| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A 9-cis-epoxycarotenoid dioxygenase inhibitor for use in the elucidation of abscisic acid action mechanisms
|
Kitahata, Nobutaka
|
|
2006
|
14 |
16 |
p. 5555-5561
7 p.
|
artikel
|
| 2 |
5-Alkylated thiazolidinones as follicle-stimulating hormone (FSH) receptor agonists
|
Wrobel, Jay
|
|
2006
|
14 |
16 |
p. 5729-5741
13 p.
|
artikel
|
| 3 |
An easy preparation of ‘monolithic type’ hydrophilic solid phase: Capability for affinity resin to isolate target proteins
|
Mori, Tomoko
|
|
2006
|
14 |
16 |
p. 5549-5554
6 p.
|
artikel
|
| 4 |
Anticancer activities of some newly synthesized pyridine, pyrane, and pyrimidine derivatives
|
Amr, Abdel-Galil E.
|
|
2006
|
14 |
16 |
p. 5481-5488
8 p.
|
artikel
|
| 5 |
Antikinetoplastid antimitotic activity and metabolic stability of dinitroaniline sulfonamides and benzamides
|
George, Tesmol G.
|
|
2006
|
14 |
16 |
p. 5699-5710
12 p.
|
artikel
|
| 6 |
Application of multicomponent reactions to antimalarial drug discovery. Part 2: New antiplasmodial and antitrypanosomal 4-aminoquinoline γ- and δ-lactams via a ‘catch and release’ protocol
|
Musonda, Chitalu C.
|
|
2006
|
14 |
16 |
p. 5605-5615
11 p.
|
artikel
|
| 7 |
Artepillin C isoprenomics: Design and synthesis of artepillin C isoprene analogues as lipid peroxidation inhibitor having low mitochondrial toxicity
|
Uto, Yoshihiro
|
|
2006
|
14 |
16 |
p. 5721-5728
8 p.
|
artikel
|
| 8 |
Caulerpenyne–colchicine hybrid: Synthesis and biological evaluation
|
Bourdron, Julien
|
|
2006
|
14 |
16 |
p. 5540-5548
9 p.
|
artikel
|
| 9 |
Design, synthesis, SAR, and biological evaluation of new 4-(phenylamino)thieno[2,3-b]pyridine derivatives
|
Rolim Bernardino, Alice Maria
|
|
2006
|
14 |
16 |
p. 5765-5770
6 p.
|
artikel
|
| 10 |
Discovery of new chemical leads for selective EP1 receptor antagonists
|
Naganawa, Atsushi
|
|
2006
|
14 |
16 |
p. 5562-5577
16 p.
|
artikel
|
| 11 |
DNA-binding affinities and sequence selectivity of quaternary benzophenanthridine alkaloids sanguinarine, chelerythrine, and nitidine
|
Bai, Li-Ping
|
|
2006
|
14 |
16 |
p. 5439-5445
7 p.
|
artikel
|
| 12 |
Editorial Board
|
|
|
2006
|
14 |
16 |
p. CO2-
1 p.
|
artikel
|
| 13 |
Exploration of orally available calpain inhibitors. Part 3: Dipeptidyl α-ketoamide derivatives containing pyridine moiety
|
Shirasaki, Yoshihisa
|
|
2006
|
14 |
16 |
p. 5691-5698
8 p.
|
artikel
|
| 14 |
4′-Fluorinated carbocyclic nucleosides: Synthesis and inhibitory activity against S-adenosyl-l-homocysteine hydrolase
|
Kitade, Yukio
|
|
2006
|
14 |
16 |
p. 5578-5583
6 p.
|
artikel
|
| 15 |
Graphical contents list
|
|
|
2006
|
14 |
16 |
p. 5429-5438
10 p.
|
artikel
|
| 16 |
8-Hydroxyquinoline derivatives induce the proliferation of rat mesenchymal stem cells (rMSCs)
|
Zeng, He-Ping
|
|
2006
|
14 |
16 |
p. 5446-5450
5 p.
|
artikel
|
| 17 |
Improving anti-trypanosomal activity of 3-aminoquinoxaline-2-carbonitrile N 1,N 4-dioxide derivatives by complexation with vanadium
|
Urquiola, Carolina
|
|
2006
|
14 |
16 |
p. 5503-5509
7 p.
|
artikel
|
| 18 |
Instructions to contributors
|
|
|
2006
|
14 |
16 |
p. I-
1 p.
|
artikel
|
| 19 |
Ligands with a 3,3-diphenylpentane skeleton for nuclear vitamin D and androgen receptors: Dual activities and metabolic activation
|
Hosoda, Shinnosuke
|
|
2006
|
14 |
16 |
p. 5489-5502
14 p.
|
artikel
|
| 20 |
Molecular modeling of non-covalent binding of homochiral (3S,3′S)-astaxanthin to matrix metalloproteinase-13 (MMP-13)
|
Bikádi, Zsolt
|
|
2006
|
14 |
16 |
p. 5451-5458
8 p.
|
artikel
|
| 21 |
New analogues of butylated hydroxytoluene as anti-inflammatory and antioxidant agents
|
Ziakas, George N.
|
|
2006
|
14 |
16 |
p. 5616-5624
9 p.
|
artikel
|
| 22 |
Novel benzofuran inhibitors of human mitogen-activated protein kinase phosphatase-1
|
Lazo, John S.
|
|
2006
|
14 |
16 |
p. 5643-5650
8 p.
|
artikel
|
| 23 |
Novel 2-substituted nitronyl nitroxides as free radical scavengers: Synthesis, biological evaluation and structure–activity relationship
|
Wu, Yihui
|
|
2006
|
14 |
16 |
p. 5711-5720
10 p.
|
artikel
|
| 24 |
One novel quinoxaline derivative as a potent human cyclophilin A inhibitor shows highly inhibitory activity against mouse spleen cell proliferation
|
Li, Jian
|
|
2006
|
14 |
16 |
p. 5527-5534
8 p.
|
artikel
|
| 25 |
Phosphatidylinositol mannosides: Synthesis and suppression of allergic airway disease
|
Ainge, Gary D.
|
|
2006
|
14 |
16 |
p. 5632-5642
11 p.
|
artikel
|
| 26 |
Regiocontrolled synthesis and HIV inhibitory activity of unsymmetrical binaphthoquinone and trimeric naphthoquinone derivatives of conocurvone
|
Stagliano, Kenneth W.
|
|
2006
|
14 |
16 |
p. 5651-5665
15 p.
|
artikel
|
| 27 |
Structure–activity studies on the protection of Trimetazidine derivatives modified with nitroxides and their precursors from myocardial ischemia–reperfusion injury
|
Kálai, Tamás
|
|
2006
|
14 |
16 |
p. 5510-5516
7 p.
|
artikel
|
| 28 |
Synthesis and antibacterial activity of novel C12 ethyl ketolides
|
Burger, Matthew T.
|
|
2006
|
14 |
16 |
p. 5592-5604
13 p.
|
artikel
|
| 29 |
Synthesis and biological evaluation of purine derivatives incorporating metal chelating ligands as HIV integrase inhibitors
|
Li, Xingnan
|
|
2006
|
14 |
16 |
p. 5742-5755
14 p.
|
artikel
|
| 30 |
Synthesis and evaluation of acridine- and acridone-based anti-herpes agents with topoisomerase activity
|
Goodell, John R.
|
|
2006
|
14 |
16 |
p. 5467-5480
14 p.
|
artikel
|
| 31 |
Synthesis and evaluation of 5,5-diphenylimidazolones as potent human neuropeptide Y5 receptor antagonists
|
Gillman, Kevin W.
|
|
2006
|
14 |
16 |
p. 5517-5526
10 p.
|
artikel
|
| 32 |
Synthesis and evaluation of glycosidase inhibitory activity of N-butyl 1-deoxy-d-gluco-homonojirimycin and N-butyl 1-deoxy-l-ido-homonojirimycin
|
Markad, Shankar D.
|
|
2006
|
14 |
16 |
p. 5535-5539
5 p.
|
artikel
|
| 33 |
Synthesis and high-throughput evaluation of triskelion uracil libraries for inhibition of human dUTPase and UNG2
|
Jiang, Yu Lin
|
|
2006
|
14 |
16 |
p. 5666-5672
7 p.
|
artikel
|
| 34 |
Synthesis and pharmacological activities of xanthone derivatives as α-glucosidase inhibitors
|
Liu, Yan
|
|
2006
|
14 |
16 |
p. 5683-5690
8 p.
|
artikel
|
| 35 |
Synthesis of 7-chloro-5-trifluoromethyl/7-fluoro/7-trifluoromethyl-4H-1,4-benzothiazines as antimicrobial agents
|
Rathore, Bhawani Singh
|
|
2006
|
14 |
16 |
p. 5678-5682
5 p.
|
artikel
|
| 36 |
Synthesis of Sansalvamide A derivatives and their cytotoxicity in the MSS colon cancer cell line HT-29
|
Styers, Thomas J.
|
|
2006
|
14 |
16 |
p. 5625-5631
7 p.
|
artikel
|
| 37 |
The conjugates of uracil–cyclen Zn(II) complexes: Synthesis, characterization, and their interaction with plasmid DNA
|
Xia, Chuan-Qin
|
|
2006
|
14 |
16 |
p. 5756-5764
9 p.
|
artikel
|
| 38 |
The new models of the human telomere d[AGGG(TTAGGG)3] in K+ solution
|
Xu, Yan
|
|
2006
|
14 |
16 |
p. 5584-5591
8 p.
|
artikel
|
| 39 |
Topical anti-inflammatory activity of 2α-hydroxy pentacyclic triterpene acids from the leaves of Ugni molinae
|
Aguirre, María C.
|
|
2006
|
14 |
16 |
p. 5673-5677
5 p.
|
artikel
|
| 40 |
Trypanocidal agents with low cytotoxicity to mammalian cell line: A comparison of the theoretical and biological features of lapachone derivatives
|
Ferreira, Vitor F.
|
|
2006
|
14 |
16 |
p. 5459-5466
8 p.
|
artikel
|
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