nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A combined spectroscopic and crystallographic approach to probing drug–human serum albumin interactions
|
Buttar, David |
|
2010 |
18 |
21 |
p. 7486-7496 11 p. |
artikel |
2 |
A convenient synthesis and molecular modeling study of novel purine and pyrimidine derivatives as CDK2/cyclin A3 inhibitors
|
Hamad Elgazwy, Abdel-Sattar S. |
|
2010 |
18 |
21 |
p. 7639-7650 12 p. |
artikel |
3 |
A histone deacetylase-dependent screen in yeast
|
Weerasinghe, Sujith V.W. |
|
2010 |
18 |
21 |
p. 7586-7592 7 p. |
artikel |
4 |
1,6-AnhMurNAc derivatives for assay development of amidase AmiD
|
Mercier, Frédéric |
|
2010 |
18 |
21 |
p. 7422-7431 10 p. |
artikel |
5 |
1,3-Benzoxazole-4-carbonitrile as a novel antifungal scaffold of β-1,6-glucan synthesis inhibitors
|
Kuroyanagi, Jun-ichi |
|
2010 |
18 |
21 |
p. 7593-7606 14 p. |
artikel |
6 |
Binding of diarrheic shellfish poisoning toxins to okadaic acid binding proteins purified from the sponge Halichondria okadai
|
Konoki, Keiichi |
|
2010 |
18 |
21 |
p. 7607-7610 4 p. |
artikel |
7 |
Building a MCHR1 homology model provides insight into the receptor–antagonist contacts that are important for the development of new anti-obesity agents
|
Cirauqui, Nuria |
|
2010 |
18 |
21 |
p. 7365-7379 15 p. |
artikel |
8 |
Corrigendum to “Identification of novel antitubercular compounds through hybrid virtual screening approach” [Bioorg. Med. Chem. 18 (2010) 6914]
|
Muddassar, Muhammad |
|
2010 |
18 |
21 |
p. 7700- 1 p. |
artikel |
9 |
Design of more potent squalene synthase inhibitors with multiple activities
|
Kourounakis, Angeliki P. |
|
2010 |
18 |
21 |
p. 7402-7412 11 p. |
artikel |
10 |
Design, solid-phase synthesis, and biological evaluation of novel 1,5-diarylpyrrole-3-carboxamides as carbonic anhydrase IX inhibitors
|
Gluszok, Sébastien |
|
2010 |
18 |
21 |
p. 7392-7401 10 p. |
artikel |
11 |
Design, synthesis, and biological evaluation of dibromotyrosine analogues inspired by marine natural products as inhibitors of human prostate cancer proliferation, invasion, and migration
|
Sallam, Asmaa A. |
|
2010 |
18 |
21 |
p. 7446-7457 12 p. |
artikel |
12 |
Design, synthesis, and evaluation of an α-tocopherol analogue as a mitochondrial antioxidant
|
Lu, Jun |
|
2010 |
18 |
21 |
p. 7628-7638 11 p. |
artikel |
13 |
Design, synthesis, and subtype selectivity of 3,6-disubstituted β-carbolines at Bz/GABA(A)ergic receptors. SAR and studies directed toward agents for treatment of alcohol abuse
|
Yin, Wenyuan |
|
2010 |
18 |
21 |
p. 7548-7564 17 p. |
artikel |
14 |
9-Dihydroerythromycin ethers as motilin agonists—Developing structure–activity relationships for potency and safety
|
Liu, Yaoquan |
|
2010 |
18 |
21 |
p. 7651-7658 8 p. |
artikel |
15 |
Discovery of {1-[4-(2-{hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl}-1H-benzimidazol-1-yl)piperidin-1-yl]cyclooctyl}methanol, systemically potent novel non-peptide agonist of nociceptin/orphanin FQ receptor as analgesic for the treatment of neuropathic pain: Design, synthesis, and structure–activity relationships
|
Hayashi, Shigeo |
|
2010 |
18 |
21 |
p. 7675-7699 25 p. |
artikel |
16 |
3D QSAR study, synthesis, and in vitro evaluation of (+)-5-FBVM as potential PET radioligand for the vesicular acetylcholine transporter (VAChT)
|
Kovac, Mitja |
|
2010 |
18 |
21 |
p. 7659-7667 9 p. |
artikel |
17 |
Editorial board
|
|
|
2010 |
18 |
21 |
p. IFC- 1 p. |
artikel |
18 |
Fluorescent-tagged sp2-iminosugars with potent β-glucosidase inhibitory activity
|
Aguilar-Moncayo, Matilde |
|
2010 |
18 |
21 |
p. 7439-7445 7 p. |
artikel |
19 |
Graphical contents list
|
|
|
2010 |
18 |
21 |
p. 7321-7330 10 p. |
artikel |
20 |
2-Hexadecynoic acid inhibits plasmodial FAS-II enzymes and arrests erythrocytic and liver stage Plasmodium infections
|
Tasdemir, Deniz |
|
2010 |
18 |
21 |
p. 7475-7485 11 p. |
artikel |
21 |
Indapamide-like benzenesulfonamides as inhibitors of carbonic anhydrases I, II, VII, and XIII
|
Čapkauskaitė, Edita |
|
2010 |
18 |
21 |
p. 7357-7364 8 p. |
artikel |
22 |
In vitro anti-rotavirus activity of polyphenol compounds isolated from the roots of Glycyrrhiza uralensis
|
Kwon, Hyung-Jun |
|
2010 |
18 |
21 |
p. 7668-7674 7 p. |
artikel |
23 |
Novel synthetic 2-amino-10-(3,5-dimethoxy)benzyl-9(10H)-acridinone derivatives as potent DNA-binding antiproliferative agents
|
Gao, Chunmei |
|
2010 |
18 |
21 |
p. 7507-7514 8 p. |
artikel |
24 |
4-[N-(Substituted 4-pyrimidinyl)amino]benzenesulfonamides as inhibitors of carbonic anhydrase isozymes I, II, VII, and XIII
|
Sūdžius, Jurgis |
|
2010 |
18 |
21 |
p. 7413-7421 9 p. |
artikel |
25 |
3-O-Arylmethylgalangin, a novel isostere for anti-HCV 1,3-diketoacids (DKAs)
|
Lee, Hyo Seon |
|
2010 |
18 |
21 |
p. 7331-7337 7 p. |
artikel |
26 |
Polyamide Amino Acids trimers as TAR RNA ligands and anti-HIV agents
|
Bonnard, Vanessa |
|
2010 |
18 |
21 |
p. 7432-7438 7 p. |
artikel |
27 |
Small molecule peptidomimetic inhibitors of importin α/β mediated nuclear transport
|
Ambrus, Géza |
|
2010 |
18 |
21 |
p. 7611-7620 10 p. |
artikel |
28 |
Small molecules targeting the interaction between HIV-1 integrase and LEDGF/p75 cofactor
|
De Luca, Laura |
|
2010 |
18 |
21 |
p. 7515-7521 7 p. |
artikel |
29 |
Synthesis and antitumour activity of glycyrrhetinic acid derivatives
|
Schwarz, Stefan |
|
2010 |
18 |
21 |
p. 7458-7474 17 p. |
artikel |
30 |
Synthesis and biological evaluation of radio-iodinated benzimidazoles as SPECT imaging agents for NR2B subtype of NMDA receptor
|
Fuchigami, Takeshi |
|
2010 |
18 |
21 |
p. 7497-7506 10 p. |
artikel |
31 |
Synthesis and evaluation of benzoxazole derivatives as 5-lipoxygenase inhibitors
|
Song, Hyunmin |
|
2010 |
18 |
21 |
p. 7580-7585 6 p. |
artikel |
32 |
Synthesis and evaluation of macrocyclic amino acid derivatives for tumor imaging by gallium-68 positron emission tomography
|
Shetty, Dinesh |
|
2010 |
18 |
21 |
p. 7338-7347 10 p. |
artikel |
33 |
Synthesis and in vitro antiviral activities of 3′-fluoro (or chloro) and 2′,3′-difluoro 2′,3′-dideoxynucleoside analogs against hepatitis B and C viruses
|
Srivastav, Naveen C. |
|
2010 |
18 |
21 |
p. 7542-7547 6 p. |
artikel |
34 |
Synthesis and structural properties of oligonucleotides covalently linked to acridine and quindoline derivatives through a threoninol linker
|
Aviñó, Anna |
|
2010 |
18 |
21 |
p. 7348-7356 9 p. |
artikel |
35 |
Synthesis, NMR characterization and divergent biological actions of 2′-hydroxy-ceramide/dihydroceramide stereoisomers in MCF7 cells
|
Szulc, Zdzislaw M. |
|
2010 |
18 |
21 |
p. 7565-7579 15 p. |
artikel |
36 |
Synthesis of novel 3-amino and 29-hydroxamic acid derivatives of glycyrrhetinic acid as selective 11β-hydroxysteroid dehydrogenase 2 inhibitors
|
Stanetty, Christian |
|
2010 |
18 |
21 |
p. 7522-7541 20 p. |
artikel |
37 |
The synthesis and biologic evaluation of anti-platelet and cytotoxic β-nitrostyrenes
|
Hsieh, Pei-Wen |
|
2010 |
18 |
21 |
p. 7621-7627 7 p. |
artikel |
38 |
Towards a systematic characterization of the antiprotozoal activity landscape of benzimidazole derivatives
|
Pérez-Villanueva, Jaime |
|
2010 |
18 |
21 |
p. 7380-7391 12 p. |
artikel |