| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Aplysinopsin analogs: Synthesis and anti-proliferative activity of substituted (Z)-5-(N-benzylindol-3-ylmethylene)imidazolidine-2,4-diones
|
Thirupathi Reddy, Y.
|
|
2010
|
18 |
10 |
p. 3570-3574
5 p.
|
artikel
|
| 2 |
Bioactive norditerpenoids from the soft coral Sinularia gyrosa
|
Cheng, Shi-Yie
|
|
2010
|
18 |
10 |
p. 3379-3386
8 p.
|
artikel
|
| 3 |
Corrigendum to “Chemo-enzymatic synthesis of 1,4-oxazepanyl sugar as potent inhibitor of chitinase” [Bioorg. Med. Chem. 14 (2006) 2446]
|
Huang, Gang-Liang
|
|
2010
|
18 |
10 |
p. 3625-
1 p.
|
artikel
|
| 4 |
1-(3-Deoxy-3-fluoro-β-d-glucopyranosyl) pyrimidine derivatives as inhibitors of glycogen phosphorylase b: Kinetic, crystallographic and modelling studies
|
Tsirkone, Vicky G.
|
|
2010
|
18 |
10 |
p. 3413-3425
13 p.
|
artikel
|
| 5 |
Design of new potent and selective secretory phospholipase A2 inhibitors. 6-Synthesis, structure–activity relationships and molecular modelling of 1-substituted-4-[4,5-dihydro-1,2,4-(4H)-oxadiazol-5-one-3-yl(methyl)]-functionalized aryl piperazin/one/dione derivatives
|
Meddad-Belhabich, Nadia
|
|
2010
|
18 |
10 |
p. 3588-3600
13 p.
|
artikel
|
| 6 |
Design, synthesis and anticancer activities of stilbene-coumarin hybrid compounds: Identification of novel proapoptotic agents
|
Belluti, Federica
|
|
2010
|
18 |
10 |
p. 3543-3550
8 p.
|
artikel
|
| 7 |
Design, synthesis and pharmacological evaluation of novel naphthalenic derivatives as selective MT1 melatoninergic ligands
|
Mésangeau, Christophe
|
|
2010
|
18 |
10 |
p. 3426-3436
11 p.
|
artikel
|
| 8 |
Discovery of GS-9131: Design, synthesis and optimization of amidate prodrugs of the novel nucleoside phosphonate HIV reverse transcriptase (RT) inhibitor GS-9148
|
Mackman, Richard L.
|
|
2010
|
18 |
10 |
p. 3606-3617
12 p.
|
artikel
|
| 9 |
Editorial board
|
|
|
2010
|
18 |
10 |
p. IFC-
1 p.
|
artikel
|
| 10 |
Functionalized pyrazoles and pyrazolo[3,4-d]pyridazinones: Synthesis and evaluation of their phosphodiesterase 4 inhibitory activity
|
Biagini, Pierfrancesco
|
|
2010
|
18 |
10 |
p. 3506-3517
12 p.
|
artikel
|
| 11 |
Graphical contents list
|
|
|
2010
|
18 |
10 |
p. 3353-3360
8 p.
|
artikel
|
| 12 |
In vitro cytotoxic activity of isolated acridones alkaloids from Zanthoxylum leprieurii Guill. et Perr
|
Ngoumfo, Rostand M.
|
|
2010
|
18 |
10 |
p. 3601-3605
5 p.
|
artikel
|
| 13 |
Isolation and characterization of enantioselective DNA aptamers for ibuprofen
|
Kim, Yeon Seok
|
|
2010
|
18 |
10 |
p. 3467-3473
7 p.
|
artikel
|
| 14 |
Mechanism of influence of phosphorylation on serine 124 on a decrease of catalytic activity of human thymidylate synthase
|
Jarmuła, Adam
|
|
2010
|
18 |
10 |
p. 3361-3370
10 p.
|
artikel
|
| 15 |
NO-releasing esters show carbonic anhydrase inhibitory action against human isoforms I and II
|
Ekinci, Deniz
|
|
2010
|
18 |
10 |
p. 3559-3563
5 p.
|
artikel
|
| 16 |
Novel estrone mimetics with high 17β-HSD1 inhibitory activity
|
Oster, Alexander
|
|
2010
|
18 |
10 |
p. 3494-3505
12 p.
|
artikel
|
| 17 |
Photolabile ubiquinone analogues for identification and characterization of quinone binding sites in proteins
|
Pei, Zhichao
|
|
2010
|
18 |
10 |
p. 3457-3466
10 p.
|
artikel
|
| 18 |
RNA interference with 2′,4′-bridged nucleic acid analogues
|
Abdur Rahman, S.M.
|
|
2010
|
18 |
10 |
p. 3474-3480
7 p.
|
artikel
|
| 19 |
Serotonin derivatives as a new class of non-ATP-competitive receptor tyrosine kinase inhibitors
|
Büttner, Anita
|
|
2010
|
18 |
10 |
p. 3387-3402
16 p.
|
artikel
|
| 20 |
Silica-supported fluoroboric acid (HBF4–SiO2) catalyzed highly productive synthesis of thiomorpholides as activators of l-asparaginase as well as the antioxidant agent
|
Bandgar, Babasaheb P.
|
|
2010
|
18 |
10 |
p. 3618-3624
7 p.
|
artikel
|
| 21 |
Structure–activity relationships of carbocyclic 6-benzylthioinosine analogues as subversive substrates of Toxoplasma gondii adenosine kinase
|
Kim, Young Ah
|
|
2010
|
18 |
10 |
p. 3403-3412
10 p.
|
artikel
|
| 22 |
Synthesis and antiprotozoal activity of 2,5-bis[amidinoaryl]thiazoles
|
Branowska, Danuta
|
|
2010
|
18 |
10 |
p. 3551-3558
8 p.
|
artikel
|
| 23 |
Synthesis and biological activity of N 4-phenylsubstituted-6-(2,4-dichloro phenylmethyl)-7H-pyrrolo[2,3-d]pyrimidine-2,4-diamines as vascular endothelial growth factor receptor-2 inhibitors and antiangiogenic and antitumor agents
|
Gangjee, Aleem
|
|
2010
|
18 |
10 |
p. 3575-3587
13 p.
|
artikel
|
| 24 |
Synthesis and biological evaluation of phenolic 4,5-dihydroisoxazoles and 3-hydroxy ketones as estrogen receptor α and β agonists
|
Poutiainen, Pekka K.
|
|
2010
|
18 |
10 |
p. 3437-3447
11 p.
|
artikel
|
| 25 |
Synthesis and evaluation of nitric oxide-releasing derivatives of farnesylthiosalicylic acid as anti-tumor agents
|
Ling, Yong
|
|
2010
|
18 |
10 |
p. 3448-3456
9 p.
|
artikel
|
| 26 |
Synthesis and evaluation of verticipyrone analogues as mitochondrial complex I inhibitors
|
Leiris, Simon J.
|
|
2010
|
18 |
10 |
p. 3481-3493
13 p.
|
artikel
|
| 27 |
Synthesis and opioid activity of novel 6-substituted-6-demethoxy-ethenomorphinans
|
Czakó, Barbara
|
|
2010
|
18 |
10 |
p. 3535-3542
8 p.
|
artikel
|
| 28 |
Synthesis, anticoagulant and PIVKA-II induced by new 4-hydroxycoumarin derivatives
|
Abdelhafez, Omaima M.
|
|
2010
|
18 |
10 |
p. 3371-3378
8 p.
|
artikel
|
| 29 |
Targeting a ruthenium complex to the nucleus with short peptides
|
Puckett, Cindy A.
|
|
2010
|
18 |
10 |
p. 3564-3569
6 p.
|
artikel
|
| 30 |
Virtual screening, selection and development of a benzindolone structural scaffold for inhibition of lumazine synthase
|
Talukdar, Arindam
|
|
2010
|
18 |
10 |
p. 3518-3534
17 p.
|
artikel
|
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