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                             19 results found
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
                             19 results found
 
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