| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acridone-tagged DNA as a new probe for DNA detection by fluorescence resonance energy transfer and for mismatch DNA recognition
|
Hagiwara, Yasuhisa
|
|
2008
|
16 |
14 |
p. 7013-7020
8 p.
|
artikel
|
| 2 |
Affinity of 3-acyl substituted 4-quinolones at the benzodiazepine site of GABAA receptors
|
Lager, Erik
|
|
2008
|
16 |
14 |
p. 6936-6948
13 p.
|
artikel
|
| 3 |
4-(Anilino)pyrrole-2-carboxamides: Novel non-steroidal/non-anilide type androgen antagonists effective upon human prostate tumor LNCaP cells with mutated nuclear androgen receptor
|
Wakabayashi, Ken-ichi
|
|
2008
|
16 |
14 |
p. 6799-6812
14 p.
|
artikel
|
| 4 |
Antileishmanial activity screening of 5-nitro-2-heterocyclic benzylidene hydrazides
|
Rando, Daniela G.
|
|
2008
|
16 |
14 |
p. 6724-6731
8 p.
|
artikel
|
| 5 |
Antiprion activity of functionalized 9-aminoacridines related to quinacrine
|
Nguyen Thi, Hanh Thuy
|
|
2008
|
16 |
14 |
p. 6737-6746
10 p.
|
artikel
|
| 6 |
Anti-retroviral and cytostatic activity of 2′,3′-dideoxyribonucleoside 3′-disulfides
|
Gerland, Béatrice
|
|
2008
|
16 |
14 |
p. 6824-6831
8 p.
|
artikel
|
| 7 |
A re-examination of the difluoromethylenesulfonic acid group as a phosphotyrosine mimic for PTP1B inhibition
|
Hussain, Munawar
|
|
2008
|
16 |
14 |
p. 6764-6777
14 p.
|
artikel
|
| 8 |
BACE1 inhibitory effects of lavandulyl flavanones from Sophora flavescens
|
Hwang, Eun Mi
|
|
2008
|
16 |
14 |
p. 6669-6674
6 p.
|
artikel
|
| 9 |
Carbaporphyrin ketals as potential agents for a new photodynamic therapy treatment of leishmaniasis
|
Morgenthaler, Justin B.
|
|
2008
|
16 |
14 |
p. 7033-7038
6 p.
|
artikel
|
| 10 |
Conjugates of gonadotropin releasing hormone (GnRH) with carminic acid: Synthesis, generation of reactive oxygen species (ROS) and biological evaluation
|
Lev-Goldman, Vered
|
|
2008
|
16 |
14 |
p. 6789-6798
10 p.
|
artikel
|
| 11 |
Corrigendum to “Synthesis and in vitro evaluation of leishmanicidal and trypanocidal activities of N-quinolin-8-yl-arylsulfonamides” [Bioorg. Med. Chem. 15 (2007) 7553–7560]
|
da Silva, Luiz Everson
|
|
2008
|
16 |
14 |
p. 7079-
1 p.
|
artikel
|
| 12 |
Corrigendum to “Synthesis and structure–activity relationships of N-{1-[(6-fluoro-2-naphthyl)methyl]piperidin-4-yl}benzamide derivatives as novel CCR3 antagonists” [Bioorg. Med. Chem. 16 (2008) 144–156]
|
Sato, Ippei
|
|
2008
|
16 |
14 |
p. 7078-
1 p.
|
artikel
|
| 13 |
2-Deoxy-2,3-didehydro-N-acetylneuraminic acid analogs structurally modified by thiocarbamoylalkyl groups at the C-4 position: Synthesis and biological evaluation as inhibitors of human parainfluenza virus type 1
|
Ikeda, Kiyoshi
|
|
2008
|
16 |
14 |
p. 6783-6788
6 p.
|
artikel
|
| 14 |
Design, synthesis, and structure–affinity relationship studies in NK1 receptor ligands based on azole-fused quinolinecarboxamide moieties
|
Cappelli, Andrea
|
|
2008
|
16 |
14 |
p. 6850-6859
10 p.
|
artikel
|
| 15 |
Development of novel β-amyloid probes based on 3,5-diphenyl-1,2,4-oxadiazole
|
Ono, Masahiro
|
|
2008
|
16 |
14 |
p. 6867-6872
6 p.
|
artikel
|
| 16 |
Diarylheptanoids, new phytoestrogens from the rhizomes of Curcuma comosa: Isolation, chemical modification and estrogenic activity evaluation
|
Suksamrarn, Apichart
|
|
2008
|
16 |
14 |
p. 6891-6902
12 p.
|
artikel
|
| 17 |
Discovery and SAR of 2-(1-propylpiperidin-4-yl)-1H-benzimidazole-4-carboxamide: A potent inhibitor of poly(ADP-ribose) polymerase (PARP) for the treatment of cancer
|
Penning, Thomas D.
|
|
2008
|
16 |
14 |
p. 6965-6975
11 p.
|
artikel
|
| 18 |
Discovery of aminoquinolines as a new class of potent inhibitors of heat shock protein 90 (Hsp90): Synthesis, biology, and molecular modeling
|
Ganesh, Thota
|
|
2008
|
16 |
14 |
p. 6903-6910
8 p.
|
artikel
|
| 19 |
Discovery of potent CCR4 antagonists: Synthesis and structure–activity relationship study of 2,4-diaminoquinazolines
|
Yokoyama, Kazuhiro
|
|
2008
|
16 |
14 |
p. 7021-7032
12 p.
|
artikel
|
| 20 |
Editorial board
|
|
|
2008
|
16 |
14 |
p. IFC-
1 p.
|
artikel
|
| 21 |
G-quadruplex structures of human telomere DNA examined by single molecule FRET and BrG-substitution
|
Okamoto, Kenji
|
|
2008
|
16 |
14 |
p. 6873-6879
7 p.
|
artikel
|
| 22 |
Graphical contents list
|
|
|
2008
|
16 |
14 |
p. 6651-6662
12 p.
|
artikel
|
| 23 |
Halicyclamine A, a marine spongean alkaloid as a lead for anti-tuberculosis agent
|
Arai, Masayoshi
|
|
2008
|
16 |
14 |
p. 6732-6736
5 p.
|
artikel
|
| 24 |
Instructions to contributors
|
|
|
2008
|
16 |
14 |
p. I-
1 p.
|
artikel
|
| 25 |
β-Ketophosphonates as β-lactamase inhibitors: Intramolecular cooperativity between the hydrophobic subsites of a class D β-lactamase
|
Perumal, Senthil K.
|
|
2008
|
16 |
14 |
p. 6987-6994
8 p.
|
artikel
|
| 26 |
Ligands to the (IRAP)/AT4 receptor encompassing a 4-hydroxydiphenylmethane scaffold replacing Tyr2
|
Andersson, Hanna
|
|
2008
|
16 |
14 |
p. 6924-6935
12 p.
|
artikel
|
| 27 |
Locking the two ends of tetrapeptidic HTLV-I protease inhibitors inside the enzyme
|
Zhang, Meihui
|
|
2008
|
16 |
14 |
p. 6880-6890
11 p.
|
artikel
|
| 28 |
Mixed tetraoxanes containing the acetone subunit as antimalarials
|
Opsenica, Dejan M.
|
|
2008
|
16 |
14 |
p. 7039-7045
7 p.
|
artikel
|
| 29 |
N-Arylmethyl substituted iminoribitol derivatives as inhibitors of a purine specific nucleoside hydrolase
|
Goeminne, Annelies
|
|
2008
|
16 |
14 |
p. 6752-6763
12 p.
|
artikel
|
| 30 |
New trypanocidal hybrid compounds from the association of hydrazone moieties and benzofuroxan heterocycle
|
Porcal, Williams
|
|
2008
|
16 |
14 |
p. 6995-7004
10 p.
|
artikel
|
| 31 |
2-N-Methyl modifications and SAR studies of manzamine A
|
Ibrahim, Mohamed A.
|
|
2008
|
16 |
14 |
p. 6702-6706
5 p.
|
artikel
|
| 32 |
Novel aminopeptidase N inhibitors derived from 1,3,4-thiadiazole scaffold
|
Tu, GuoGang
|
|
2008
|
16 |
14 |
p. 6663-6668
6 p.
|
artikel
|
| 33 |
Novel amodiaquine congeners as potent antimalarial agents
|
Casagrande, Manolo
|
|
2008
|
16 |
14 |
p. 6813-6823
11 p.
|
artikel
|
| 34 |
Oxidative transformation of 2-acetylaminofluorene by a chemical model for cytochrome P450: A water-insoluble porphyrin and tert-butyl hydroperoxide
|
Inami, Keiko
|
|
2008
|
16 |
14 |
p. 7070-7077
8 p.
|
artikel
|
| 35 |
Progesterone receptor antagonists with a 3-phenylquinazoline-2,4-dione/2-phenylisoquinoline-1,3-dione skeleton
|
Nakagawa, Aya
|
|
2008
|
16 |
14 |
p. 7046-7054
9 p.
|
artikel
|
| 36 |
QSAR modeling of the antifungal activity against Candida albicans for a diverse set of organic compounds
|
Katritzky, Alan R.
|
|
2008
|
16 |
14 |
p. 7055-7069
15 p.
|
artikel
|
| 37 |
Selective angiotensin II AT2 receptor agonists: Benzamide structure–activity relationships
|
Wallinder, Charlotta
|
|
2008
|
16 |
14 |
p. 6841-6849
9 p.
|
artikel
|
| 38 |
Studies toward the discovery of the next generation of antidepressants. Part 6: Dual 5-HT1A receptor and serotonin transporter affinity within a class of arylpiperazinyl-cyclohexyl indole derivatives
|
Zhou, Dahui
|
|
2008
|
16 |
14 |
p. 6707-6723
17 p.
|
artikel
|
| 39 |
Study by HPLC-MS of the interaction of platinum antitumor complexes with potato carboxypeptidase inhibitor (PCI)
|
Martínez, Alberto
|
|
2008
|
16 |
14 |
p. 6832-6840
9 p.
|
artikel
|
| 40 |
Study of chemical stability of antivirally active 5-azacytosine acyclic nucleoside phosphonates using NMR spectroscopy
|
Dračínský, Martin
|
|
2008
|
16 |
14 |
p. 6778-6782
5 p.
|
artikel
|
| 41 |
2-Substituted-16-ene-22-thia-1α,25-dihydroxy-26,27-dimethyl-19-norvitamin D3 analogs: Synthesis, biological evaluation, and crystal structure
|
Shimizu, Masato
|
|
2008
|
16 |
14 |
p. 6949-6964
16 p.
|
artikel
|
| 42 |
Synthesis and biological activity of some new flavonyl-2,4-thiazolidinediones
|
Bozdağ-Dündar, Oya
|
|
2008
|
16 |
14 |
p. 6747-6751
5 p.
|
artikel
|
| 43 |
Synthesis and cytotoxic activities of usnic acid derivatives
|
Bazin, Marc-Antoine
|
|
2008
|
16 |
14 |
p. 6860-6866
7 p.
|
artikel
|
| 44 |
Synthesis and evaluation of unsymmetrical polyamine derivatives as antitumor agents
|
Wang, Jianhong
|
|
2008
|
16 |
14 |
p. 7005-7012
8 p.
|
artikel
|
| 45 |
Synthesis and monoamine transporter binding properties of 2β-[3′-(substituted benzyl)isoxazol-5-yl]- and 2β-[3′-methyl-4′-(substituted phenyl)isoxazol-5-yl]-3β-(substituted phenyl)tropanes
|
Jin, Chunyang
|
|
2008
|
16 |
14 |
p. 6682-6688
7 p.
|
artikel
|
| 46 |
Synthesis and pharmacological investigation of novel 2-aminothiazole-privileged aporphines
|
Liu, Zhili
|
|
2008
|
16 |
14 |
p. 6675-6681
7 p.
|
artikel
|
| 47 |
Synthesis and proteasome inhibition of glycyrrhetinic acid derivatives
|
Huang, Li
|
|
2008
|
16 |
14 |
p. 6696-6701
6 p.
|
artikel
|
| 48 |
Synthesis, biological evaluation and molecular modelling of N-heterocyclic dipeptide aldehydes as selective calpain inhibitors
|
Jones, Matthew A.
|
|
2008
|
16 |
14 |
p. 6911-6923
13 p.
|
artikel
|
| 49 |
Synthesis, human telomerase inhibition and anti-proliferative studies of a series of 2,7-bis-substituted amido-anthraquinone derivatives
|
Huang, Hsu-Shan
|
|
2008
|
16 |
14 |
p. 6976-6986
11 p.
|
artikel
|
| 50 |
The use of natural product scaffolds as leads in the search for trypanothione reductase inhibitors
|
Galarreta, Betty C.
|
|
2008
|
16 |
14 |
p. 6689-6695
7 p.
|
artikel
|
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