| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Benzimidazole inhibitors of the protein kinase CHK2: Clarification of the binding mode by flexible side chain docking and protein–ligand crystallography
|
Matijssen, Cornelis
|
|
2012
|
20 |
22 |
p. 6630-6639
10 p.
|
article
|
| 2 |
Clarifying the structure of granadaene: Total synthesis of related analogue [2]-granadaene and confirmation of its absolute stereochemistry
|
Paradas, Miguel
|
|
2012
|
20 |
22 |
p. 6655-6661
7 p.
|
article
|
| 3 |
Coordination of iron ions in the form of histidinyl dinitrosyl complexes does not prevent their genotoxicity
|
Lewandowska, Hanna
|
|
2012
|
20 |
22 |
p. 6732-6738
7 p.
|
article
|
| 4 |
Design, synthesis, and bioevaluation of benzamides: Novel acetylcholinesterase inhibitors with multi-functions on butylcholinesterase, Aβ aggregation, and β-secretase
|
Peng, Da-Yong
|
|
2012
|
20 |
22 |
p. 6739-6750
12 p.
|
article
|
| 5 |
Dimeric Smac mimetics/IAP inhibitors as in vivo-active pro-apoptotic agents. Part II: Structural and biological characterization
|
Lecis, Daniele
|
|
2012
|
20 |
22 |
p. 6709-6723
15 p.
|
article
|
| 6 |
Effect of adenosine modified with a boron cluster pharmacophore on reactive oxygen species production by human neutrophils
|
Bednarska, Katarzyna
|
|
2012
|
20 |
22 |
p. 6621-6629
9 p.
|
article
|
| 7 |
Exploration of natural compounds as sources of new bifunctional scaffolds targeting cholinesterases and beta amyloid aggregation: The case of chelerythrine
|
Brunhofer, Gerda
|
|
2012
|
20 |
22 |
p. 6669-6679
11 p.
|
article
|
| 8 |
Graphical contents list
|
|
|
2012
|
20 |
22 |
p. 6545-6551
7 p.
|
article
|
| 9 |
Homo- and heterodimeric Smac mimetics/IAP inhibitors as in vivo-active pro-apoptotic agents. Part I: Synthesis
|
Manzoni, Leonardo
|
|
2012
|
20 |
22 |
p. 6687-6708
22 p.
|
article
|
| 10 |
Identification of a novel Smoothened antagonist that potently suppresses Hedgehog signaling
|
Wang, Jiangbo
|
|
2012
|
20 |
22 |
p. 6751-6757
7 p.
|
article
|
| 11 |
4-Isoxazolyl-1,4-dihydropyridines exhibit binding at the multidrug-resistance transporter
|
Hulubei, Victoria
|
|
2012
|
20 |
22 |
p. 6613-6620
8 p.
|
article
|
| 12 |
Molybdophyllysin, a toxic metalloendopeptidase from the tropical toadstool, Chlorophyllum molybdites
|
Yamada, Mina
|
|
2012
|
20 |
22 |
p. 6583-6588
6 p.
|
article
|
| 13 |
Rapid biochemical synthesis of 11C-labeled single chain variable fragment antibody for immuno-PET by cell-free protein synthesis
|
Matsuda, Takayoshi
|
|
2012
|
20 |
22 |
p. 6579-6582
4 p.
|
article
|
| 14 |
SAR studies of epoxycurcuphenol derivatives on leukemia CT-CD4 cells
|
Galindo, José L.G.
|
|
2012
|
20 |
22 |
p. 6662-6668
7 p.
|
article
|
| 15 |
Structure–activity relationship studies of 4-benzyl-1H-pyrazol-3-yl β-d-glucopyranoside derivatives as potent and selective sodium glucose co-transporter 1 (SGLT1) inhibitors with therapeutic activity on postprandial hyperglycemia
|
Fushimi, Nobuhiko
|
|
2012
|
20 |
22 |
p. 6598-6612
15 p.
|
article
|
| 16 |
Sulfonates-PMMA nanoparticles conjugates: A versatile system for multimodal application
|
Monasterolo, Claudio
|
|
2012
|
20 |
22 |
p. 6640-6647
8 p.
|
article
|
| 17 |
Synthesis and evaluation of apoptosis induction of thienopyrimidine compounds on KRAS and BRAF mutated colorectal cancer cell lines
|
Pédeboscq, Stéphane
|
|
2012
|
20 |
22 |
p. 6724-6731
8 p.
|
article
|
| 18 |
Synthesis and structure–activity relationship of berberine analogues in LDLR up-regulation and AMPK activation
|
Wang, Yan-Xiang
|
|
2012
|
20 |
22 |
p. 6552-6558
7 p.
|
article
|
| 19 |
Synthesis and structure–activity relationships of 8-substituted-2-aryl-5-alkylaminoquinolines: Potent, orally active corticotropin-releasing factor-1 receptor antagonists
|
Takeda, Kunitoshi
|
|
2012
|
20 |
22 |
p. 6559-6578
20 p.
|
article
|
| 20 |
Synthesis, biological evaluation and molecular modeling of dihydro-pyrazolyl-thiazolinone derivatives as potential COX-2 inhibitors
|
Qiu, Ke-Ming
|
|
2012
|
20 |
22 |
p. 6648-6654
7 p.
|
article
|
| 21 |
Synthesis of new antimicrobial pyrrolo[2,1-a]isoquinolin-3-ones
|
Moreno, Laura
|
|
2012
|
20 |
22 |
p. 6589-6597
9 p.
|
article
|
| 22 |
Targeting conserved water molecules: Design of 4-aryl-5-cyanopyrrolo[2,3-d]pyrimidine Hsp90 inhibitors using fragment-based screening and structure-based optimization
|
Davies, Nicholas G.M.
|
|
2012
|
20 |
22 |
p. 6770-6789
20 p.
|
article
|
| 23 |
The synthesis and antituberculosis activity of 5′-nor carbocyclic uracil derivatives
|
Matyugina, Elena
|
|
2012
|
20 |
22 |
p. 6680-6686
7 p.
|
article
|
| 24 |
Trimeric purine nucleoside phosphorylase: Exploring postulated one-third-of-the-sites binding in the transition state
|
Wielgus-Kutrowska, Beata
|
|
2012
|
20 |
22 |
p. 6758-6769
12 p.
|
article
|
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