no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
1 |
Design and discovery of flavonoid-based HIV-1 integrase inhibitors targeting both the active site and the interaction with LEDGF/p75
|
Li, Bo-Wen |
|
2014 |
22 |
12 |
p. 3146-3158 13 p. |
article |
2 |
Design, synthesis and molecular docking of amide and urea derivatives as Escherichia coli PDHc-E1 inhibitors
|
He, Jun-Bo |
|
2014 |
22 |
12 |
p. 3180-3186 7 p. |
article |
3 |
Development of a new class of proteasome inhibitors with an epoxyketone warhead: Rational hybridization of non-peptidic belactosin derivatives and peptide epoxyketones
|
Kawamura, Shuhei |
|
2014 |
22 |
12 |
p. 3091-3095 5 p. |
article |
4 |
Editorial board
|
|
|
2014 |
22 |
12 |
p. IFC- 1 p. |
article |
5 |
Exploring structural motifs necessary for substrate binding in the active site of Escherichia coli pantothenate kinase
|
Awuah, Emelia |
|
2014 |
22 |
12 |
p. 3083-3090 8 p. |
article |
6 |
Graphical contents list
|
|
|
2014 |
22 |
12 |
p. 3067-3071 5 p. |
article |
7 |
Identification of a new selective dopamine D4 receptor ligand
|
Sampson, Dinithia |
|
2014 |
22 |
12 |
p. 3105-3114 10 p. |
article |
8 |
Novel aromatic–polyamine conjugates as cholinesterase inhibitors with notable selectivity toward butyrylcholinesterase
|
Hong, Chen |
|
2014 |
22 |
12 |
p. 3213-3219 7 p. |
article |
9 |
Optimization of diaryl amine derivatives as kinesin spindle protein inhibitors
|
Takeuchi, Tomoki |
|
2014 |
22 |
12 |
p. 3171-3179 9 p. |
article |
10 |
Rational design and synthesis of novel thiazolidin-4-ones as non-nucleoside HIV-1 reverse transcriptase inhibitors
|
Murugesan, Vanangamudi |
|
2014 |
22 |
12 |
p. 3159-3170 12 p. |
article |
11 |
Regulation of responsiveness of phosphorescence toward dissolved oxygen concentration by modulating polymer contents in organic–inorganic hybrid materials
|
Okada, Hiroshi |
|
2014 |
22 |
12 |
p. 3141-3145 5 p. |
article |
12 |
Retinoic acid receptor agonist activity of naturally occurring diterpenes
|
Tanabe, Hiroki |
|
2014 |
22 |
12 |
p. 3204-3212 9 p. |
article |
13 |
Retraction notice to “Carboxylated calixarenes bind strongly to CD69 and protect CD69+ killer cells from suicidal cell death induced by tumor cell surface ligands” [Bioorg. Med. Chem. 18 (4) (2010) 1434–1440]
|
Bezouška, Karel |
|
2014 |
22 |
12 |
p. 3227- 1 p. |
article |
14 |
Structure-guided discovery of 1,3,5 tri-substituted benzenes as potent and selective matriptase inhibitors exhibiting in vivo antitumor efficacy
|
Goswami, Rajeev |
|
2014 |
22 |
12 |
p. 3187-3203 17 p. |
article |
15 |
8-Substituted 2-alkynyl-N 9-propargyladenines as A2A adenosine receptor antagonists
|
Endo, Kazuki |
|
2014 |
22 |
12 |
p. 3072-3082 11 p. |
article |
16 |
Synthesis and biological evaluation of CHX-DAPYs as HIV-1 non-nucleoside reverse transcriptase inhibitors
|
Yan, Zi-Hong |
|
2014 |
22 |
12 |
p. 3220-3226 7 p. |
article |
17 |
Synthesis, biological, and biophysical studies of DAG-indololactones designed as selective activators of RasGRP
|
Garcia, Lia C. |
|
2014 |
22 |
12 |
p. 3123-3140 18 p. |
article |
18 |
Synthesis, biological evaluation and molecular docking studies of trans-indole-3-acrylamide derivatives, a new class of tubulin polymerization inhibitors
|
Baytas, Sultan Nacak |
|
2014 |
22 |
12 |
p. 3096-3104 9 p. |
article |
19 |
The pterocarpanquinone LQB-118 inhibits tumor cell proliferation by downregulation of c-Myc and cyclins D1 and B1 mRNA and upregulation of p21 cell cycle inhibitor expression
|
Martino, Thiago |
|
2014 |
22 |
12 |
p. 3115-3122 8 p. |
article |