| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A collection of caged compounds for probing roles of local translation in neurobiology
|
Sadovski, Oleg
|
|
2010
|
18 |
22 |
p. 7746-7752
7 p.
|
artikel
|
| 2 |
Anticonvulsant activity of 2,4(1H)-diarylimidazoles in mice and rats acute seizure models
|
Zuliani, Valentina
|
|
2010
|
18 |
22 |
p. 7957-7965
9 p.
|
artikel
|
| 3 |
Anti-leishmanial and anti-trypanosomal activities of 1,4-dihydropyridines: In vitro evaluation and structure–activity relationship study
|
Reimão, Juliana Q.
|
|
2010
|
18 |
22 |
p. 8044-8053
10 p.
|
artikel
|
| 4 |
BACE1 inhibitory activities of enantiomerically pure, variously substituted N-(3-(4-benzhydrylpiperazin-1-yl)-2-hydroxypropyl) arylsulfonamides
|
Bertini, Simone
|
|
2010
|
18 |
22 |
p. 7991-7996
6 p.
|
artikel
|
| 5 |
Biflavonoids from Torreya nucifera displaying SARS-CoV 3CLpro inhibition
|
Ryu, Young Bae
|
|
2010
|
18 |
22 |
p. 7940-7947
8 p.
|
artikel
|
| 6 |
Bioengineering functional copolymers. XIV. Synthesis and interaction of poly(N-isopropylacrylamide-co-3,4-dihydro-2H-pyran-alt-maleic anhydride)s with SCLC cancer cells
|
Türk, Mustafa
|
|
2010
|
18 |
22 |
p. 7975-7984
10 p.
|
artikel
|
| 7 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2010
|
18 |
22 |
p. I-III
nvt p.
|
artikel
|
| 8 |
1-Bromo-3-(1′,1′-dimethylalkyl)-1-deoxy-Δ8-tetrahydrocannabinols: New selective ligands for the cannabinoid CB2 receptor
|
Huffman, John W.
|
|
2010
|
18 |
22 |
p. 7809-7815
7 p.
|
artikel
|
| 9 |
Chemical Neurobiology—Introduction
|
Trauner, Dirk
|
|
2010
|
18 |
22 |
p. 7715-
1 p.
|
artikel
|
| 10 |
Conformationally constrained NR2B selective NMDA receptor antagonists derived from ifenprodil: Synthesis and biological evaluation of tetrahydro-3-benzazepine-1,7-diols
|
Tewes, Bastian
|
|
2010
|
18 |
22 |
p. 8005-8015
11 p.
|
artikel
|
| 11 |
Design, syntheses and 3D-QSAR studies of novel N-phenyl pyrrolidin-2-ones and N-phenyl-1H-pyrrol-2-ones as protoporphyrinogen oxidase inhibitors
|
Zhang, Li
|
|
2010
|
18 |
22 |
p. 7948-7956
9 p.
|
artikel
|
| 12 |
Design, synthesis and bioevaluation of dihydropyrazolo[3,4-b]pyridine and benzo[4,5]imidazo[1,2-a]pyrimidine compounds as dual KSP and Aurora-A kinase inhibitors for anti-cancer agents
|
Fu, Rong-geng
|
|
2010
|
18 |
22 |
p. 8035-8043
9 p.
|
artikel
|
| 13 |
Discovery and biological evaluation of potent, selective, orally bioavailable, pyrazine-based blockers of the Nav1.8 sodium channel with efficacy in a model of neuropathic pain
|
Scanio, Marc J.C.
|
|
2010
|
18 |
22 |
p. 7816-7825
10 p.
|
artikel
|
| 14 |
Discovery and synthesis of novel luteolin derivatives as DAT agonists
|
Zhang, Jiange
|
|
2010
|
18 |
22 |
p. 7842-7848
7 p.
|
artikel
|
| 15 |
Editorial board
|
|
|
2010
|
18 |
22 |
p. IFC-
1 p.
|
artikel
|
| 16 |
Evaluation of [11C]metergoline as a PET radiotracer for 5HTR in nonhuman primates
|
Hooker, Jacob M.
|
|
2010
|
18 |
22 |
p. 7739-7745
7 p.
|
artikel
|
| 17 |
Graphical contents list
|
|
|
2010
|
18 |
22 |
p. 7701-7714
14 p.
|
artikel
|
| 18 |
Halogenation of 4-hydroxy/amino-3-methoxyphenyl acetamide TRPV1 agonists showed enhanced antagonism to capsaicin
|
Kang, Dong Wook
|
|
2010
|
18 |
22 |
p. 8092-8105
14 p.
|
artikel
|
| 19 |
Identification by high-throughput screening of inhibitors of Schistosoma mansoni NAD+ catabolizing enzyme
|
Kuhn, Isabelle
|
|
2010
|
18 |
22 |
p. 7900-7910
11 p.
|
artikel
|
| 20 |
Identification of a novel pyrrole derivative endowed with antimycobacterial activity and protection index comparable to that of the current antitubercular drugs streptomycin and rifampin
|
Biava, Mariangela
|
|
2010
|
18 |
22 |
p. 8076-8084
9 p.
|
artikel
|
| 21 |
Indeno[1,2-c]isoquinolin-5,11-diones conjugated to amino acids: Synthesis, cytotoxicity, DNA interaction, and topoisomerase II inhibition properties
|
Ahn, Gang
|
|
2010
|
18 |
22 |
p. 8119-8133
15 p.
|
artikel
|
| 22 |
Inhibition of Helicobacter pylori aminoacyl-tRNA amidotransferase by chloramphenicol analogs
|
Balg, Christian
|
|
2010
|
18 |
22 |
p. 7868-7872
5 p.
|
artikel
|
| 23 |
Intramolecular reductive cyclization strategy to the synthesis of (−)-6-methyl-3-hydroxy-piperidine-2-carboxylic acid, (+)-6-methyl-(2-hydroxymethyl)-piperidine-3-ol and their glycosidase inhibitory activity
|
Pawar, Vishwas U.
|
|
2010
|
18 |
22 |
p. 7799-7803
5 p.
|
artikel
|
| 24 |
In vitro lectin-mediated selection and characterization of rHuEPO-α-binding ssDNA aptamers
|
Zhang, Zhaoyang
|
|
2010
|
18 |
22 |
p. 8016-8025
10 p.
|
artikel
|
| 25 |
Ligand-based virtual screening and ADME-tox guided approach to identify triazolo-quinoxalines as folate cycle inhibitors
|
Carosati, Emanuele
|
|
2010
|
18 |
22 |
p. 7773-7785
13 p.
|
artikel
|
| 26 |
Molecular modeling study on potent and selective adenosine A3 receptor agonists
|
Dal Ben, Diego
|
|
2010
|
18 |
22 |
p. 7923-7930
8 p.
|
artikel
|
| 27 |
Naphthylchalcones induce apoptosis and caspase activation in a leukemia cell line: The relationship between mitochondrial damage, oxidative stress, and cell death
|
Winter, Evelyn
|
|
2010
|
18 |
22 |
p. 8026-8034
9 p.
|
artikel
|
| 28 |
Parallel synthesis and nucleic acid binding properties of C(6′)-α-functionalized bicyclo-DNA
|
Šilhár, Peter
|
|
2010
|
18 |
22 |
p. 7786-7793
8 p.
|
artikel
|
| 29 |
Pharmacology of ionotropic glutamate receptors: A structural perspective
|
Stawski, Philipp
|
|
2010
|
18 |
22 |
p. 7759-7772
14 p.
|
artikel
|
| 30 |
4-Phenylcoumarins from Mesua elegans with acetylcholinesterase inhibitory activity
|
Awang, Khalijah
|
|
2010
|
18 |
22 |
p. 7873-7877
5 p.
|
artikel
|
| 31 |
Pro-apoptotic activity of lipidic α-amino acids isolated from Protopalythoa variabilis
|
Wilke, Diego Veras
|
|
2010
|
18 |
22 |
p. 7997-8004
8 p.
|
artikel
|
| 32 |
Probing the active-site requirements of human intestinal N-terminal maltase-glucoamylase: Synthesis and enzyme inhibitory activities of a six-membered ring nitrogen analogue of kotalanol and its de-O-sulfonated derivative
|
Mohan, Sankar
|
|
2010
|
18 |
22 |
p. 7794-7798
5 p.
|
artikel
|
| 33 |
Pyrazolo[1′,5′:1,6]pyrimido[4,5-d]pyridazin-4(3H)-ones as selective human A1 adenosine receptor ligands
|
Giovannoni, Maria Paola
|
|
2010
|
18 |
22 |
p. 7890-7899
10 p.
|
artikel
|
| 34 |
Redox-silent tocotrienol esters as breast cancer proliferation and migration inhibitors
|
Behery, Fathy A.
|
|
2010
|
18 |
22 |
p. 8066-8075
10 p.
|
artikel
|
| 35 |
Selective accumulation of a novel antimalarial rhodacyanine derivative, SSJ-127, in an organelle of Plasmodium berghei
|
Ikegami-Kawai, Mayumi
|
|
2010
|
18 |
22 |
p. 7804-7808
5 p.
|
artikel
|
| 36 |
Structural and functional characterization of a synthetically modified OmpG
|
Grosse, Wolfgang
|
|
2010
|
18 |
22 |
p. 7716-7723
8 p.
|
artikel
|
| 37 |
Structural insights into the hot spot amino acid residues of mushroom tyrosinase for the bindings of thujaplicins
|
Takahashi, Satoshi
|
|
2010
|
18 |
22 |
p. 8112-8118
7 p.
|
artikel
|
| 38 |
Structure–activity relationships for inhibition of inosine monophosphate dehydrogenase and differentiation induction of K562 cells among the mycophenolic acid derivatives
|
Mitsuhashi, Shinya
|
|
2010
|
18 |
22 |
p. 8106-8111
6 p.
|
artikel
|
| 39 |
Structure–activity relationships of benzimidazole-based selective inhibitors of the mitogen activated kinase-5 signaling pathway
|
Flaherty, Patrick T.
|
|
2010
|
18 |
22 |
p. 8054-8060
7 p.
|
artikel
|
| 40 |
Studies toward the structural optimization of novel thiazolylhydrazone-based potent antitrypanosomal agents
|
Hernandes, Marcelo Zaldini
|
|
2010
|
18 |
22 |
p. 7826-7835
10 p.
|
artikel
|
| 41 |
Synthesis and anticancer activity of new 1-[(5 or 6-substituted 2-alkoxyquinoxalin-3-yl)aminocarbonyl]-4-(hetero)arylpiperazine derivatives
|
Lee, Young Bok
|
|
2010
|
18 |
22 |
p. 7966-7974
9 p.
|
artikel
|
| 42 |
Synthesis and antimalarial activities of rhenium bioorganometallics based on the 4-aminoquinoline structure
|
Arancibia, Rodrigo
|
|
2010
|
18 |
22 |
p. 8085-8091
7 p.
|
artikel
|
| 43 |
Synthesis and antioxidant properties of pulvinic acids analogues
|
Nadal, Brice
|
|
2010
|
18 |
22 |
p. 7931-7939
9 p.
|
artikel
|
| 44 |
Synthesis and evaluation of 2′-O-allyl substituted dinucleotide cap analog for mRNA translation
|
Kore, Anilkumar R.
|
|
2010
|
18 |
22 |
p. 8061-8065
5 p.
|
artikel
|
| 45 |
Synthesis and evaluation of pyrazolone compounds as SARS-coronavirus 3C-like protease inhibitors
|
Ramajayam, R.
|
|
2010
|
18 |
22 |
p. 7849-7854
6 p.
|
artikel
|
| 46 |
Synthesis and evaluation of stilbene derivatives as a potential imaging agent of amyloid plaques
|
Hong, Myeng Chan
|
|
2010
|
18 |
22 |
p. 7724-7730
7 p.
|
artikel
|
| 47 |
Synthesis and evaluation of 5-substituted 9-hydroxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-diones as check point 1 kinase inhibitors
|
Sako, Yuki
|
|
2010
|
18 |
22 |
p. 7878-7889
12 p.
|
artikel
|
| 48 |
Synthesis and SAR studies of chiral non-racemic dexoxadrol analogues as uncompetitive NMDA receptor antagonists
|
Banerjee, Ashutosh
|
|
2010
|
18 |
22 |
p. 7855-7867
13 p.
|
artikel
|
| 49 |
Synthesis, biological evaluation, and molecular docking studies of 2-chloropyridine derivatives possessing 1,3,4-oxadiazole moiety as potential antitumor agents
|
Zheng, Qing-Zhong
|
|
2010
|
18 |
22 |
p. 7836-7841
6 p.
|
artikel
|
| 50 |
Synthesis of new antifungal peptides selective against Cryptococcus neoformans
|
Grimaldi, Manuela
|
|
2010
|
18 |
22 |
p. 7985-7990
6 p.
|
artikel
|
| 51 |
The binding of β-d-glucopyranosyl-thiosemicarbazone derivatives to glycogen phosphorylase: A new class of inhibitors
|
Alexacou, Kyra-Melinda
|
|
2010
|
18 |
22 |
p. 7911-7922
12 p.
|
artikel
|
| 52 |
The GABAA receptor as a target for photochromic molecules
|
Feliciano, Mariel
|
|
2010
|
18 |
22 |
p. 7731-7738
8 p.
|
artikel
|
| 53 |
Two-photon uncaging: New prospects in neuroscience and cellular biology
|
Warther, D.
|
|
2010
|
18 |
22 |
p. 7753-7758
6 p.
|
artikel
|
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