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                             50 results found
no title author magazine year volume issue page(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.
 article
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.
 article
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.
 article
4 Antileishmanial activity screening of 5-nitro-2-heterocyclic benzylidene hydrazides Rando, Daniela G.
 2008
 16 14 p. 6724-6731
8 p.
 article
5 Antiprion activity of functionalized 9-aminoacridines related to quinacrine Nguyen Thi, Hanh Thuy
 2008
 16 14 p. 6737-6746
10 p.
 article
6 Anti-retroviral and cytostatic activity of 2′,3′-dideoxyribonucleoside 3′-disulfides Gerland, Béatrice
 2008
 16 14 p. 6824-6831
8 p.
 article
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.
 article
8 BACE1 inhibitory effects of lavandulyl flavanones from Sophora flavescens Hwang, Eun Mi
 2008
 16 14 p. 6669-6674
6 p.
 article
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.
 article
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.
 article
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.
 article
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.
 article
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.
 article
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.
 article
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.
 article
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.
 article
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.
 article
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.
 article
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.
 article
20 Editorial board 2008
 16 14 p. IFC-
1 p.
 article
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.
 article
22 Graphical contents list 2008
 16 14 p. 6651-6662
12 p.
 article
23 Halicyclamine A, a marine spongean alkaloid as a lead for anti-tuberculosis agent Arai, Masayoshi
 2008
 16 14 p. 6732-6736
5 p.
 article
24 Instructions to contributors 2008
 16 14 p. I-
1 p.
 article
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.
 article
26 Ligands to the (IRAP)/AT4 receptor encompassing a 4-hydroxydiphenylmethane scaffold replacing Tyr2 Andersson, Hanna
 2008
 16 14 p. 6924-6935
12 p.
 article
27 Locking the two ends of tetrapeptidic HTLV-I protease inhibitors inside the enzyme Zhang, Meihui
 2008
 16 14 p. 6880-6890
11 p.
 article
28 Mixed tetraoxanes containing the acetone subunit as antimalarials Opsenica, Dejan M.
 2008
 16 14 p. 7039-7045
7 p.
 article
29 N-Arylmethyl substituted iminoribitol derivatives as inhibitors of a purine specific nucleoside hydrolase Goeminne, Annelies
 2008
 16 14 p. 6752-6763
12 p.
 article
30 New trypanocidal hybrid compounds from the association of hydrazone moieties and benzofuroxan heterocycle Porcal, Williams
 2008
 16 14 p. 6995-7004
10 p.
 article
31 2-N-Methyl modifications and SAR studies of manzamine A Ibrahim, Mohamed A.
 2008
 16 14 p. 6702-6706
5 p.
 article
32 Novel aminopeptidase N inhibitors derived from 1,3,4-thiadiazole scaffold Tu, GuoGang
 2008
 16 14 p. 6663-6668
6 p.
 article
33 Novel amodiaquine congeners as potent antimalarial agents Casagrande, Manolo
 2008
 16 14 p. 6813-6823
11 p.
 article
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.
 article
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.
 article
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.
 article
37 Selective angiotensin II AT2 receptor agonists: Benzamide structure–activity relationships Wallinder, Charlotta
 2008
 16 14 p. 6841-6849
9 p.
 article
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.
 article
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.
 article
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.
 article
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.
 article
42 Synthesis and biological activity of some new flavonyl-2,4-thiazolidinediones Bozdağ-Dündar, Oya
 2008
 16 14 p. 6747-6751
5 p.
 article
43 Synthesis and cytotoxic activities of usnic acid derivatives Bazin, Marc-Antoine
 2008
 16 14 p. 6860-6866
7 p.
 article
44 Synthesis and evaluation of unsymmetrical polyamine derivatives as antitumor agents Wang, Jianhong
 2008
 16 14 p. 7005-7012
8 p.
 article
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.
 article
46 Synthesis and pharmacological investigation of novel 2-aminothiazole-privileged aporphines Liu, Zhili
 2008
 16 14 p. 6675-6681
7 p.
 article
47 Synthesis and proteasome inhibition of glycyrrhetinic acid derivatives Huang, Li
 2008
 16 14 p. 6696-6701
6 p.
 article
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.
 article
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.
 article
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.
 article
                             50 results found
 
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