| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Alkenyl substituted bicyclic nucleoside analogues retain nanomolar potency against Varicella Zoster Virus
|
McGuigan, Christopher
|
|
2009
|
17 |
8 |
p. 3025-3027
3 p.
|
artikel
|
| 2 |
A new synthesis and an antiviral assessment of the 4′-fluoro derivative of 4′-deoxy-5′-noraristeromycin
|
Yin, Xue-qiang
|
|
2009
|
17 |
8 |
p. 3126-3129
4 p.
|
artikel
|
| 3 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2009
|
17 |
8 |
p. 3218-3220
3 p.
|
artikel
|
| 4 |
Botulinum neurotoxin serotype A inhibitors: Small-molecule mercaptoacetamide analogs
|
Moe, Scott T.
|
|
2009
|
17 |
8 |
p. 3072-3079
8 p.
|
artikel
|
| 5 |
Carbonic anhydrase inhibitors. Inhibition of human erythrocyte isozymes I and II with a series of antioxidant phenols
|
Şentürk, Murat
|
|
2009
|
17 |
8 |
p. 3207-3211
5 p.
|
artikel
|
| 6 |
Carbonic anhydrase inhibitors. The nematode α-carbonic anhydrase of Caenorhabditis elegans CAH-4b is highly inhibited by 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides
|
Güzel, Özlen
|
|
2009
|
17 |
8 |
p. 3212-3215
4 p.
|
artikel
|
| 7 |
Comparing anti-HIV, antibacterial, antifungal, micellar, and cytotoxic properties of tricarboxylato dendritic amphiphiles
|
Macri, Richard V.
|
|
2009
|
17 |
8 |
p. 3162-3168
7 p.
|
artikel
|
| 8 |
Design and synthesis of N-2,6-difluorophenyl-5-methoxyl-1,2,4-triazolo[1,5-a]-pyrimidine-2-sulfonamide as acetohydroxyacid synthase inhibitor
|
Chen, Chao-Nan
|
|
2009
|
17 |
8 |
p. 3011-3017
7 p.
|
artikel
|
| 9 |
Design and synthesis of 3-phenyltetrahydronaphthalenic derivatives as new selective MT2 melatoninergic ligands. Part II
|
Durieux, Sophie
|
|
2009
|
17 |
8 |
p. 2963-2974
12 p.
|
artikel
|
| 10 |
Design, synthesis, antimicrobial activity and molecular modeling studies of novel benzofuroxan derivatives against Staphylococcus aureus
|
Jorge, Salomão Dória
|
|
2009
|
17 |
8 |
p. 3028-3036
9 p.
|
artikel
|
| 11 |
Diether derivatives of homo- or substituted piperidines as non-imidazole histamine H3 receptor ligands
|
Łażewska, Dorota
|
|
2009
|
17 |
8 |
p. 3037-3042
6 p.
|
artikel
|
| 12 |
Discovery of dual inhibitors targeting both HIV-1 capsid and human cyclophilin A to inhibit the assembly and uncoating of the viral capsid
|
Li, Jiebo
|
|
2009
|
17 |
8 |
p. 3177-3188
12 p.
|
artikel
|
| 13 |
Editorial board
|
|
|
2009
|
17 |
8 |
p. IFC-
1 p.
|
artikel
|
| 14 |
Erratum to “Discovery, design, and synthesis of anti-metastatic lead phenylmethylene hydantoins inspired by marine natural products” [Bioorg. Med. Chem. 17 (2009) 1731–1738]
|
Mudit, Mudit
|
|
2009
|
17 |
8 |
p. 3216-3217
2 p.
|
artikel
|
| 15 |
Graphical contents list
|
|
|
2009
|
17 |
8 |
p. 2941-2949
9 p.
|
artikel
|
| 16 |
Identification of novel inhibitors of HCV RNA-dependent RNA polymerase by pharmacophore-based virtual screening and in vitro evaluation
|
Ryu, Kisun
|
|
2009
|
17 |
8 |
p. 2975-2982
8 p.
|
artikel
|
| 17 |
Inhibition of monoamine oxidase B by N-methyl-2-phenylmaleimides
|
Manley-King, Clarina I.
|
|
2009
|
17 |
8 |
p. 3104-3110
7 p.
|
artikel
|
| 18 |
Inhibitory effects of sesquiterpene lactones isolated from Eupatorium chinense L. on IgE-mediated degranulation in rat basophilic leukemia RBL-2H3 cells and passive cutaneous anaphylaxis reaction in mice
|
Itoh, Tomohiro
|
|
2009
|
17 |
8 |
p. 3189-3197
9 p.
|
artikel
|
| 19 |
Instructions to contributors
|
|
|
2009
|
17 |
8 |
p. I-
1 p.
|
artikel
|
| 20 |
Ligustrazine derivatives. Part 3: Design, synthesis and evaluation of novel acylpiperazinyl derivatives as potential cerebrocardiac vascular agents
|
Cheng, Xian-Chao
|
|
2009
|
17 |
8 |
p. 3018-3024
7 p.
|
artikel
|
| 21 |
Nanoparticles in cellular drug delivery
|
Faraji, Amir H.
|
|
2009
|
17 |
8 |
p. 2950-2962
13 p.
|
artikel
|
| 22 |
Novel aminopeptidase N inhibitors derived from antineoplaston AS2–5 (Part I)
|
Li, Xun
|
|
2009
|
17 |
8 |
p. 3053-3060
8 p.
|
artikel
|
| 23 |
Novel aminopeptidase N inhibitors derived from antineoplaston AS2–5 (Part II)
|
Li, Xun
|
|
2009
|
17 |
8 |
p. 3061-3071
11 p.
|
artikel
|
| 24 |
Schiff bases of 3-formylchromone as thymidine phosphorylase inhibitors
|
Khan, Khalid Mohammed
|
|
2009
|
17 |
8 |
p. 2983-2988
6 p.
|
artikel
|
| 25 |
Structural–activity relationship study of highly-functionalized imidazolines as potent inhibitors of nuclear transcription factor-κB mediated IL-6 production
|
Kahlon, Daljinder K.
|
|
2009
|
17 |
8 |
p. 3093-3103
11 p.
|
artikel
|
| 26 |
Structure-based virtual screening of Src kinase inhibitors
|
Lee, Kyungik
|
|
2009
|
17 |
8 |
p. 3152-3161
10 p.
|
artikel
|
| 27 |
Synthesis and anti-hepatitis B virus activities of Matijing-Su derivatives
|
Xu, Bixue
|
|
2009
|
17 |
8 |
p. 3118-3125
8 p.
|
artikel
|
| 28 |
Synthesis and biological evaluation of novel conjugates of podophyllotoxin and 5-FU as antineoplastic agents
|
Chen, Shi-Wu
|
|
2009
|
17 |
8 |
p. 3111-3117
7 p.
|
artikel
|
| 29 |
Synthesis and in vitro affinities of various MDL 100907 derivatives as potential 18F-radioligands for 5-HT2A receptor imaging with PET
|
Herth, Matthias M.
|
|
2009
|
17 |
8 |
p. 2989-3002
14 p.
|
artikel
|
| 30 |
Synthesis and pharmacological evaluation of (2-oxaadamant-1-yl)amines
|
Duque, María D.
|
|
2009
|
17 |
8 |
p. 3198-3206
9 p.
|
artikel
|
| 31 |
Synthesis and structure–activity relationship of novel diarylpyrazole imide analogues as CB1 cannabinoid receptor ligands
|
Song, Kwang-Seop
|
|
2009
|
17 |
8 |
p. 3080-3092
13 p.
|
artikel
|
| 32 |
Synthesis and structure–activity relationships of amide derivatives of (4,4-difluoro-1,2,3,4-tetrahydro-5H-1-benzazepin-5-ylidene)acetic acid as selective arginine vasopressin V2 receptor agonists
|
Tsukamoto, Issei
|
|
2009
|
17 |
8 |
p. 3130-3141
12 p.
|
artikel
|
| 33 |
Synthesis, characterization, toxicity, cytogenetic and in vivo antitumor studies of 1,1-dithiolate Cu(II) complexes with di-, tri-, tetra- amines and 1,3-thiazoles. Structure–activity correlation
|
Bolos, C.A.
|
|
2009
|
17 |
8 |
p. 3142-3151
10 p.
|
artikel
|
| 34 |
Synthesis, cytotoxic and combined cDDP activity of new stable curcumin derivatives
|
Ferrari, Erika
|
|
2009
|
17 |
8 |
p. 3043-3052
10 p.
|
artikel
|
| 35 |
Synthesis of dammarane-type triterpene derivatives and their ability to inhibit HIV and HCV proteases
|
Wei, Ying
|
|
2009
|
17 |
8 |
p. 3003-3010
8 p.
|
artikel
|
| 36 |
The identification of novel PLC-γ inhibitors using virtual high throughput screening
|
Reynisson, Jóhannes
|
|
2009
|
17 |
8 |
p. 3169-3176
8 p.
|
artikel
|
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