tuberculosis
|
Moura, Kelly C.G. |
|
2012 |
20 |
21 |
p. 6482-6488 7 p. |
artikel |
5 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2012 |
20 |
21 |
p. I-III nvt p. |
artikel |
6 |
Carbohydrate recognition by pentadecapeptide ligands for a series of sialylated oligosaccharides
|
Matsubara, Teruhiko |
|
2012 |
20 |
21 |
p. 6452-6458 7 p. |
artikel |
7 |
Conformational analysis of two novel cytotoxic C2-substituted pyrrolo[2,3-f]quinolines in aqueous media, organic solvents, membrane bilayers and at the putative active site
|
Varvarigou, Nicole |
|
2012 |
20 |
21 |
p. 6276-6284 9 p. |
artikel |
8 |
Design, synthesis and biological evaluation of heterocyclic azoles derivatives containing pyrazine moiety as potential telomerase inhibitors
|
Zhang, Yan-Bin |
|
2012 |
20 |
21 |
p. 6356-6365 10 p. |
artikel |
9 |
Design, synthesis and in vitro evaluation of a series of α-substituted phenylpropanoic acid PPARγ agonists to further investigate the stereochemistry–activity relationship
|
Ohashi, Masao |
|
2012 |
20 |
21 |
p. 6375-6383 9 p. |
artikel |
10 |
Development and characterization of endocannabinoid hydrolases FAAH and MAGL inhibitors bearing a benzotriazol-1-yl carboxamide scaffold
|
Morera, Ludovica |
|
2012 |
20 |
21 |
p. 6260-6275 16 p. |
artikel |
11 |
Editorial board
|
|
|
2012 |
20 |
21 |
p. IFC- 1 p. |
artikel |
12 |
Graphical contents list
|
|
|
2012 |
20 |
21 |
p. 6199-6207 9 p. |
artikel |
13 |
Identification of a 2-phenyl-substituted octahydrobenzo[f]quinoline as a dopamine D3 receptor-selective full agonist ligand
|
Clark, Alia H. |
|
2012 |
20 |
21 |
p. 6366-6374 9 p. |
artikel |
14 |
Improving the affinity of naphthalene diimide ligand to telomeric DNA by incorporating Zn2+ ions into its dipicolylamine groups
|
Czerwinska, Izabella |
|
2012 |
20 |
21 |
p. 6416-6422 7 p. |
artikel |
15 |
Lead optimization studies towards the discovery of novel carbamates as potent AChE inhibitors for the potential treatment of Alzheimer’s disease
|
Roy, Kuldeep K. |
|
2012 |
20 |
21 |
p. 6313-6320 8 p. |
artikel |
16 |
New prenylated isoflavonoids as protein tyrosine phosphatase 1B (PTP1B) inhibitors from Erythrina addisoniae
|
Nguyen, Phi Hung |
|
2012 |
20 |
21 |
p. 6459-6464 6 p. |
artikel |
17 |
Novel multipotent phenylthiazole–tacrine hybrids for the inhibition of cholinesterase activity, β-amyloid aggregation and Ca2+ overload
|
Wang, Yue |
|
2012 |
20 |
21 |
p. 6513-6522 10 p. |
artikel |
18 |
Optimization of anti-Trypanosoma cruzi oxadiazoles leads to identification of compounds with efficacy in infected mice
|
dos Santos Filho, José Maurício |
|
2012 |
20 |
21 |
p. 6423-6433 11 p. |
artikel |
19 |
Potent small molecule Hedgehog agonists induce VEGF expression in vitro
|
Seifert, Katrin |
|
2012 |
20 |
21 |
p. 6465-6481 17 p. |
artikel |
20 |
Pyrido[1,2-a]pyrimidin-4-ones as antiplasmodial falcipain-2 inhibitors
|
Mane, U.R. |
|
2012 |
20 |
21 |
p. 6296-6304 9 p. |
artikel |
21 |
Role of the side chain stereochemistry in the α-glucosidase inhibitory activity of kotalanol, a potent natural α-glucosidase inhibitor. Part 2
|
Tanabe, Genzoh |
|
2012 |
20 |
21 |
p. 6321-6334 14 p. |
artikel |
22 |
Search for anticonvulsant and analgesic active derivatives of dihydrofuran-2(3H)-one
|
Więckowski, Krzysztof |
|
2012 |
20 |
21 |
p. 6533-6544 12 p. |
artikel |
23 |
Small-molecular inhibitors of Ca2+-induced mitochondrial permeability transition (MPT) derived from muscle relaxant dantrolene
|
Murasawa, Shinpei |
|
2012 |
20 |
21 |
p. 6384-6393 10 p. |
artikel |
24 |
Structure–activity relationship study of pyrimido[1,2-c][1,3]benzothiazin-6-imine derivatives for potent anti-HIV agents
|
Mizuhara, Tsukasa |
|
2012 |
20 |
21 |
p. 6434-6441 8 p. |
artikel |
25 |
Synthesis and antifungal activity of diverse C-2 pyridinyl and pyridinylvinyl substituted quinolines
|
Kouznetsov, Vladimir V. |
|
2012 |
20 |
21 |
p. 6506-6512 7 p. |
artikel |
26 |
Synthesis and biological evaluation of a series of podophyllotoxins derivatives as a class of potent antitubulin agents
|
Liu, Yingqian |
|
2012 |
20 |
21 |
p. 6285-6295 11 p. |
artikel |
27 |
Synthesis and structure–activity relationship of fused-pyrimidine derivatives as a series of novel GPR119 agonists
|
Negoro, Kenji |
|
2012 |
20 |
21 |
p. 6442-6451 10 p. |
artikel |
28 |
Synthesis, biological activity and structure–activity relationship of endomorphin-1/substance P derivatives
|
Varamini, Pegah |
|
2012 |
20 |
21 |
p. 6335-6343 9 p. |
artikel |
29 |
Synthesis of a potent photoreactive acidic γ-secretase modulator for target identification in cells
|
Rennhack, Andreas |
|
2012 |
20 |
21 |
p. 6523-6532 10 p. |
artikel |
30 |
Synthesis of 1,5-diarylhaloimidazole analogs and their inhibitory activities against PGE2 production from LPS-treated RAW 264.7 cells
|
Yang, Zunhua |
|
2012 |
20 |
21 |
p. 6256-6259 4 p. |
artikel |
31 |
Synthesis of imidacloprid derivatives with a chiral alkylated imidazolidine ring and evaluation of their insecticidal activity and affinity to the nicotinic acetylcholine receptor
|
Nishiwaki, Hisashi |
|
2012 |
20 |
21 |
p. 6305-6312 8 p. |
artikel |
32 |
Synthesis of Staphylococcus aureus type 5 capsular polysaccharide repeating unit using novel l-FucNAc and d-FucNAc synthons and immunochemical evaluation
|
Danieli, Elisa |
|
2012 |
20 |
21 |
p. 6403-6415 13 p. |
artikel |
33 |
Tandem photoaffinity labeling–bioorthogonal conjugation in medicinal chemistry
|
Lapinsky, David J. |
|
2012 |
20 |
21 |
p. 6237-6247 11 p. |
artikel |
34 |
The antitumor agent doxorubicin binds to Fanconi anemia group F protein
|
Kusayanagi, Tomoe |
|
2012 |
20 |
21 |
p. 6248-6255 8 p. |
artikel |
35 |
The therapeutic journey of benzimidazoles: A review
|
Bansal, Yogita |
|
2012 |
20 |
21 |
p. 6208-6236 29 p. |
artikel |