| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
2-Amino-4-methyl-5-phenylethyl substituted-7-N-benzyl-pyrrolo[2,3-d]pyrimidines as novel antitumor antimitotic agents that also reverse tumor resistance
|
Gangjee, Aleem
|
|
2011
|
19 |
14 |
p. 4355-4365
11 p.
|
artikel
|
| 2 |
Design and synthesis of 4-amino-2-phenylquinazolines as novel topoisomerase I inhibitors with molecular modeling
|
Le, Thanh Nguyen
|
|
2011
|
19 |
14 |
p. 4399-4404
6 p.
|
artikel
|
| 3 |
Design, synthesis and antileishmanial in vitro activity of new series of chalcones-like compounds: A molecular hybridization approach
|
Barbosa, Ticiano P.
|
|
2011
|
19 |
14 |
p. 4250-4256
7 p.
|
artikel
|
| 4 |
Design, synthesis and biological evaluation of 2′-deoxy-2′,2′-difluoro-5-halouridine phosphoramidate ProTides
|
Quintiliani, Maurizio
|
|
2011
|
19 |
14 |
p. 4338-4345
8 p.
|
artikel
|
| 5 |
Discovery and evaluation of 3-phenyl-1H-5-pyrazolylamine-based derivatives as potent, selective and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)
|
Lin, Wen-Hsing
|
|
2011
|
19 |
14 |
p. 4173-4182
10 p.
|
artikel
|
| 6 |
Editorial board
|
|
|
2011
|
19 |
14 |
p. IFC-
1 p.
|
artikel
|
| 7 |
5-Ethynyl-1-β-d-ribofuranosyl-1H-[1,2,3]triazole-4-carboxylic acid amide (ETCAR) and its analogues: Synthesis and cytotoxic properties
|
Ostrowski, Tomasz
|
|
2011
|
19 |
14 |
p. 4386-4398
13 p.
|
artikel
|
| 8 |
Generation of ‘Unnatural Natural Product’ library and identification of a small molecule inhibitor of XIAP
|
Kawamura, Tatsuro
|
|
2011
|
19 |
14 |
p. 4377-4385
9 p.
|
artikel
|
| 9 |
18β-Glycyrrhetinic acid derivatives induced mitochondrial-mediated apoptosis through reactive oxygen species-mediated p53 activation in NTUB1 cells
|
Lin, Kai-Wei
|
|
2011
|
19 |
14 |
p. 4274-4285
12 p.
|
artikel
|
| 10 |
G-quadruplex DNA aptamers generated for systemin
|
Bing, Tao
|
|
2011
|
19 |
14 |
p. 4211-4219
9 p.
|
artikel
|
| 11 |
Graphical contents list
|
|
|
2011
|
19 |
14 |
p. 4155-4161
7 p.
|
artikel
|
| 12 |
Imidazo[1,2-a]pyridin-3-amines as potential HIV-1 non-nucleoside reverse transcriptase inhibitors
|
Bode, Moira L.
|
|
2011
|
19 |
14 |
p. 4227-4237
11 p.
|
artikel
|
| 13 |
Interactions of the carrier ligands of antidiabetic metal complexes with human serum albumin: A combined spectroscopic and separation approach with molecular modeling studies
|
Enyedy, Éva A.
|
|
2011
|
19 |
14 |
p. 4202-4210
9 p.
|
artikel
|
| 14 |
Phenylimino-10H-anthracen-9-ones as novel antimicrotubule agents—synthesis, antiproliferative activity and inhibition of tubulin polymerization
|
Prinz, Helge
|
|
2011
|
19 |
14 |
p. 4183-4191
9 p.
|
artikel
|
| 15 |
Probes for narcotic receptor mediated phenomena. 43. Synthesis of the ortho-a and para-a, and improved synthesis and optical resolution of the ortho-b and para-b oxide-bridged phenylmorphans: Compounds with moderate to low opioid-receptor affinity
|
Li, Feng
|
|
2011
|
19 |
14 |
p. 4330-4337
8 p.
|
artikel
|
| 16 |
Synthesis and antidepressant-like activity evaluation of sulphonamides and sulphonyl-hydrazones
|
de Oliveira, Kely Navakoski
|
|
2011
|
19 |
14 |
p. 4295-4306
12 p.
|
artikel
|
| 17 |
Synthesis and biological evaluation of naphthyl phenyl ethers (NPEs) as novel nonnucleoside HIV-1 reverse transcriptase inhibitors
|
Gu, Shuang-Xi
|
|
2011
|
19 |
14 |
p. 4220-4226
7 p.
|
artikel
|
| 18 |
Synthesis and biological evaluation of novel 5-alkyl-2-arylthio-6-((3,4-dihydroquinolin-1(2H)-yl)methyl)pyrimidin-4(3H)-ones as potent non-nucleoside HIV-1 reverse transcriptase inhibitors
|
Zhang, Jing
|
|
2011
|
19 |
14 |
p. 4366-4376
11 p.
|
artikel
|
| 19 |
Synthesis and evaluation of a radioiodinated trisaccharide derivative as a synthetic substrate for a sensitive N-acetylglucosaminyltransferase V radioassay
|
Mukai, Takahiro
|
|
2011
|
19 |
14 |
p. 4312-4321
10 p.
|
artikel
|
| 20 |
Synthesis and evaluation of bidentate ligands designed to interact with PDZ domains
|
Boucherle, Benjamin
|
|
2011
|
19 |
14 |
p. 4346-4354
9 p.
|
artikel
|
| 21 |
Synthesis and evaluation of hermitamides A and B as human voltage-gated sodium channel blockers
|
De Oliveira, Eliseu O.
|
|
2011
|
19 |
14 |
p. 4322-4329
8 p.
|
artikel
|
| 22 |
Synthesis and structure–activity relationship of new 1,5-dialkyl-1,5-benzodiazepines as cholecystokinin-2 receptor antagonists
|
Roberts, Karen
|
|
2011
|
19 |
14 |
p. 4257-4273
17 p.
|
artikel
|
| 23 |
Synthesis, biological evaluation and docking studies of octane-carboxamide based renin inhibitors with extended segments toward S3′ site of renin
|
Wu, Yong
|
|
2011
|
19 |
14 |
p. 4238-4249
12 p.
|
artikel
|
| 24 |
Synthesis of new series of α-cyclodextrin esters as dopamine carrier molecule
|
Seyedi, Seyed Mohammad
|
|
2011
|
19 |
14 |
p. 4307-4311
5 p.
|
artikel
|
| 25 |
Synthesis of novel inhibitors of β-glucuronidase based on benzothiazole skeleton and study of their binding affinity by molecular docking
|
Khan, Khalid Mohammed
|
|
2011
|
19 |
14 |
p. 4286-4294
9 p.
|
artikel
|
| 26 |
The discovery of long-acting saligenin β2 adrenergic receptor agonists incorporating hydantoin or uracil rings
|
Procopiou, Panayiotis A.
|
|
2011
|
19 |
14 |
p. 4192-4201
10 p.
|
artikel
|
| 27 |
Transformation of thiols to disulfides by epolactaene and its derivatives
|
Kuramochi, Kouji
|
|
2011
|
19 |
14 |
p. 4162-4172
11 p.
|
artikel
|
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