| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A new potential approach to block HIV-1 replication via protein–protein interaction and strand-transfer inhibition
|
Ferro, Stefania
|
|
2014
|
22 |
7 |
p. 2269-2279
11 p.
|
artikel
|
| 2 |
Antiproliferative activities of halogenated thieno[3,2-d]pyrimidines
|
Temburnikar, Kartik W.
|
|
2014
|
22 |
7 |
p. 2113-2122
10 p.
|
artikel
|
| 3 |
Application of encoded library technology (ELT) to a protein–protein interaction target: Discovery of a potent class of integrin lymphocyte function-associated antigen 1 (LFA-1) antagonists
|
Kollmann, Christopher S.
|
|
2014
|
22 |
7 |
p. 2353-2365
13 p.
|
artikel
|
| 4 |
Benzophenone C-glucosides and gallotannins from mango tree stem bark with broad-spectrum anti-viral activity
|
Abdel-Mageed, Wael M.
|
|
2014
|
22 |
7 |
p. 2236-2243
8 p.
|
artikel
|
| 5 |
Binding free energies for nicotine analogs inhibiting cytochrome P450 2A6 by a combined use of molecular dynamics simulations and QM/MM-PBSA calculations
|
Lu, Haiting
|
|
2014
|
22 |
7 |
p. 2149-2156
8 p.
|
artikel
|
| 6 |
Camphor-based symmetric diimines as inhibitors of influenza virus reproduction
|
Sokolova, Anastasiya S.
|
|
2014
|
22 |
7 |
p. 2141-2148
8 p.
|
artikel
|
| 7 |
Characterization of the four isomers of 123I-CMICE-013: A potential SPECT myocardial perfusion imaging agent
|
Wei, Lihui
|
|
2014
|
22 |
7 |
p. 2033-2044
12 p.
|
artikel
|
| 8 |
Chemically defined polyethylene glycol siRNA conjugates with enhanced gene silencing effect
|
Gaziova, Zuzana
|
|
2014
|
22 |
7 |
p. 2320-2326
7 p.
|
artikel
|
| 9 |
Computer-aided identification of novel 3,5-substituted rhodanine derivatives with activity against Staphylococcus aureus DNA gyrase
|
Werner, Malela M.
|
|
2014
|
22 |
7 |
p. 2176-2187
12 p.
|
artikel
|
| 10 |
Corrigendum to “Design, structure–activity relationship, and highly efficient asymmetric synthesis of 3-phenyl-4-benzylaminopiperidine derivatives as novel neurokinin-1 receptor antagonists” [Bioorg. Med. Chem. 19 (2011) 6430–6446]
|
Shirai, Junya
|
|
2014
|
22 |
7 |
p. 2379-
1 p.
|
artikel
|
| 11 |
Decreasing acidity in a series of aldose reductase inhibitors: 2-Fluoro-4-(1H-pyrrol-1-yl)phenol as a scaffold for improved membrane permeation
|
Chatzopoulou, Maria
|
|
2014
|
22 |
7 |
p. 2194-2207
14 p.
|
artikel
|
| 12 |
Design and synthesis of conformationally restricted inhibitors of active thrombin activatable fibrinolysis inhibitor (TAFIa)
|
Brink, Mikael
|
|
2014
|
22 |
7 |
p. 2261-2268
8 p.
|
artikel
|
| 13 |
Design and synthesis of silicon-containing steroid sulfatase inhibitors possessing pro-estrogen antagonistic character
|
Kajita, Daisuke
|
|
2014
|
22 |
7 |
p. 2244-2252
9 p.
|
artikel
|
| 14 |
Design, synthesis and biological evaluation of a series of pyrano chalcone derivatives containing indole moiety as novel anti-tubulin agents
|
Wang, Guangcheng
|
|
2014
|
22 |
7 |
p. 2060-2079
20 p.
|
artikel
|
| 15 |
Design, synthesis and biological evaluation of new 5-nitro benzimidazole derivatives as AT1 antagonists with anti-hypertension activities
|
Zhu, Weibo
|
|
2014
|
22 |
7 |
p. 2294-2302
9 p.
|
artikel
|
| 16 |
Design, synthesis and biological evaluation of novel 6-alkenylamides substituted of 4-anilinothieno[2,3-d]pyrimidines as irreversible epidermal growth factor receptor inhibitors
|
Ji, Xun
|
|
2014
|
22 |
7 |
p. 2366-2378
13 p.
|
artikel
|
| 17 |
Discovery of 3-(4-methanesulfonylphenoxy)-N-[1-(2-methoxy-ethoxymethyl)-1H-pyrazol-3-yl]-5-(3-methylpyridin-2-yl)-benzamide as a novel glucokinase activator (GKA) for the treatment of type 2 diabetes mellitus
|
Park, Kaapjoo
|
|
2014
|
22 |
7 |
p. 2280-2293
14 p.
|
artikel
|
| 18 |
[Dmt1]DALDA analogues with enhanced μ opioid agonist potency and with a mixed μ/κ opioid activity profile
|
Bai, Longxiang
|
|
2014
|
22 |
7 |
p. 2333-2338
6 p.
|
artikel
|
| 19 |
Editorial board
|
|
|
2014
|
22 |
7 |
p. IFC-
1 p.
|
artikel
|
| 20 |
Endomorphin analogues with mixed μ-opioid (MOP) receptor agonism/δ-opioid (DOP) receptor antagonism and lacking β-arrestin2 recruitment activity
|
Cai, Jun
|
|
2014
|
22 |
7 |
p. 2208-2219
12 p.
|
artikel
|
| 21 |
Expanded potential of seleno-carbohydrates as a molecular tool for X-ray structural determination of a carbohydrate–protein complex with single/multi-wavelength anomalous dispersion phasing
|
Suzuki, Tatsuya
|
|
2014
|
22 |
7 |
p. 2090-2101
12 p.
|
artikel
|
| 22 |
Facile synthesis, cytotoxicity and bioimaging of Fe3+ selective fluorescent chemosensor
|
Saleem, Muhammad
|
|
2014
|
22 |
7 |
p. 2045-2051
7 p.
|
artikel
|
| 23 |
Fused heterocyclic compounds bearing bridgehead nitrogen as potent HIV-1 NNRTIs. Part 1: Design, synthesis and biological evaluation of novel 5,7-disubstituted pyrazolo[1,5-a]pyrimidine derivatives
|
Tian, Ye
|
|
2014
|
22 |
7 |
p. 2052-2059
8 p.
|
artikel
|
| 24 |
Graphical contents list
|
|
|
2014
|
22 |
7 |
p. 1973-1982
10 p.
|
artikel
|
| 25 |
N-Acyl-phosphoramidates as potential novel form of gemcitabine prodrugs
|
Baraniak, Janina
|
|
2014
|
22 |
7 |
p. 2133-2140
8 p.
|
artikel
|
| 26 |
Novel nitroimidazole alkylsulfonamides as hypoxic cell radiosensitisers
|
Bonnet, Muriel
|
|
2014
|
22 |
7 |
p. 2123-2132
10 p.
|
artikel
|
| 27 |
Pyrrolopyrimidine-inhibitors with hydantoin moiety as spacer can explore P4/S4 interaction on plasmin
|
Teno, Naoki
|
|
2014
|
22 |
7 |
p. 2339-2352
14 p.
|
artikel
|
| 28 |
Recognition of RNA duplex by a neomycin–Hoechst 33258 conjugate
|
Willis, Bert
|
|
2014
|
22 |
7 |
p. 2327-2332
6 p.
|
artikel
|
| 29 |
Some non-conventional biomolecular targets for diamidines. A short survey
|
Huang, Tien L.
|
|
2014
|
22 |
7 |
p. 1983-1992
10 p.
|
artikel
|
| 30 |
Studies on the antiproliferative effects of tropolone derivatives in Jurkat T-lymphocyte cells
|
Ononye, Sophia N.
|
|
2014
|
22 |
7 |
p. 2188-2193
6 p.
|
artikel
|
| 31 |
Synthesis and anticonvulsant activity of some new pyrazolo[3,4-b]pyrazines and related heterocycles
|
Farghaly, Abdel-Rahman
|
|
2014
|
22 |
7 |
p. 2166-2175
10 p.
|
artikel
|
| 32 |
Synthesis and biological evaluation of new pyrazolone–pyridazine conjugates as anti-inflammatory and analgesic agents
|
Khalil, Nadia Abdalla
|
|
2014
|
22 |
7 |
p. 2080-2089
10 p.
|
artikel
|
| 33 |
Synthesis and evaluation of effective photoaffinity probe molecule of furospinosulin-1, a hypoxia-selective growth inhibitor
|
Kotoku, Naoyuki
|
|
2014
|
22 |
7 |
p. 2102-2112
11 p.
|
artikel
|
| 34 |
Synthesis and methemoglobinemia-inducing properties of benzocaine isosteres designed as humane rodenticides
|
Conole, Daniel
|
|
2014
|
22 |
7 |
p. 2220-2235
16 p.
|
artikel
|
| 35 |
Synthesis, biological evaluation and 3D-QSAR studies of new chalcone derivatives as inhibitors of human P-glycoprotein
|
Parveen, Zahida
|
|
2014
|
22 |
7 |
p. 2311-2319
9 p.
|
artikel
|
| 36 |
Synthetic approaches to the 2012 new drugs
|
Ding, Hong X.
|
|
2014
|
22 |
7 |
p. 2005-2032
28 p.
|
artikel
|
| 37 |
The chemistry and biology of febrifugine and halofuginone
|
McLaughlin, Noel P.
|
|
2014
|
22 |
7 |
p. 1993-2004
12 p.
|
artikel
|
| 38 |
The identification, analysis and structure-based development of novel inhibitors of 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase
|
Yun, Mi-Kyung
|
|
2014
|
22 |
7 |
p. 2157-2165
9 p.
|
artikel
|
| 39 |
The identification of novel 5′-amino gemcitabine analogs as potent RRM1 inhibitors
|
Labroli, Marc A.
|
|
2014
|
22 |
7 |
p. 2303-2310
8 p.
|
artikel
|
| 40 |
Using ‘biased-privileged’ scaffolds to identify lysine methyltransferase inhibitors
|
Kashyap, Sudhir
|
|
2014
|
22 |
7 |
p. 2253-2260
8 p.
|
artikel
|
Tijdschrift beschrijving