| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel assay revealed that ribonucleotide reductase is functionally important for interstrand DNA crosslink repair
|
Fujii, Naoaki
|
|
2015
|
23 |
21 |
p. 6912-6921
10 p.
|
artikel
|
| 2 |
Antihyperlipidemic morpholine derivatives with antioxidant activity: An investigation of the aromatic substitution
|
Ladopoulou, Eleni M.
|
|
2015
|
23 |
21 |
p. 7015-7023
9 p.
|
artikel
|
| 3 |
Antitumour benzothiazoles. Part 32: DNA adducts and double strand breaks correlate with activity; synthesis of 5F203 hydrogels for local delivery
|
Stone, Erica L.
|
|
2015
|
23 |
21 |
p. 6891-6899
9 p.
|
artikel
|
| 4 |
Antiviral activity of benzotriazole derivatives. 5-[4-(Benzotriazol-2-yl)phenoxy]-2,2-dimethylpentanoic acids potently and selectively inhibit Coxsackie Virus B5
|
Loddo, Roberta
|
|
2015
|
23 |
21 |
p. 7024-7034
11 p.
|
artikel
|
| 5 |
Cleavage of DNA containing 5-fluorocytosine or 5-fluorouracil by type II restriction endonucleases
|
Olszewska, Agata
|
|
2015
|
23 |
21 |
p. 6885-6890
6 p.
|
artikel
|
| 6 |
Click-tailed coumarins with potent and selective inhibitory action against the tumor-associated carbonic anhydrases IX and XII
|
Nocentini, Alessio
|
|
2015
|
23 |
21 |
p. 6955-6966
12 p.
|
artikel
|
| 7 |
Crystal structures of human RIP2 kinase catalytic domain complexed with ATP-competitive inhibitors: Foundations for understanding inhibitor selectivity
|
Charnley, Adam K.
|
|
2015
|
23 |
21 |
p. 7000-7006
7 p.
|
artikel
|
| 8 |
Design of protein homocystamides with enhanced tumor uptake properties for 19F magnetic resonance imaging
|
Chubarov, Alexey S.
|
|
2015
|
23 |
21 |
p. 6943-6954
12 p.
|
artikel
|
| 9 |
Design, synthesis and antibacterial study of new potent and selective coumarin–chalcone derivatives for the treatment of tenacibaculosis
|
Vazquez-Rodriguez, Saleta
|
|
2015
|
23 |
21 |
p. 7045-7052
8 p.
|
artikel
|
| 10 |
Development of novel dipeptide-like rhodesain inhibitors containing the 3-bromoisoxazoline warhead in a constrained conformation
|
Ettari, Roberta
|
|
2015
|
23 |
21 |
p. 7053-7060
8 p.
|
artikel
|
| 11 |
Editorial board
|
|
|
2015
|
23 |
21 |
p. IFC-
1 p.
|
artikel
|
| 12 |
Estrogenic activity of bis(4-hydroxyphenyl)methanes with cyclic hydrophobic structure
|
Kojima, Tomohiro
|
|
2015
|
23 |
21 |
p. 6900-6911
12 p.
|
artikel
|
| 13 |
Evaluation of small molecule SecA inhibitors against methicillin-resistant Staphylococcus aureus
|
Jin, Jinshan
|
|
2015
|
23 |
21 |
p. 7061-7068
8 p.
|
artikel
|
| 14 |
Exploration of labeling by near infrared dyes of the polyproline linker for bivalent-type CXCR4 ligands
|
Nomura, Wataru
|
|
2015
|
23 |
21 |
p. 6967-6973
7 p.
|
artikel
|
| 15 |
Exploration of the linkage elements of porcupine antagonists led to potent Wnt signaling pathway inhibitors
|
Dong, Yan
|
|
2015
|
23 |
21 |
p. 6855-6868
14 p.
|
artikel
|
| 16 |
Graphical contents list
|
|
|
2015
|
23 |
21 |
p. 6775-6783
9 p.
|
artikel
|
| 17 |
Isolation, semisynthesis, covalent docking and transforming growth factor beta-activated kinase 1 (TAK1)-inhibitory activities of (5Z)-7-oxozeaenol analogues
|
Fakhouri, Lara
|
|
2015
|
23 |
21 |
p. 6993-6999
7 p.
|
artikel
|
| 18 |
Isomeric methoxy analogs of nimesulide for development of brain cyclooxygense-2 (COX-2)-targeted imaging agents: Synthesis, in vitro COX-2-inhibitory potency, and cellular transport properties
|
Yamamoto, Yumi
|
|
2015
|
23 |
21 |
p. 6807-6814
8 p.
|
artikel
|
| 19 |
5-Lipoxygenase inhibitors suppress RANKL-induced osteoclast formation via NFATc1 expression
|
Kang, Ju-Hee
|
|
2015
|
23 |
21 |
p. 7069-7078
10 p.
|
artikel
|
| 20 |
New macrocyclic analogs of the natural histone deacetylase inhibitor FK228; design, synthesis and preliminary biological evaluation
|
Ni, Minghong
|
|
2015
|
23 |
21 |
p. 6785-6793
9 p.
|
artikel
|
| 21 |
Novel, potent, selective and cellular active ABC type PTP1B inhibitors containing (methanesulfonyl-phenyl-amino)-acetic acid methyl ester phosphotyrosine mimetic
|
Liu, Peihong
|
|
2015
|
23 |
21 |
p. 7079-7088
10 p.
|
artikel
|
| 22 |
Poly(amidoamine) dendrimers show carbonic anhydrase inhibitory activity against α-, β-, γ- and η-class enzymes
|
Carta, Fabrizio
|
|
2015
|
23 |
21 |
p. 6794-6798
5 p.
|
artikel
|
| 23 |
Ring substitution influences oxidative cyclisation and reactive metabolite formation of nordihydroguaiaretic acid analogues
|
Asiamah, Isaac
|
|
2015
|
23 |
21 |
p. 7007-7014
8 p.
|
artikel
|
| 24 |
Stereospecific inhibition of nitric oxide production in macrophage cells by flavanonols: Synthesis and the structure–activity relationship
|
Jiang, Wen-Jun
|
|
2015
|
23 |
21 |
p. 6922-6929
8 p.
|
artikel
|
| 25 |
Structure activity relationships of benzyl C-region analogs of 2-(3-fluoro-4-methylsulfonamidophenyl)propanamides as potent TRPV1 antagonists
|
Ann, Jihyae
|
|
2015
|
23 |
21 |
p. 6844-6854
11 p.
|
artikel
|
| 26 |
Synthesis and biochemical evaluation of benzoylbenzophenone thiosemicarbazone analogues as potent and selective inhibitors of cathepsin L
|
Parker, Erica N.
|
|
2015
|
23 |
21 |
p. 6974-6992
19 p.
|
artikel
|
| 27 |
Synthesis and biological activity of amino acid derivatives of avarone and its model compound
|
Vilipić, Jovana
|
|
2015
|
23 |
21 |
p. 6930-6942
13 p.
|
artikel
|
| 28 |
Synthesis of fucosylated lacto-N-tetraose using whole-cell biotransformation
|
Baumgärtner, Florian
|
|
2015
|
23 |
21 |
p. 6799-6806
8 p.
|
artikel
|
| 29 |
Synthesis of novel compounds containing morpholine and 5(4H)-oxazolone rings as potent tyrosinase inhibitors
|
Hamidian, Hooshang
|
|
2015
|
23 |
21 |
p. 7089-7094
6 p.
|
artikel
|
| 30 |
Synthesis of scutellarein derivatives to increase biological activity and water solubility
|
Shi, Zhi-Hao
|
|
2015
|
23 |
21 |
p. 6875-6884
10 p.
|
artikel
|
| 31 |
Synthesis of stereochemically diverse cyclic analogs of tubulysins
|
Park, Yunjeong
|
|
2015
|
23 |
21 |
p. 6827-6843
17 p.
|
artikel
|
| 32 |
Synthetic, structural mimetics of the β-hairpin flap of HIV-1 protease inhibit enzyme function
|
Chauhan, Jay
|
|
2015
|
23 |
21 |
p. 7095-7109
15 p.
|
artikel
|
| 33 |
The isolation and synthesis of a novel benzofuran compound from Tephrosia purpurea, and the synthesis of several related derivatives, which suppress histamine H1 receptor gene expression
|
Shill, Manik Chandra
|
|
2015
|
23 |
21 |
p. 6869-6874
6 p.
|
artikel
|
| 34 |
Toward the discovery of dual HCMV–VZV inhibitors: Synthesis, structure activity relationship analysis, and cytotoxicity studies of long chained 2-uracil-3-yl-N-(4-phenoxyphenyl)acetamides
|
Babkov, Denis A.
|
|
2015
|
23 |
21 |
p. 7035-7044
10 p.
|
artikel
|
| 35 |
1,2,3-Triazole-based analogue of benznidazole displays remarkable activity against Trypanosoma cruzi
|
de Andrade, Peterson
|
|
2015
|
23 |
21 |
p. 6815-6826
12 p.
|
artikel
|
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