| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A library of novel hydroxamic acids targeting the metallo-protease family: Design, parallel synthesis and screening
|
Flipo, Marion
|
|
2007
|
15 |
1 |
p. 63-76
14 p.
|
artikel
|
| 2 |
Antiprotozoal and antimicrobial activities of O-alkylated and formylated acylphloroglucinols
|
Bharate, Sandip B.
|
|
2007
|
15 |
1 |
p. 87-96
10 p.
|
artikel
|
| 3 |
Antitumor studies. Part 1: Design, synthesis, antitumor activity, and AutoDock study of 2-deoxo-2-phenyl-5-deazaflavins and 2-deoxo-2-phenylflavin-5-oxides as a new class of antitumor agents
|
Ali, Hamed I.
|
|
2007
|
15 |
1 |
p. 242-256
15 p.
|
artikel
|
| 4 |
A Pd(0) based cross-coupling approach to the synthesis of 2-amidopurines and their evaluation as CDK inhibitors
|
Vandromme, Lucie
|
|
2007
|
15 |
1 |
p. 130-141
12 p.
|
artikel
|
| 5 |
Apoptosis induction and modulation of P-glycoprotein mediated multidrug resistance by new macrocyclic lathyrane-type diterpenoids
|
Duarte, Noélia
|
|
2007
|
15 |
1 |
p. 546-554
9 p.
|
artikel
|
| 6 |
A two stage click-based library of protein tyrosine phosphatase inhibitors
|
Xie, Jian
|
|
2007
|
15 |
1 |
p. 458-473
16 p.
|
artikel
|
| 7 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2007
|
15 |
1 |
p. 586-588
3 p.
|
artikel
|
| 8 |
Chemoselective synthesis of erythromycin A ketolides substituted in the C10-methyl group
|
Gunnes, Sølvi
|
|
2007
|
15 |
1 |
p. 119-129
11 p.
|
artikel
|
| 9 |
Cholinesterase inhibitors: SAR and enzyme inhibitory activity of 3-[ω-(benzylmethylamino)alkoxy]xanthen-9-ones
|
Piazzi, Lorna
|
|
2007
|
15 |
1 |
p. 575-585
11 p.
|
artikel
|
| 10 |
Complanadines C and D, new dimeric alkaloids from Lycopodium complanatum
|
Ishiuchi, Kan’ichiro
|
|
2007
|
15 |
1 |
p. 413-417
5 p.
|
artikel
|
| 11 |
Design and synthesis of Rho kinase inhibitors (II)
|
Iwakubo, Masayuki
|
|
2007
|
15 |
1 |
p. 350-364
15 p.
|
artikel
|
| 12 |
Design of bioavailable derivatives of 12-(3-adamantan-1-yl-ureido)dodecanoic acid, a potent inhibitor of the soluble epoxide hydrolase
|
Kim, In-Hae
|
|
2007
|
15 |
1 |
p. 312-323
12 p.
|
artikel
|
| 13 |
Design of endoperoxides with anti-Candida activity
|
Avery, Thomas D.
|
|
2007
|
15 |
1 |
p. 36-42
7 p.
|
artikel
|
| 14 |
Design, synthesis and biological activity of selective and orally available TF/FVIIa complex inhibitors containing non-amidine P1 ligands
|
Miura, Masanori
|
|
2007
|
15 |
1 |
p. 160-173
14 p.
|
artikel
|
| 15 |
Design, synthesis, and biological evaluation of novel iso-d-2′,3′-dideoxy-3′-fluorothianucleoside derivatives
|
Kim, Kyung Ran
|
|
2007
|
15 |
1 |
p. 227-234
8 p.
|
artikel
|
| 16 |
Discovery of 7α-substituted dihydrotestosterones as androgen receptor pure antagonists and their structure–activity relationships
|
Tachibana, Kazutaka
|
|
2007
|
15 |
1 |
p. 174-185
12 p.
|
artikel
|
| 17 |
Editorial board
|
|
|
2007
|
15 |
1 |
p. CO2-
1 p.
|
artikel
|
| 18 |
Fujita-Ban QSAR analysis and CoMFA study of quinoline antagonists of immunostimulatory CpG-oligodeoxynucleotides
|
Paliakov, Ekaterina
|
|
2007
|
15 |
1 |
p. 324-332
9 p.
|
artikel
|
| 19 |
Graphical contents list
|
|
|
2007
|
15 |
1 |
p. 1-16
16 p.
|
artikel
|
| 20 |
Hybrid molecules between distamycin A and active moieties of antitumor agents
|
Baraldi, Pier Giovanni
|
|
2007
|
15 |
1 |
p. 17-35
19 p.
|
artikel
|
| 21 |
Identification of some novel AHAS inhibitors via molecular docking and virtual screening approach
|
Wang, Jian-Guo
|
|
2007
|
15 |
1 |
p. 374-380
7 p.
|
artikel
|
| 22 |
Instructions to contributors
|
|
|
2007
|
15 |
1 |
p. I-
1 p.
|
artikel
|
| 23 |
Isoindolo[2,1-c]benzo[1,2,4]triazines: A new ring system with antiproliferative activity
|
Diana, Patrizia
|
|
2007
|
15 |
1 |
p. 343-349
7 p.
|
artikel
|
| 24 |
1-Methylpyridinium-4-(4-phenylmethanethiosulfonate) iodide, MTS-MPP+, a novel scanning cysteine accessibility method (SCAM) reagent for monoamine transporter studies
|
Gallardo-Godoy, Alejandra
|
|
2007
|
15 |
1 |
p. 305-311
7 p.
|
artikel
|
| 25 |
Modifications of the pyroglutamic acid and histidine residues in thyrotropin-releasing hormone (TRH) yield analogs with selectivity for TRH receptor type 2 over type 1
|
Kaur, Navneet
|
|
2007
|
15 |
1 |
p. 433-443
11 p.
|
artikel
|
| 26 |
Novel C2–C3′ N-peptide linked macrocyclic taxoids. Part 2: Synthesis and biological activities of docetaxel analogues with a peptide side chain at C2 and their macrocyclic derivatives
|
Larroque, Anne-Laure
|
|
2007
|
15 |
1 |
p. 563-574
12 p.
|
artikel
|
| 27 |
Novel selective inhibitors of neutral endopeptidase for the treatment of female sexual arousal disorder
|
Pryde, David C.
|
|
2007
|
15 |
1 |
p. 142-159
18 p.
|
artikel
|
| 28 |
Novel T-type calcium channel blockers: Dioxoquinazoline carboxamide derivatives
|
Jo, Mi Na
|
|
2007
|
15 |
1 |
p. 365-373
9 p.
|
artikel
|
| 29 |
Prediction of binding for a kind of non-peptic HCV NS3 serine protease inhibitors from plants by molecular docking and MM-PBSA method
|
Li, Xudong
|
|
2007
|
15 |
1 |
p. 220-226
7 p.
|
artikel
|
| 30 |
Reactivity of dimethyl fumarate and methylhydrogen fumarate towards glutathione and N-acetyl-l-cysteine—Preparation of S-substituted thiosuccinic acid esters
|
Schmidt, Thomas J.
|
|
2007
|
15 |
1 |
p. 333-342
10 p.
|
artikel
|
| 31 |
Role of glutamate 243 in the active site of 2-deoxy-scyllo-inosose synthase from Bacillus circulans
|
Hirayama, Toshifumi
|
|
2007
|
15 |
1 |
p. 418-423
6 p.
|
artikel
|
| 32 |
Selection and syntheses of tentacle type peptides as ‘artificial’ lectins against various cell-surface carbohydrates
|
Hyun, Soonsil
|
|
2007
|
15 |
1 |
p. 511-517
7 p.
|
artikel
|
| 33 |
Solid-phase synthesis of a combinatorial library of dihydroceramide analogues and its activity in human alveolar epithelial cells
|
Villorbina, Gemma
|
|
2007
|
15 |
1 |
p. 50-62
13 p.
|
artikel
|
| 34 |
Structural advantage of dendritic poly(l-lysine) for gene delivery into cells
|
Yamagata, Masato
|
|
2007
|
15 |
1 |
p. 526-532
7 p.
|
artikel
|
| 35 |
Structural requirement of chalcones for the inhibitory activity of interleukin-5
|
Yang, Hyun-Mo
|
|
2007
|
15 |
1 |
p. 104-111
8 p.
|
artikel
|
| 36 |
Structure determination of inonotsuoxides A and B and in vivo anti-tumor promoting activity of inotodiol from the sclerotia of Inonotus obliquus
|
Nakata, Tomoko
|
|
2007
|
15 |
1 |
p. 257-264
8 p.
|
artikel
|
| 37 |
Synthesis, analytical behaviour and biological evaluation of new 4-substituted pyrrolo[1,2-a]quinoxalines as antileishmanial agents
|
Guillon, Jean
|
|
2007
|
15 |
1 |
p. 194-210
17 p.
|
artikel
|
| 38 |
Synthesis and antifungal activity of (Z)-5-arylidenerhodanines
|
Sortino, Maximiliano
|
|
2007
|
15 |
1 |
p. 484-494
11 p.
|
artikel
|
| 39 |
Synthesis and antitumor activities of a series of novel quinoxalinhydrazides
|
Grande, Fedora
|
|
2007
|
15 |
1 |
p. 288-294
7 p.
|
artikel
|
| 40 |
Synthesis and biological activities of analogs of d-glucosyl-l-tyrosine, a humoral factor that stimulates transcription of the acyl-CoA binding protein in the pheromone gland of the Silkmoth, Bombyx mori
|
Takahashi, Shunya
|
|
2007
|
15 |
1 |
p. 97-103
7 p.
|
artikel
|
| 41 |
Synthesis and biological evaluation of dihydrofuran-fused perhydrophenanthrenes as a new anti-influenza agent having novel structural characteristic
|
Matsuya, Yuji
|
|
2007
|
15 |
1 |
p. 424-432
9 p.
|
artikel
|
| 42 |
Synthesis and biological evaluation of imidazo[1,2-a]pyridine derivatives as novel PI3 kinase p110α inhibitors
|
Hayakawa, Masahiko
|
|
2007
|
15 |
1 |
p. 403-412
10 p.
|
artikel
|
| 43 |
Synthesis and biological evaluation of phenolic Mannich bases of benzaldehyde and (thio)semicarbazone derivatives against the cysteine protease falcipain-2 and a chloroquine resistant strain of Plasmodium falciparum
|
Chipeleme, Alex
|
|
2007
|
15 |
1 |
p. 273-282
10 p.
|
artikel
|
| 44 |
Synthesis and biophysical evaluation of minor-groove binding C-terminus modified pyrrole and imidazole triamide analogs of distamycin
|
Brown, Toni
|
|
2007
|
15 |
1 |
p. 474-483
10 p.
|
artikel
|
| 45 |
Synthesis and characterization of styrylchromone derivatives as β-amyloid imaging agents
|
Ono, Masahiro
|
|
2007
|
15 |
1 |
p. 444-450
7 p.
|
artikel
|
| 46 |
Synthesis and cytotoxic activity of pyrazino[1,2-b]-isoquinolines, 1-(3-isoquinolyl)isoquinolines, and 6,15-iminoisoquino[3,2-b]-3-benzazocines
|
González, Juan Francisco
|
|
2007
|
15 |
1 |
p. 112-118
7 p.
|
artikel
|
| 47 |
Synthesis and evaluation of antitumor activity of novel N-acyllavendamycin analogues and quinoline-5,8-diones
|
Behforouz, Mohammad
|
|
2007
|
15 |
1 |
p. 495-510
16 p.
|
artikel
|
| 48 |
Synthesis and pharmacological evaluation of some 3-phenyl-2-substituted-3H-quinazolin-4-one as analgesic, anti-inflammatory agents
|
Alagarsamy, V.
|
|
2007
|
15 |
1 |
p. 235-241
7 p.
|
artikel
|
| 49 |
Synthesis and SAR study of novel 7-(pyridinium-3-yl)-carbonyl imidazo[5,1-b]thiazol-2-yl carbapenems
|
Maruyama, Takahisa
|
|
2007
|
15 |
1 |
p. 392-402
11 p.
|
artikel
|
| 50 |
Synthesis and trypanocidal activity of ent-kaurane glycosides
|
Batista, Ronan
|
|
2007
|
15 |
1 |
p. 381-391
11 p.
|
artikel
|
| 51 |
Synthesis, characterization and biological activity of complexes of lanthanum(III) with 2-(1′-phenyl- 2′-carboxyl-3′-aza-n-butyl)-1,10-phenanthroline and 2-(1′-p-phenol-2′-carboxyl-3′-aza-n-butyl)-1,10-phenanthroline
|
Zhao, Guanghua
|
|
2007
|
15 |
1 |
p. 533-540
8 p.
|
artikel
|
| 52 |
Synthesis, in vitro evaluation, and SAR studies of a potential antichagasic 1H-pyrazolo[3,4-b]pyridine series
|
Dias, Luiza R.S.
|
|
2007
|
15 |
1 |
p. 211-219
9 p.
|
artikel
|
| 53 |
Synthesis of a non-cationic, water-soluble perylenetetracarboxylic diimide and its interactions with G-quadruplex-forming DNA
|
Samudrala, Ramakrishna
|
|
2007
|
15 |
1 |
p. 186-193
8 p.
|
artikel
|
| 54 |
Synthesis of 6-chloroisoquinoline-5,8-diones and pyrido[3,4-b]phenazine-5,12-diones and evaluation of their cytotoxicity and DNA topoisomerase II inhibitory activity
|
Kim, Jin Sung
|
|
2007
|
15 |
1 |
p. 451-457
7 p.
|
artikel
|
| 55 |
Synthesis of 5-deazaflavin derivatives and their activation of p53 in cells
|
Wilson, Jennifer M.
|
|
2007
|
15 |
1 |
p. 77-86
10 p.
|
artikel
|
| 56 |
Synthesis of diverse analogues of Oenostacin and their antibacterial activities
|
Srivastava, Vandana
|
|
2007
|
15 |
1 |
p. 518-525
8 p.
|
artikel
|
| 57 |
Synthesis of β-ketophosphonate analogs of glutamyl and glutaminyl adenylate, and selective inhibition of the corresponding bacterial aminoacyl-tRNA synthetases
|
Balg, Christian
|
|
2007
|
15 |
1 |
p. 295-304
10 p.
|
artikel
|
| 58 |
Synthetic cryptolepine inhibits DNA binding of NF-κB
|
Olajide, Olumayokun A.
|
|
2007
|
15 |
1 |
p. 43-49
7 p.
|
artikel
|
| 59 |
The design, synthesis, and biological evaluation of novel substituted purines as HIV-1 Tat–TAR inhibitors
|
Yuan, Dekai
|
|
2007
|
15 |
1 |
p. 265-272
8 p.
|
artikel
|
| 60 |
The synthesis and the in vitro cytotoxicity studies of bisnaphthalimidopropyl polyamine derivatives against colon cancer cells and parasite Leishmania infantum
|
Oliveira, João
|
|
2007
|
15 |
1 |
p. 541-545
5 p.
|
artikel
|
| 61 |
The triphosphate of β-d-4′-C-ethynyl-2′,3′-dideoxycytidine is the preferred enantiomer substrate for HIV reverse transcriptase
|
Siddiqui, Maqbool A.
|
|
2007
|
15 |
1 |
p. 283-287
5 p.
|
artikel
|
| 62 |
Tri-, tetra- and heptacyclic perylene analogues as new potential antineoplastic agents based on DNA telomerase inhibition
|
Sissi, Claudia
|
|
2007
|
15 |
1 |
p. 555-562
8 p.
|
artikel
|
Tijdschrift beschrijving