nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Amide conjugates of ketoprofen and indole as inhibitors of Gli1-mediated transcription in the Hedgehog pathway
|
Mahindroo, Neeraj |
|
2010 |
18 |
13 |
p. 4801-4811 11 p. |
artikel |
2 |
16-Bromoepiandrosterone, an activator of the mammalian immune system, inhibits glucose 6-phosphate dehydrogenase from Trypanosoma cruzi and is toxic to these parasites grown in culture
|
Cordeiro, Artur T. |
|
2010 |
18 |
13 |
p. 4762-4768 7 p. |
artikel |
3 |
Crystallographic and docking studies of purine nucleoside phosphorylase from Mycobacterium tuberculosis
|
Ducati, Rodrigo G. |
|
2010 |
18 |
13 |
p. 4769-4774 6 p. |
artikel |
4 |
Design and synthesis of novel hydroxyalkylaminomethylchromones for their IL-5 inhibitory activity
|
Thanigaimalai, P. |
|
2010 |
18 |
13 |
p. 4625-4629 5 p. |
artikel |
5 |
Discovery of novel purine derivatives with potent and selective inhibitory activity against c-Src tyrosine kinase
|
Huang, He |
|
2010 |
18 |
13 |
p. 4615-4624 10 p. |
artikel |
6 |
[d4U]-Spacer-[HI-236] double-drug inhibitors of HIV-1 reverse-transcriptase
|
Younis, Yassir |
|
2010 |
18 |
13 |
p. 4661-4673 13 p. |
artikel |
7 |
Editorial board
|
|
|
2010 |
18 |
13 |
p. IFC- 1 p. |
artikel |
8 |
Efficient RNA-targeting by the introduction of aromatic stacking in the duplex major groove via 5-(1-phenyl-1,2,3-triazol-4-yl)-2′-deoxyuridines
|
Andersen, Nicolai Krog |
|
2010 |
18 |
13 |
p. 4702-4710 9 p. |
artikel |
9 |
Globostelletins A–I, cytotoxic isomalabaricane derivatives from the marine sponge Rhabdastrella globostellata
|
Li, Jin |
|
2010 |
18 |
13 |
p. 4639-4647 9 p. |
artikel |
10 |
Graphical contents list
|
|
|
2010 |
18 |
13 |
p. 4593-4600 8 p. |
artikel |
11 |
Inhibition of prolyl oligopeptidase with a synthetic unnatural dipeptide
|
Racys, Daugirdas Tomas |
|
2010 |
18 |
13 |
p. 4775-4782 8 p. |
artikel |
12 |
Long-acting anticholinesterases for myasthenia gravis: synthesis and activities of quaternary phenylcarbamates of neostigmine, pyridostigmine and physostigmine
|
Yu, Qian-sheng |
|
2010 |
18 |
13 |
p. 4687-4693 7 p. |
artikel |
13 |
Optimization of isochromanone based urotensin II receptor agonists
|
Lehmann, Fredrik |
|
2010 |
18 |
13 |
p. 4844-4854 11 p. |
artikel |
14 |
Structure-based virtual screening, synthesis and SAR of novel inhibitors of hepatitis C virus NS5B polymerase
|
Talele, Tanaji T. |
|
2010 |
18 |
13 |
p. 4630-4638 9 p. |
artikel |
15 |
Synthesis and antibacterial studies of binaphthyl-based tripeptoids. Part 2
|
Bremner, John B. |
|
2010 |
18 |
13 |
p. 4793-4800 8 p. |
artikel |
16 |
Synthesis and anti breast cancer activity of biphenyl based chalcones
|
Sharma, Anindra |
|
2010 |
18 |
13 |
p. 4711-4720 10 p. |
artikel |
17 |
Synthesis and anti-hepatitis C virus (HCV) activity of 3′-C-substituted-methyl pyrimidine and purine nucleosides
|
Choi, Won Jun |
|
2010 |
18 |
13 |
p. 4812-4820 9 p. |
artikel |
18 |
Synthesis and anti-HIV activity of 2-naphthyl substituted DAPY analogues as non-nucleoside reverse transcriptase inhibitors
|
Liang, Yong-Hong |
|
2010 |
18 |
13 |
p. 4601-4605 5 p. |
artikel |
19 |
Synthesis and antiplasmodial activity of lycorine derivatives
|
Cedrón, Juan C. |
|
2010 |
18 |
13 |
p. 4694-4701 8 p. |
artikel |
20 |
Synthesis and biological evaluation of pyrazole derivatives containing thiourea skeleton as anticancer agents
|
Lv, Peng-Cheng |
|
2010 |
18 |
13 |
p. 4606-4614 9 p. |
artikel |
21 |
Synthesis and biological evaluation of 5-substituted and 4,5-disubstituted-2-arylamino oxazole TRPV1 antagonists
|
Perner, Richard J. |
|
2010 |
18 |
13 |
p. 4821-4829 9 p. |
artikel |
22 |
Synthesis and characterization of novel phenylindoles as potential probes for imaging of β-amyloid plaques in the brain
|
Watanabe, Hiroyuki |
|
2010 |
18 |
13 |
p. 4740-4746 7 p. |
artikel |
23 |
Synthesis and inhibitory activities of novel C-3 substituted azafagomines: A new type of selective inhibitors of α-l-fucosidases
|
Moreno-Clavijo, Elena |
|
2010 |
18 |
13 |
p. 4648-4660 13 p. |
artikel |
24 |
Synthesis and structure–activity relationship of 6-arylureido-3-pyrrol-2-ylmethylideneindolin-2-one derivatives as potent receptor tyrosine kinase inhibitors
|
Khanwelkar, Rahul R. |
|
2010 |
18 |
13 |
p. 4674-4686 13 p. |
artikel |
25 |
Synthesis and structure–affinity relationships of novel small molecule natural product derivatives capable of discriminating between serotonin 5-HT1A, 5-HT2A, 5-HT2C receptor subtypes
|
Cummings, David F. |
|
2010 |
18 |
13 |
p. 4783-4792 10 p. |
artikel |
26 |
Synthesis, DNA-binding ability and anticancer activity of benzothiazole/benzoxazole–pyrrolo[2,1-c][1,4]benzodiazepine conjugates
|
Kamal, Ahmed |
|
2010 |
18 |
13 |
p. 4747-4761 15 p. |
artikel |
27 |
Synthesis of pyrrolo[3,2-h]quinolinones with good photochemotherapeutic activity and no DNA damage
|
Barraja, Paola |
|
2010 |
18 |
13 |
p. 4830-4843 14 p. |
artikel |
28 |
Synthesis, structural elucidation and in vitro antiparasitic activity against Trypanosoma cruzi and Leishmania chagasi parasites of novel tetrahydro-1-benzazepine derivatives
|
Gómez-Ayala, Sandra |
|
2010 |
18 |
13 |
p. 4721-4739 19 p. |
artikel |