| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abscinazole-F1, a conformationally restricted analogue of the plant growth retardant uniconazole and an inhibitor of ABA 8′-hydroxylase CYP707A with no growth-retardant effect
|
Todoroki, Yasushi
|
|
2009
|
17 |
18 |
p. 6620-6630
11 p.
|
artikel
|
| 2 |
A critical electrostatic interaction mediates inhibitor recognition by human asparagine synthetase
|
Ikeuchi, Hideyuki
|
|
2009
|
17 |
18 |
p. 6641-6650
10 p.
|
artikel
|
| 3 |
A new structural class of S-adenosylhomocysteine hydrolase inhibitors
|
Kim, Byung Gyu
|
|
2009
|
17 |
18 |
p. 6707-6714
8 p.
|
artikel
|
| 4 |
Antagonists of the human A2A receptor. Part 6: Further optimization of pyrimidine-4-carboxamides
|
Gillespie, Roger J.
|
|
2009
|
17 |
18 |
p. 6590-6605
16 p.
|
artikel
|
| 5 |
Antioxidant activity of 5,10-dihydroindeno[1,2-b]indoles containing substituents on dihydroindeno part
|
Talaz, Oktay
|
|
2009
|
17 |
18 |
p. 6583-6589
7 p.
|
artikel
|
| 6 |
ω-Conotoxin GVIA mimetics based on an anthranilamide core: Effect of variation in ammonium side chain lengths and incorporation of fluorine
|
Andersson, Asa
|
|
2009
|
17 |
18 |
p. 6659-6670
12 p.
|
artikel
|
| 7 |
Death receptor 5 promoter-enhancing compounds isolated from Catimbium speciosum and their enhancement effect on TRAIL-induced apoptosis
|
Ohtsuki, Takashi
|
|
2009
|
17 |
18 |
p. 6748-6754
7 p.
|
artikel
|
| 8 |
Design, synthesis, and biological evaluation of hydroquinone derivatives as novel inhibitors of the sarco/endoplasmic reticulum calcium ATPase
|
Paula, Stefan
|
|
2009
|
17 |
18 |
p. 6613-6619
7 p.
|
artikel
|
| 9 |
Design, synthesis and cruzain docking of 3-(4-substituted-aryl)-1,2,4-oxadiazole-N-acylhydrazones as anti-Trypanosoma cruzi agents
|
dos Santos Filho, José Mauricio
|
|
2009
|
17 |
18 |
p. 6682-6691
10 p.
|
artikel
|
| 10 |
Design, synthesis and evaluation of flavonoid derivatives as potent AChE inhibitors
|
Sheng, Rong
|
|
2009
|
17 |
18 |
p. 6692-6698
7 p.
|
artikel
|
| 11 |
Discovery of a series of acrylic acids and their derivatives as chemical leads for selective EP3 receptor antagonists
|
Asada, Masaki
|
|
2009
|
17 |
18 |
p. 6567-6582
16 p.
|
artikel
|
| 12 |
E-Combretastatin and E-resveratrol structural modifications: Antimicrobial and cancer cell growth inhibitory β-E-nitrostyrenes
|
Pettit, Robin K.
|
|
2009
|
17 |
18 |
p. 6606-6612
7 p.
|
artikel
|
| 13 |
Editorial board
|
|
|
2009
|
17 |
18 |
p. IFC-
1 p.
|
artikel
|
| 14 |
Evaluation of delocalized lipophilic cationic dyes as delivery vehicles for photosensitizers to mitochondria
|
Ngen, Ethel J.
|
|
2009
|
17 |
18 |
p. 6631-6640
10 p.
|
artikel
|
| 15 |
Furo[3′,2′:3,4]naphtho[1,2-d]imidazole derivatives as potential inhibitors of inflammatory factors in sepsis
|
Tseng, Chih-Hua
|
|
2009
|
17 |
18 |
p. 6773-6779
7 p.
|
artikel
|
| 16 |
Graphical contents list
|
|
|
2009
|
17 |
18 |
p. 6481-6490
10 p.
|
artikel
|
| 17 |
Identification of new agonists of urotensin-II from a cyclic peptide library
|
Odagami, Takenao
|
|
2009
|
17 |
18 |
p. 6742-6747
6 p.
|
artikel
|
| 18 |
Inhibition of ribonuclease A by nucleoside–dibasic acid conjugates
|
Debnath, Joy
|
|
2009
|
17 |
18 |
p. 6491-6495
5 p.
|
artikel
|
| 19 |
Inhibition of S-ribosylhomocysteinase (LuxS) by substrate analogues modified at the ribosyl C-3 position
|
Wnuk, Stanislaw F.
|
|
2009
|
17 |
18 |
p. 6699-6706
8 p.
|
artikel
|
| 20 |
Instructions to contributors
|
|
|
2009
|
17 |
18 |
p. I-
1 p.
|
artikel
|
| 21 |
Novel 2H-isoquinolin-3-ones as antiplasmodial falcipain-2 inhibitors
|
Micale, Nicola
|
|
2009
|
17 |
18 |
p. 6505-6511
7 p.
|
artikel
|
| 22 |
Solution-phase parallel synthesis of substituted chalcones and their antiparasitary activity against Giardia lamblia
|
Montes-Avila, Julio
|
|
2009
|
17 |
18 |
p. 6780-6785
6 p.
|
artikel
|
| 23 |
Substituted 2-arylbenzothiazoles as kinase inhibitors: Hit-to-lead optimization
|
Tasler, Stefan
|
|
2009
|
17 |
18 |
p. 6728-6737
10 p.
|
artikel
|
| 24 |
Substrate specificity effects of lipoxygenase products and inhibitors on soybean lipoxygenase-1
|
Wecksler, Aaron T.
|
|
2009
|
17 |
18 |
p. 6534-6539
6 p.
|
artikel
|
| 25 |
Synthesis and activity of azaterphenyl diamidines against Trypanosoma brucei rhodesiense and Plasmodium falciparum
|
Hu, Laixing
|
|
2009
|
17 |
18 |
p. 6651-6658
8 p.
|
artikel
|
| 26 |
Synthesis and analgesic profile of conformationally constrained N-acylhydrazone analogues: Discovery of novel N-arylideneamino quinazolin-4(3H)-one compounds derived from natural safrole
|
Maia, Rodolfo C.
|
|
2009
|
17 |
18 |
p. 6517-6525
9 p.
|
artikel
|
| 27 |
Synthesis and antimalarial activity of new chloroquine analogues carrying a multifunctional linear side chain
|
Iwaniuk, Daniel P.
|
|
2009
|
17 |
18 |
p. 6560-6566
7 p.
|
artikel
|
| 28 |
Synthesis and biological evaluation of 4-fluoroproline and 4-fluoropyrrolidine-2-acetic acid derivatives as new GABA uptake inhibitors
|
Zhuang, Weiping
|
|
2009
|
17 |
18 |
p. 6540-6546
7 p.
|
artikel
|
| 29 |
Synthesis and GABAA receptor activity of 2,19-sulfamoyl analogues of allopregnanolone
|
Durán, Fernando J.
|
|
2009
|
17 |
18 |
p. 6526-6533
8 p.
|
artikel
|
| 30 |
Synthesis and glycogen phosphorylase inhibitory activity of N-(β-d-glucopyranosyl)amides possessing 1,4-benzodioxane moiety
|
Czakó, Zoltán
|
|
2009
|
17 |
18 |
p. 6738-6741
4 p.
|
artikel
|
| 31 |
Synthesis and molecular modeling of some novel hexahydroindazole derivatives as potent monoamine oxidase inhibitors
|
Gökhan-Kelekçi, Nesrin
|
|
2009
|
17 |
18 |
p. 6761-6772
12 p.
|
artikel
|
| 32 |
Synthesis and pharmacological evaluation of 6-naltrexamine analogs for alcohol cessation
|
Ghirmai, Senait
|
|
2009
|
17 |
18 |
p. 6671-6681
11 p.
|
artikel
|
| 33 |
Synthesis and pharmacological evaluation of novel 1- and 8-substituted-3-furfuryl xanthines as adenosine receptor antagonists
|
Balo, María Carmen
|
|
2009
|
17 |
18 |
p. 6755-6760
6 p.
|
artikel
|
| 34 |
Synthesis and structure–activity relationships of N-aryl(indol-3-yl)glyoxamides as antitumor agents
|
Marchand, Pascal
|
|
2009
|
17 |
18 |
p. 6715-6727
13 p.
|
artikel
|
| 35 |
Synthesis, structure–affinity relationships, and modeling of AMDA analogs at 5-HT2A and H1 receptors: Structural factors contributing to selectivity
|
Shah, Jitesh R.
|
|
2009
|
17 |
18 |
p. 6496-6504
9 p.
|
artikel
|
| 36 |
Synthesis, structure, and antimycobacterial activity of 6-[1(3H)-isobenzofuranylidenemethyl]purines and analogs
|
Brændvang, Morten
|
|
2009
|
17 |
18 |
p. 6512-6516
5 p.
|
artikel
|
| 37 |
Toward establishing structure–activity relationships for oxygenated coumarins as differentiation inducers of promonocytic leukemic cells
|
Riveiro, María E.
|
|
2009
|
17 |
18 |
p. 6547-6559
13 p.
|
artikel
|
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