| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Absolute structures and bioactivities of euryspongins and eurydiene obtained from the marine sponge Euryspongia sp. collected at Iriomote Island
|
Yamazaki, Hiroyuki
|
|
2015
|
23 |
4 |
p. 797-802
6 p.
|
artikel
|
| 2 |
2-Aminophenanthroline dimer stabilized the C–C mismatched duplex DNA
|
Li, Jinxing
|
|
2015
|
23 |
4 |
p. 753-758
6 p.
|
artikel
|
| 3 |
Cytotoxic acyl amides from the soil fungus Gymnascella dankaliensis
|
Hammerschmidt, Lena
|
|
2015
|
23 |
4 |
p. 712-719
8 p.
|
artikel
|
| 4 |
Design and synthesis of new bioisosteres of spirooxindoles (MI-63/219) as anti-breast cancer agents
|
Kumar, Atul
|
|
2015
|
23 |
4 |
p. 839-848
10 p.
|
artikel
|
| 5 |
Design and synthesis of N-methylpyrimidone derivatives as HIV-1 integrase inhibitors
|
Wang, Yujie
|
|
2015
|
23 |
4 |
p. 735-741
7 p.
|
artikel
|
| 6 |
Development of 1,3-diphenyladamantane derivatives as nonsteroidal progesterone receptor antagonists
|
Mori, Shuichi
|
|
2015
|
23 |
4 |
p. 803-809
7 p.
|
artikel
|
| 7 |
Development of potent dopamine–norepinephrine uptake inhibitors (DNRIs) based on a (2S,4R,5R)-2-benzhydryl-5-((4-methoxybenzyl)amino)tetrahydro-2H-pyran-4-ol molecular template
|
Santra, Soumava
|
|
2015
|
23 |
4 |
p. 821-828
8 p.
|
artikel
|
| 8 |
Discovery of 3H-imidazo[4,5-c]quinolin-4(5H)-ones as potent and selective dipeptidyl peptidase IV (DPP-4) inhibitors: Use of a carboxylate prodrug to improve bioavailability
|
Ikuma, Yohei
|
|
2015
|
23 |
4 |
p. 779-790
12 p.
|
artikel
|
| 9 |
Discovery of novel Bruton’s tyrosine kinase (BTK) inhibitors bearing a pyrrolo[2,3-d]pyrimidine scaffold
|
Zhao, Xinge
|
|
2015
|
23 |
4 |
p. 891-901
11 p.
|
artikel
|
| 10 |
Discovery of phenoxybutanoic acid derivatives as potent endothelin antagonists with antihypertensive activity
|
Cai, Jin
|
|
2015
|
23 |
4 |
p. 657-667
11 p.
|
artikel
|
| 11 |
Discovery of 1-substituted benzyl-quinazoline-2,4(1H,3H)-dione derivatives as novel poly(ADP-ribose)polymerase-1 inhibitors
|
Yao, Haiping
|
|
2015
|
23 |
4 |
p. 681-693
13 p.
|
artikel
|
| 12 |
Docking model of the nicotinic acetylcholine receptor and nitromethylene neonicotinoid derivatives with a longer chiral substituent and their biological activities
|
Nagaoka, Hikaru
|
|
2015
|
23 |
4 |
p. 759-769
11 p.
|
artikel
|
| 13 |
Editorial board
|
|
|
2015
|
23 |
4 |
p. IFC-
1 p.
|
artikel
|
| 14 |
Furan-based acetylating agent for the chemical modification of proteins
|
De, Sudipta
|
|
2015
|
23 |
4 |
p. 791-796
6 p.
|
artikel
|
| 15 |
Fused-ring structure of decahydroisoquinolin as a novel scaffold for SARS 3CL protease inhibitors
|
Shimamoto, Yasuhiro
|
|
2015
|
23 |
4 |
p. 876-890
15 p.
|
artikel
|
| 16 |
Graphical contents list
|
|
|
2015
|
23 |
4 |
p. 649-656
8 p.
|
artikel
|
| 17 |
Multifunctional scutellarin–rivastigmine hybrids with cholinergic, antioxidant, biometal chelating and neuroprotective properties for the treatment of Alzheimer’s disease
|
Sang, Zhipei
|
|
2015
|
23 |
4 |
p. 668-680
13 p.
|
artikel
|
| 18 |
Novel, potent, orally bioavailable and selective mycobacterial ATP synthase inhibitors that demonstrated activity against both replicating and non-replicating M. tuberculosis
|
Singh, Supriya
|
|
2015
|
23 |
4 |
p. 742-752
11 p.
|
artikel
|
| 19 |
Rational design of specific binding hairpin Py–Im polyamides targeting human telomere sequences
|
Guo, Chuanxin
|
|
2015
|
23 |
4 |
p. 855-860
6 p.
|
artikel
|
| 20 |
Reversible and irreversible small molecule inhibitors of monoamine oxidase B (MAO-B) investigated by biophysical techniques
|
Rojas, Rafael J.
|
|
2015
|
23 |
4 |
p. 770-778
9 p.
|
artikel
|
| 21 |
Saccharin: A lead compound for structure-based drug design of carbonic anhydrase IX inhibitors
|
Mahon, Brian P.
|
|
2015
|
23 |
4 |
p. 849-854
6 p.
|
artikel
|
| 22 |
Structure–activity relationship study of diphenylamine-based estrogen receptor (ER) antagonists
|
Ohta, Kiminori
|
|
2015
|
23 |
4 |
p. 861-867
7 p.
|
artikel
|
| 23 |
Synthesis and anticancer cell potential of steroidal 16,17-seco-16,17a-dinitriles: Identification of a selective inhibitor of hormone-independent breast cancer cells
|
Nikolić, Andrea R.
|
|
2015
|
23 |
4 |
p. 703-711
9 p.
|
artikel
|
| 24 |
Synthesis and anti-hepatitis B virus activity of C4 amide-substituted isosteviol derivatives
|
Huang, Tsurng-Juhn
|
|
2015
|
23 |
4 |
p. 720-728
9 p.
|
artikel
|
| 25 |
Synthesis and biological evaluation of phosphoramidate prodrugs of two analogues of 2-deoxy-d-ribose-1-phosphate directed to the discovery of two carbasugars as new potential anti-HIV leads
|
Hamon, Nadège
|
|
2015
|
23 |
4 |
p. 829-838
10 p.
|
artikel
|
| 26 |
Synthesis and evaluation of a new Rhodamine B and Di(2-picolyl)amine conjugate as a highly sensitive and selective chemosensor for Al3+ and its application in living-cell imaging
|
Bao, Xiaofeng
|
|
2015
|
23 |
4 |
p. 694-702
9 p.
|
artikel
|
| 27 |
Synthesis and in vitro biological evaluation of 2-(phenylcarbamoyl)phenyl 4-substituted benzoates
|
Krátký, Martin
|
|
2015
|
23 |
4 |
p. 868-875
8 p.
|
artikel
|
| 28 |
Synthesis, biological evaluation and docking analysis of a new series of methylsulfonyl and sulfamoyl acetamides and ethyl acetates as potent COX-2 inhibitors
|
Consalvi, Sara
|
|
2015
|
23 |
4 |
p. 810-820
11 p.
|
artikel
|
| 29 |
Synthesis of 6-[11C]methyl-m-tyrosine ([11C]6MemTyr) for dopamine synthesis imaging in living brain using PET
|
Kanazawa, Masakatsu
|
|
2015
|
23 |
4 |
p. 729-734
6 p.
|
artikel
|
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