| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A-ring hydroxymethyl 19-nor analogs of the natural hormone 1α,25-dihydroxyvitamin D3: synthesis and preliminary biological evaluation
|
Hatcher, Mark A.
|
|
2005
|
13 |
12 |
p. 3964-3976
13 p.
|
artikel
|
| 2 |
Comparison of the anti-influenza virus activity of cyclopentane derivatives with oseltamivir and zanamivir in vivo
|
Chand, Pooran
|
|
2005
|
13 |
12 |
p. 4071-4077
7 p.
|
artikel
|
| 3 |
Contributors to this issue
|
|
|
2005
|
13 |
12 |
p. I-
1 p.
|
artikel
|
| 4 |
Corrigendum to “Studies on the cytochrome P450 catalyzed oxidation of 13C labeled 1-cyclopropyl-4-phenyl-1,2,3,6-tetrahydropyridine by 13C NMR”
|
Bissel, Philippe
|
|
2005
|
13 |
12 |
p. 4130-
1 p.
|
artikel
|
| 5 |
Design and synthesis of alkyl 7,7-dihalo-3-methyl-5-(nitrophenyl)-2-azabicyclo[4.1.0]hept-3-ene-4-carboxylates with calcium channel antagonist activity
|
Mojarrad, Javid S.
|
|
2005
|
13 |
12 |
p. 4085-4091
7 p.
|
artikel
|
| 6 |
Design and synthesis of a novel enediynyl pentapeptide with predominantly β-turn structural motif and its potential as a fluorescence-based chemosensor
|
Basak, Amit
|
|
2005
|
13 |
12 |
p. 4096-4102
7 p.
|
artikel
|
| 7 |
Design, synthesis, and biological activity of non-basic compounds as factor Xa inhibitors: SAR study of S1 and aryl binding sites
|
Komoriya, Satoshi
|
|
2005
|
13 |
12 |
p. 3927-3954
28 p.
|
artikel
|
| 8 |
Discovery of an N-(2-aminopyridin-4-ylmethyl)nicotinamide derivative: a potent and orally bioavailable NCX inhibitor
|
Kuramochi, Takahiro
|
|
2005
|
13 |
12 |
p. 4022-4036
15 p.
|
artikel
|
| 9 |
Editorial board
|
|
|
2005
|
13 |
12 |
p. CO2-
1 p.
|
artikel
|
| 10 |
From SAR to comparative QSAR: role of hydrophobicity in the design of 4-hydroxy-5,6-dihydropyran-2-ones HIV-1 protease inhibitors
|
Bhhatarai, Barun
|
|
2005
|
13 |
12 |
p. 4078-4084
7 p.
|
artikel
|
| 11 |
Graphical contents list
|
|
|
2005
|
13 |
12 |
p. 3865-3872
8 p.
|
artikel
|
| 12 |
Identification of bis-quindolines as new antiinfective agents
|
Mardenborough, Leroy G.
|
|
2005
|
13 |
12 |
p. 3955-3963
9 p.
|
artikel
|
| 13 |
Identification of carbon-centred radicals derived from linalyl hydroperoxide, a strong skin sensitizer: a possible route for protein modifications
|
Bezard, Michael
|
|
2005
|
13 |
12 |
p. 3977-3986
10 p.
|
artikel
|
| 14 |
Inclusion complexes of azadirachtin with native and methylated cyclodextrins: solubilization and binding ability
|
Liu, Yu
|
|
2005
|
13 |
12 |
p. 4037-4042
6 p.
|
artikel
|
| 15 |
Indole alkaloids from Tabernaemontana australis (Müell. Arg) Miers that inhibit acetylcholinesterase enzyme
|
Andrade, Marcelo T.
|
|
2005
|
13 |
12 |
p. 4092-4095
4 p.
|
artikel
|
| 16 |
Instructions to contributors
|
|
|
2005
|
13 |
12 |
p. III-VII
nvt p.
|
artikel
|
| 17 |
Interaction of wogonin with bovine serum albumin
|
Tian, Jianniao
|
|
2005
|
13 |
12 |
p. 4124-4129
6 p.
|
artikel
|
| 18 |
Lobelane analogues as novel ligands for the vesicular monoamine transporter-2
|
Zheng, Guangrong
|
|
2005
|
13 |
12 |
p. 3899-3909
11 p.
|
artikel
|
| 19 |
Napthalimidobenzamide DB-51630: a novel DNA binding agent inducing p300 gene expression and exerting a potent anti-cancer activity
|
Suzuki, Kenji
|
|
2005
|
13 |
12 |
p. 4014-4021
8 p.
|
artikel
|
| 20 |
Nitroarylmethylcarbamate prodrugs of doxorubicin for use with nitroreductase gene-directed enzyme prodrug therapy
|
Hay, Michael P.
|
|
2005
|
13 |
12 |
p. 4043-4055
13 p.
|
artikel
|
| 21 |
O 6-3-[125I]iodobenzyl-2′-deoxyguanosine ([125I]IBdG): synthesis and evaluation of its usefulness as an agent for quantification of alkylguanine-DNA alkyltransferase (AGT)
|
Shankar, Sriram
|
|
2005
|
13 |
12 |
p. 3889-3898
10 p.
|
artikel
|
| 22 |
Potent antitumor 9-anilinoacridines bearing an alkylating N-mustard residue on the anilino ring: synthesis and biological activity
|
Bacherikov, Valeriy A.
|
|
2005
|
13 |
12 |
p. 3993-4006
14 p.
|
artikel
|
| 23 |
Synthesis and antibacterial activity of new N-linked 5-triazolylmethyl oxazolidinones
|
Phillips, Oludotun A.
|
|
2005
|
13 |
12 |
p. 4113-4123
11 p.
|
artikel
|
| 24 |
Synthesis and antimycobacterial evaluation of certain fluoroquinolone derivatives
|
Zhao, Yue-Ling
|
|
2005
|
13 |
12 |
p. 3921-3926
6 p.
|
artikel
|
| 25 |
Synthesis and biological evaluation of aromatic enones related to curcumin
|
Robinson, Thomas Philip
|
|
2005
|
13 |
12 |
p. 4007-4013
7 p.
|
artikel
|
| 26 |
Synthesis and characterization of azole isoflavone inhibitors of aromatase
|
Hackett, John C
|
|
2005
|
13 |
12 |
p. 4063-4070
8 p.
|
artikel
|
| 27 |
Synthesis and structure–activity relationship of ethacrynic acid analogues on glutathione-s-transferase P1-1 activity inhibition
|
Zhao, Guisen
|
|
2005
|
13 |
12 |
p. 4056-4062
7 p.
|
artikel
|
| 28 |
Synthesis, immunological activities, and scavenging ability toward superoxide anion of (1→3)-β-d-pentaglucoside and its epoxyalkyl derivatives
|
Huang, Gang-Liang
|
|
2005
|
13 |
12 |
p. 3873-3877
5 p.
|
artikel
|
| 29 |
Synthesis of arylidene-substituted gelastatin analogues and their screening for MMP-2 inhibitory activity
|
Kim, Eun Jin
|
|
2005
|
13 |
12 |
p. 4103-4112
10 p.
|
artikel
|
| 30 |
Synthesis of glycoporphyrin derivatives and their antiviral activity against herpes simplex virus types 1 and 2
|
Tomé, João P.C.
|
|
2005
|
13 |
12 |
p. 3878-3888
11 p.
|
artikel
|
| 31 |
Synthetic modification of the 2-oxypropionic acid moiety in 2-{4-[(7-chloro-2-quinoxalinyl)oxy]phenoxy}propionic acid (XK469), and consequent antitumor effects. Part 4
|
Hazeldine, Stuart T.
|
|
2005
|
13 |
12 |
p. 3910-3920
11 p.
|
artikel
|
| 32 |
Theoretical study revealing the functioning of a novel combination of catalytic motifs in histone deacetylase
|
Vanommeslaeghe, K.
|
|
2005
|
13 |
12 |
p. 3987-3992
6 p.
|
artikel
|
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