| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acyl derivatives of p-aminosulfonamides and dapsone as new inhibitors of the arginine methyltransferase hPRMT1
|
Bissinger, Elisabeth-Maria
|
|
2011
|
19 |
12 |
p. 3717-3731
15 p.
|
artikel
|
| 2 |
After the grape rush: Sirtuins as epigenetic drug targets in neurodegenerative disorders
|
Huber, Kilian
|
|
2011
|
19 |
12 |
p. 3616-3624
9 p.
|
artikel
|
| 3 |
An investigation of phenylthiazole antiflaviviral agents
|
Mayhoub, Abdelrahman S.
|
|
2011
|
19 |
12 |
p. 3845-3854
10 p.
|
artikel
|
| 4 |
Biological activity of water-soluble inclusion complexes of 1′-acetoxychavicol acetate with cyclodextrins
|
Azuma, Hideki
|
|
2011
|
19 |
12 |
p. 3855-3863
9 p.
|
artikel
|
| 5 |
Characterization of chemical, radiochemical and optical properties of a dual-labeled MMP-9 targeting peptide
|
Azhdarinia, Ali
|
|
2011
|
19 |
12 |
p. 3769-3776
8 p.
|
artikel
|
| 6 |
Computer- and structure-based lead design for epigenetic targets
|
Heinke, Ralf
|
|
2011
|
19 |
12 |
p. 3605-3615
11 p.
|
artikel
|
| 7 |
Conformational variability of different sulfonamide inhibitors with thienyl-acetamido moieties attributes to differential binding in the active site of cytosolic human carbonic anhydrase isoforms
|
Biswas, Shyamasri
|
|
2011
|
19 |
12 |
p. 3732-3738
7 p.
|
artikel
|
| 8 |
Deglycobleomycin A6 analogues modified in the methylvalerate moiety
|
Cai, Xiaoqing
|
|
2011
|
19 |
12 |
p. 3831-3844
14 p.
|
artikel
|
| 9 |
DOTA derivatives for site-specific biomolecule-modification via click chemistry: Synthesis and comparison of reaction characteristics
|
Wängler, Carmen
|
|
2011
|
19 |
12 |
p. 3864-3874
11 p.
|
artikel
|
| 10 |
Editorial board
|
|
|
2011
|
19 |
12 |
p. IFC-
1 p.
|
artikel
|
| 11 |
Enantioselective synthesis of tranylcypromine analogues as lysine demethylase (LSD1) inhibitors
|
Benelkebir, Hanae
|
|
2011
|
19 |
12 |
p. 3709-3716
8 p.
|
artikel
|
| 12 |
Epigenetic drug discovery special issue
|
Sippl, Wolfgang
|
|
2011
|
19 |
12 |
p. 3603-3604
2 p.
|
artikel
|
| 13 |
Epigenetic profiling of the antitumor natural product psammaplin A and its analogues
|
García, José
|
|
2011
|
19 |
12 |
p. 3637-3649
13 p.
|
artikel
|
| 14 |
Extraction of tacit knowledge from large ADME data sets via pairwise analysis
|
Keefer, Christopher E.
|
|
2011
|
19 |
12 |
p. 3739-3749
11 p.
|
artikel
|
| 15 |
Graphical contents list
|
|
|
2011
|
19 |
12 |
p. 3595-3602
8 p.
|
artikel
|
| 16 |
Inhibitors of histone demethylases
|
Lohse, Brian
|
|
2011
|
19 |
12 |
p. 3625-3636
12 p.
|
artikel
|
| 17 |
Modulation of the activity of histone acetyltransferases by long chain alkylidenemalonates (LoCAMs)
|
Milite, Ciro
|
|
2011
|
19 |
12 |
p. 3690-3701
12 p.
|
artikel
|
| 18 |
New FAAH inhibitors based on 3-carboxamido-5-aryl-isoxazole scaffold that protect against experimental colitis
|
Andrzejak, Virginie
|
|
2011
|
19 |
12 |
p. 3777-3786
10 p.
|
artikel
|
| 19 |
Preliminary evaluation of a 3H imidazoquinoline library as dual TLR7/TLR8 antagonists
|
Shukla, Nikunj M.
|
|
2011
|
19 |
12 |
p. 3801-3811
11 p.
|
artikel
|
| 20 |
Selective bone targeting 5-fluorouracil prodrugs: Synthesis and preliminary biological evaluation
|
Ouyang, Liang
|
|
2011
|
19 |
12 |
p. 3750-3756
7 p.
|
artikel
|
| 21 |
Self-assembly pathways of E22Δ-type amyloid β peptide mutants generated from non-aggregative O-acyl isopeptide precursors
|
Sohma, Youhei
|
|
2011
|
19 |
12 |
p. 3787-3792
6 p.
|
artikel
|
| 22 |
Significant enhancement in radical-scavenging activity of curcuminoids conferred by acetoxy substituent at the central methylene carbon
|
Kim, Mi Kyoung
|
|
2011
|
19 |
12 |
p. 3793-3800
8 p.
|
artikel
|
| 23 |
Simplification of the tetracyclic SIRT1-selective inhibitor MC2141: Coumarin- and pyrimidine-based SIRT1/2 inhibitors with different selectivity profile
|
Rotili, Dante
|
|
2011
|
19 |
12 |
p. 3659-3668
10 p.
|
artikel
|
| 24 |
Syntheses of cellotriose and cellotetraose analogues as transition state mimics for mechanistic studies of cellulases
|
Noguchi, Shogo
|
|
2011
|
19 |
12 |
p. 3812-3830
19 p.
|
artikel
|
| 25 |
Synthesis and biological activity of optically active NCL-1, a lysine-specific demethylase 1 selective inhibitor
|
Ogasawara, Daisuke
|
|
2011
|
19 |
12 |
p. 3702-3708
7 p.
|
artikel
|
| 26 |
Synthesis and biological activity of splitomicin analogs targeted at human NAD+-dependent histone deacetylases (sirtuins)
|
Freitag, Marcus
|
|
2011
|
19 |
12 |
p. 3669-3677
9 p.
|
artikel
|
| 27 |
Synthesis and biological testing of novel pyridoisothiazolones as histone acetyltransferase inhibitors
|
Furdas, Silviya D.
|
|
2011
|
19 |
12 |
p. 3678-3689
12 p.
|
artikel
|
| 28 |
Synthesis, structure–affinity relationships, and molecular modeling studies of novel pyrazolo[3,4-c]quinoline derivatives as adenosine receptor antagonists
|
Lenzi, Ombretta
|
|
2011
|
19 |
12 |
p. 3757-3768
12 p.
|
artikel
|
| 29 |
Total synthesis of largazole and analogues: HDAC inhibition, antiproliferative activity and metabolic stability
|
Benelkebir, Hanae
|
|
2011
|
19 |
12 |
p. 3650-3658
9 p.
|
artikel
|
Tijdschrift beschrijving