| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acetyl analogs of combretastatin A-4: Synthesis and biological studies
|
Babu, Balaji
|
|
2011
|
19 |
7 |
p. 2359-2367
9 p.
|
artikel
|
| 2 |
Arsonic acid-presenting superparamagnetic iron oxide for pH-responsive aggregation under slightly acidic conditions
|
Minehara, Hiroki
|
|
2011
|
19 |
7 |
p. 2282-2286
5 p.
|
artikel
|
| 3 |
Assessing high affinity binding to HLA-DQ2.5 by a novel peptide library based approach
|
Jüse, Ulrike
|
|
2011
|
19 |
7 |
p. 2470-2477
8 p.
|
artikel
|
| 4 |
β-Branched acyclic nucleoside analogues as inhibitors of Plasmodium falciparum dUTPase
|
Baragaña, Beatriz
|
|
2011
|
19 |
7 |
p. 2378-2391
14 p.
|
artikel
|
| 5 |
Contribution of cinnamic acid analogues in rosmarinic acid to inhibition of snake venom induced hemorrhage
|
Aung, Hnin Thanda
|
|
2011
|
19 |
7 |
p. 2392-2396
5 p.
|
artikel
|
| 6 |
Controlled-release system of single-stranded DNA triggered by the photothermal effect of gold nanorods and its in vivo application
|
Yamashita, Shuji
|
|
2011
|
19 |
7 |
p. 2130-2135
6 p.
|
artikel
|
| 7 |
CyDEPMPOs: A class of stable cyclic DEPMPO derivatives with improved properties as mechanistic markers of stereoselective hydroxyl radical adduct formation in biological systems
|
Gosset, Gaëlle
|
|
2011
|
19 |
7 |
p. 2218-2230
13 p.
|
artikel
|
| 8 |
Design, synthesis and biological activity of thiazolidine-4-carboxylic acid derivatives as novel influenza neuraminidase inhibitors
|
Liu, Yu
|
|
2011
|
19 |
7 |
p. 2342-2348
7 p.
|
artikel
|
| 9 |
Design, synthesis and structure–activity relationship (SAR) studies of 2,4-disubstituted pyrimidine derivatives: Dual activity as cholinesterase and Aβ-aggregation inhibitors
|
Mohamed, Tarek
|
|
2011
|
19 |
7 |
p. 2269-2281
13 p.
|
artikel
|
| 10 |
Desulfurization of 2-thiouracil nucleosides: Conformational studies of 4-pyrimidinone nucleosides
|
Kraszewska, Karina
|
|
2011
|
19 |
7 |
p. 2443-2449
7 p.
|
artikel
|
| 11 |
Dihydro-β-agarofuran sesquiterpenes isolated from Celastrus vulcanicola as potential anti-Mycobacterium tuberculosis multidrug-resistant agents
|
Torres-Romero, David
|
|
2011
|
19 |
7 |
p. 2182-2189
8 p.
|
artikel
|
| 12 |
4D-QSAR analysis and pharmacophore modeling: Electron conformational-genetic algorithm approach for penicillins
|
Yanmaz, Ersin
|
|
2011
|
19 |
7 |
p. 2199-2210
12 p.
|
artikel
|
| 13 |
Editorial board
|
|
|
2011
|
19 |
7 |
p. IFC-
1 p.
|
artikel
|
| 14 |
Exploration of larger central ring linkers in furamidine analogues: Synthesis and evaluation of their DNA binding, antiparasitic and fluorescence properties
|
Farahat, Abdelbasset A.
|
|
2011
|
19 |
7 |
p. 2156-2167
12 p.
|
artikel
|
| 15 |
Graphical contents list
|
|
|
2011
|
19 |
7 |
p. 2103-2113
11 p.
|
artikel
|
| 16 |
17,20-Lyase inhibitors. Part 3: Design, synthesis, and structure–activity relationships of biphenylylmethylimidazole derivatives as novel 17,20-lyase inhibitors
|
Kaku, Tomohiro
|
|
2011
|
19 |
7 |
p. 2428-2442
15 p.
|
artikel
|
| 17 |
Lysine proximity significantly affects glycation of lysine-containing collagen model peptides
|
Kitamura, Asuka
|
|
2011
|
19 |
7 |
p. 2125-2129
5 p.
|
artikel
|
| 18 |
Methylation-mediated control of aurora kinase B and Haspin with epigenetically modified histone H3 N-terminal peptides
|
Han, Areum
|
|
2011
|
19 |
7 |
p. 2373-2377
5 p.
|
artikel
|
| 19 |
Microbial transformation of (+)-nootkatone and the antiproliferative activity of its metabolites
|
Gliszczyńska, Anna
|
|
2011
|
19 |
7 |
p. 2464-2469
6 p.
|
artikel
|
| 20 |
5′-Modified pyrimidine nucleosides as inhibitors of ribonuclease A
|
Samanta, Anirban
|
|
2011
|
19 |
7 |
p. 2478-2484
7 p.
|
artikel
|
| 21 |
Molecular properties affecting fast dissociation from the D2 receptor
|
Tresadern, Gary
|
|
2011
|
19 |
7 |
p. 2231-2241
11 p.
|
artikel
|
| 22 |
Non-peptide NK1 receptor ligands based on the 4-phenylpyridine moiety
|
Giuliani, Germano
|
|
2011
|
19 |
7 |
p. 2242-2251
10 p.
|
artikel
|
| 23 |
Per-N-methylated analogues of an antitumor bicyclic hexapeptide RA-VII
|
Hitotsuyanagi, Yukio
|
|
2011
|
19 |
7 |
p. 2458-2463
6 p.
|
artikel
|
| 24 |
Pyrrolo[3,4-h]quinolinones a new class of photochemotherapeutic agents
|
Barraja, Paola
|
|
2011
|
19 |
7 |
p. 2326-2341
16 p.
|
artikel
|
| 25 |
Radiosynthesis and in vivo evaluation of 1-[18F]fluoroelacridar as a positron emission tomography tracer for P-glycoprotein and breast cancer resistance protein
|
Dörner, Bernd
|
|
2011
|
19 |
7 |
p. 2190-2198
9 p.
|
artikel
|
| 26 |
Radiosynthesis of the tumor hypoxia marker [18F]TFMISO via O-[18F]trifluoroethylation reveals a striking difference between trifluoroethyl tosylate and iodide in regiochemical reactivity toward oxygen nucleophiles
|
Suehiro, Makiko
|
|
2011
|
19 |
7 |
p. 2287-2297
11 p.
|
artikel
|
| 27 |
Role of the side chain stereochemistry in the α-glucosidase inhibitory activity of kotalanol, a potent natural α-glucosidase inhibitor
|
Xie, Weijia
|
|
2011
|
19 |
7 |
p. 2252-2262
11 p.
|
artikel
|
| 28 |
Selective biocatalytic aminolysis of (±)-epichlorohydrin: Synthesis and ICAM-1 inhibitory activity of (S)-(+)-3-arylamino-1-chloropropan-2-ols
|
Gupta, Pankaj
|
|
2011
|
19 |
7 |
p. 2263-2268
6 p.
|
artikel
|
| 29 |
Structure–activity relationships in a series of C2-substituted gluco-configured tetrahydroimidazopyridines as β-glucosidase inhibitors
|
Li, Tiehai
|
|
2011
|
19 |
7 |
p. 2136-2144
9 p.
|
artikel
|
| 30 |
Syntheses of 2-deoxy-2,3-didehydro-N-acetylneuraminic acid analogues modified by N-sulfonylamidino groups at the C-4 position and biological evaluation as inhibitors of human parainfluenza virus type 1
|
Nishino, Reiko
|
|
2011
|
19 |
7 |
p. 2418-2427
10 p.
|
artikel
|
| 31 |
Synthesis and anti-melanogenic activity of hydroxyphenyl benzyl ether analogues
|
Sapkota, Kiran
|
|
2011
|
19 |
7 |
p. 2168-2175
8 p.
|
artikel
|
| 32 |
Synthesis and antiviral activity of N 9-[3-fluoro-2-(phosphonomethoxy)propyl] analogues derived from N 6-substituted adenines and 2,6-diaminopurines
|
Baszczyňski, Ondřej
|
|
2011
|
19 |
7 |
p. 2114-2124
11 p.
|
artikel
|
| 33 |
Synthesis and biological evaluation of new 2-alkylaminoethyl-1,1-bisphosphonic acids against Trypanosoma cruzi and Toxoplasma gondii targeting farnesyl diphosphate synthase
|
Rosso, Valeria S.
|
|
2011
|
19 |
7 |
p. 2211-2217
7 p.
|
artikel
|
| 34 |
Synthesis and biological evaluation of novel irreversible serine protease inhibitors using amino acid based sulfonyl fluorides as an electrophilic trap
|
Brouwer, Arwin J.
|
|
2011
|
19 |
7 |
p. 2397-2406
10 p.
|
artikel
|
| 35 |
Synthesis and evaluation of cardiac glycoside mimics as potential anticancer drugs
|
Jensen, Marie
|
|
2011
|
19 |
7 |
p. 2407-2417
11 p.
|
artikel
|
| 36 |
Synthesis and in vivo evaluation of (S)-6-(4-fluorophenoxy)-3-((1-[11C]methylpiperidin-3-yl)methyl)-2-o-tolylquinazolin-4(3H)-one, a potential PET tracer for growth hormone secretagogue receptor (GHSR)
|
Potter, Rachel
|
|
2011
|
19 |
7 |
p. 2368-2372
5 p.
|
artikel
|
| 37 |
Synthesis, biological evaluation and molecular modeling of novel triazole-containing berberine derivatives as acetylcholinesterase and β-amyloid aggregation inhibitors
|
Shi, Anding
|
|
2011
|
19 |
7 |
p. 2298-2305
8 p.
|
artikel
|
| 38 |
Synthesis, evaluation and structural studies of antiproliferative tubulin-targeting azetidin-2-ones
|
O’Boyle, Niamh M.
|
|
2011
|
19 |
7 |
p. 2306-2325
20 p.
|
artikel
|
| 39 |
Synthesis of a new 4-aza-2,3-didehydropodophyllotoxin analogues as potent cytotoxic and antimitotic agents
|
Kamal, Ahmed
|
|
2011
|
19 |
7 |
p. 2349-2358
10 p.
|
artikel
|
| 40 |
Synthesis of 68Ga-labeled DOTA-nitroimidazole derivatives and their feasibilities as hypoxia imaging PET tracers
|
Hoigebazar, Lathika
|
|
2011
|
19 |
7 |
p. 2176-2181
6 p.
|
artikel
|
| 41 |
Synthesis of rabdokunmin C analogues and their inhibitory effect on NF-κB activation
|
Aoyagi, Yutaka
|
|
2011
|
19 |
7 |
p. 2450-2457
8 p.
|
artikel
|
| 42 |
Using small molecules to target protein phosphatases
|
Vintonyak, Viktor V.
|
|
2011
|
19 |
7 |
p. 2145-2155
11 p.
|
artikel
|
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