| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Analogue-based design, synthesis and docking of non-steroidal anti-inflammatory agents. Part 2: Methyl sulfanyl/methyl sulfonyl substituted 2,3-diaryl-2,3-dihydro-1H-quinazolin-4-ones
|
Manivannan, E.
|
|
2012
|
20 |
24 |
p. 7119-7127
9 p.
|
artikel
|
| 2 |
Anti-infective and herbicidal activity of N-substituted 2-aminobenzothiazoles
|
Fajkusova, Dagmar
|
|
2012
|
20 |
24 |
p. 7059-7068
10 p.
|
artikel
|
| 3 |
A practical post-modification synthesis of oligodeoxynucleotides containing 4,7-diaminoimidazo[5′,4′:4,5]pyrido[2,3-d]pyrimidine nucleoside
|
Tarashima, Noriko
|
|
2012
|
20 |
24 |
p. 7095-7100
6 p.
|
artikel
|
| 4 |
5-(1,3-Benzothiazol-6-yl)-4-(4-methyl-1,3-thiazol-2-yl)-1H-imidazole derivatives as potent and selective transforming growth factor-β type I receptor inhibitors
|
Amada, Hideaki
|
|
2012
|
20 |
24 |
p. 7128-7138
11 p.
|
artikel
|
| 5 |
Bicyclic peptidomimetics targeting secreted aspartic protease 2 (SAP2) from Candida albicans reveal a constrained inhibitory chemotype
|
Calugi, Chiara
|
|
2012
|
20 |
24 |
p. 7206-7213
8 p.
|
artikel
|
| 6 |
Contribution to investigation of antimicrobial activity of styrylquinolines
|
Cieslik, Wioleta
|
|
2012
|
20 |
24 |
p. 6960-6968
9 p.
|
artikel
|
| 7 |
Design, synthesis, and evaluation of imidazo[1,2-b]pyridazine derivatives having a benzamide unit as novel VEGFR2 kinase inhibitors
|
Miyamoto, Naoki
|
|
2012
|
20 |
24 |
p. 7051-7058
8 p.
|
artikel
|
| 8 |
DNA binding acridine–thiazolidinone agents affecting intracellular glutathione
|
Paulíková, Helena
|
|
2012
|
20 |
24 |
p. 7139-7148
10 p.
|
artikel
|
| 9 |
Editorial board
|
|
|
2012
|
20 |
24 |
p. IFC-
1 p.
|
artikel
|
| 10 |
G-quadruplex DNA cleavage preference and identification of a perylene diimide G-quadruplex photocleavage agent using a rapid fluorescent assay
|
Schoonover, Michelle
|
|
2012
|
20 |
24 |
p. 6904-6918
15 p.
|
artikel
|
| 11 |
Graphical contents list
|
|
|
2012
|
20 |
24 |
p. 6895-6903
9 p.
|
artikel
|
| 12 |
Halogenated pentamethine cyanine dyes exhibiting high fidelity for G-quadruplex DNA
|
Nanjunda, Rupesh
|
|
2012
|
20 |
24 |
p. 7002-7011
10 p.
|
artikel
|
| 13 |
Influence of thiostrepton binding on the ribosomal GTPase associated region characterized by molecular dynamics simulation
|
Wolf, Antje
|
|
2012
|
20 |
24 |
p. 7194-7205
12 p.
|
artikel
|
| 14 |
Inhibition of monoamine oxidase by 8-[(phenylethyl)sulfanyl]caffeine analogues
|
Mostert, Samantha
|
|
2012
|
20 |
24 |
p. 7040-7050
11 p.
|
artikel
|
| 15 |
Isolation and synthesis of two antiproliferative calamenene-type sesquiterpenoids from Sterculia tavia from the Madagascar Rain Forest
|
Dai, Yumin
|
|
2012
|
20 |
24 |
p. 6940-6944
5 p.
|
artikel
|
| 16 |
Mannich bases of scutellarein as thrombin-inhibitors: Design, synthesis, biological activity and solubility
|
Li, Nian-Guang
|
|
2012
|
20 |
24 |
p. 6919-6923
5 p.
|
artikel
|
| 17 |
Microwave assisted synthesis and anti-influenza virus activity of 1-adamantyl substituted N-(1-thia-4-azaspiro[4.5]decan-4-yl)carboxamide derivatives
|
Göktaş, Füsun
|
|
2012
|
20 |
24 |
p. 7155-7159
5 p.
|
artikel
|
| 18 |
Novel coumarin derivatives bearing N-benzyl pyridinium moiety: Potent and dual binding site acetylcholinesterase inhibitors
|
Alipour, Masoumeh
|
|
2012
|
20 |
24 |
p. 7214-7222
9 p.
|
artikel
|
| 19 |
N-Phenyl-4-hydroxy-2-quinolone-3-carboxamides as selective inhibitors of mutant H1047R phosphoinositide-3-kinase (PI3Kα)
|
Sabbah, Dima A.
|
|
2012
|
20 |
24 |
p. 7175-7183
9 p.
|
artikel
|
| 20 |
Optimization and structure–activity relationships of a series of potent inhibitors of methicillin-resistant Staphylococcus aureus (MRSA) pyruvate kinase as novel antimicrobial agents
|
Kumar, Nag S.
|
|
2012
|
20 |
24 |
p. 7069-7082
14 p.
|
artikel
|
| 21 |
Optimization of thiazole analogues of resveratrol for induction of NAD(P)H:quinone reductase 1 (QR1)
|
Mayhoub, Abdelrahman S.
|
|
2012
|
20 |
24 |
p. 7030-7039
10 p.
|
artikel
|
| 22 |
3-Phenyl substituted 6,7-dimethoxyisoquinoline derivatives as FtsZ-targeting antibacterial agents
|
Kelley, Cody
|
|
2012
|
20 |
24 |
p. 7012-7029
18 p.
|
artikel
|
| 23 |
Purpuroines A–J, halogenated alkaloids from the sponge Iotrochota purpurea with antibiotic activity and regulation of tyrosine kinases
|
Shen, Shi
|
|
2012
|
20 |
24 |
p. 6924-6928
5 p.
|
artikel
|
| 24 |
SIB-DOTA: A trifunctional prosthetic group potentially amenable for multi-modal labeling that enhances tumor uptake of internalizing monoclonal antibodies
|
Vaidyanathan, G.
|
|
2012
|
20 |
24 |
p. 6929-6939
11 p.
|
artikel
|
| 25 |
Synthesis and antimalarial evaluation of a screening library based on a tetrahydroanthraquinone natural product scaffold
|
Choomuenwai, Vanida
|
|
2012
|
20 |
24 |
p. 7167-7174
8 p.
|
artikel
|
| 26 |
Synthesis and biological evaluation of new fluorine substituted derivatives as angiotensin II receptor antagonists with anti-hypertension and anti-tumor effects
|
Da, Ya-jing
|
|
2012
|
20 |
24 |
p. 7101-7111
11 p.
|
artikel
|
| 27 |
Synthesis and biological evaluation of 2-substituted-4-(3′,4′,5′-trimethoxyphenyl)-5-aryl thiazoles as anticancer agents
|
Romagnoli, Romeo
|
|
2012
|
20 |
24 |
p. 7083-7094
12 p.
|
artikel
|
| 28 |
Synthesis and cytotoxic activities of estrone and estradiol cis-dichloroplatinum(II) complexes
|
Kvasnica, Miroslav
|
|
2012
|
20 |
24 |
p. 6969-6978
10 p.
|
artikel
|
| 29 |
Synthesis and DNA interaction of ethylenediamine platinum(II) complexes linked to DNA intercalants
|
Duskova, Katerina
|
|
2012
|
20 |
24 |
p. 7112-7118
7 p.
|
artikel
|
| 30 |
Synthesis and docking studies of novel antitumor benzimidazoles
|
Omar, Mohamed A.
|
|
2012
|
20 |
24 |
p. 6989-7001
13 p.
|
artikel
|
| 31 |
Synthesis and SAR study of 4,5-diaryl-1H-imidazole-2(3H)-thione derivatives, as potent 15-lipoxygenase inhibitors
|
Assadieskandar, Amir
|
|
2012
|
20 |
24 |
p. 7160-7166
7 p.
|
artikel
|
| 32 |
Synthesis of 6″-triazole-substituted α-GalCer analogues as potent iNKT cell stimulating ligands
|
Pauwels, Nora
|
|
2012
|
20 |
24 |
p. 7149-7154
6 p.
|
artikel
|
| 33 |
The interaction of nemorubicin metabolite PNU-159682 with DNA fragments d(CGTACG)2, d(CGATCG)2 and d(CGCGCG)2 shows a strong but reversible binding to G:C base pairs
|
Mazzini, Stefania
|
|
2012
|
20 |
24 |
p. 6979-6988
10 p.
|
artikel
|
| 34 |
Triazole pyrimidine nucleosides as inhibitors of Ribonuclease A. Synthesis, biochemical, and structural evaluation
|
Parmenopoulou, Vanessa
|
|
2012
|
20 |
24 |
p. 7184-7193
10 p.
|
artikel
|
| 35 |
Virtual screening and QSAR study of some pyrrolidine derivatives as α-mannosidase inhibitors for binding feature analysis
|
Moorthy, N.S.H.N.
|
|
2012
|
20 |
24 |
p. 6945-6959
15 p.
|
artikel
|
Tijdschrift beschrijving