| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Aminopyrazolo[1,5-a]pyrimidines as potential inhibitors of Mycobacterium tuberculosis: Structure activity relationships and ADME characterization
|
Soares de Melo, Candice
|
|
2015
|
23 |
22 |
p. 7240-7250
11 p.
|
artikel
|
| 2 |
Androstane derivatives induce apoptotic death in MDA-MB-231 breast cancer cells
|
Jakimov, Dimitar S.
|
|
2015
|
23 |
22 |
p. 7189-7198
10 p.
|
artikel
|
| 3 |
Antisense peptide nucleic acid–peptide conjugates for functional analyses of genes in Pseudomonas aeruginosa
|
Maekawa, Kazuhiko
|
|
2015
|
23 |
22 |
p. 7234-7239
6 p.
|
artikel
|
| 4 |
1-Benzyl-2-methyl-3-indolylmethylene barbituric acid derivatives: Anti-cancer agents that target nucleophosmin 1 (NPM1)
|
Penthala, Narsimha Reddy
|
|
2015
|
23 |
22 |
p. 7226-7233
8 p.
|
artikel
|
| 5 |
Bivalent ligands incorporating curcumin and diosgenin as multifunctional compounds against Alzheimer’s disease
|
Chojnacki, Jeremy E.
|
|
2015
|
23 |
22 |
p. 7324-7331
8 p.
|
artikel
|
| 6 |
Catecholic amides as potential selective phosphodiesterase 4D inhibitors: Design, synthesis, pharmacological evaluation and structure–activity relationships
|
Zhou, Zhong-Zhen
|
|
2015
|
23 |
22 |
p. 7332-7339
8 p.
|
artikel
|
| 7 |
Design and synthesis of a novel 2-oxindole scaffold as a highly potent and brain-penetrant phosphodiesterase 10A inhibitor
|
Yoshikawa, Masato
|
|
2015
|
23 |
22 |
p. 7138-7149
12 p.
|
artikel
|
| 8 |
Design, synthesis and biological activity of phenoxyacetic acid derivatives as novel free fatty acid receptor 1 agonists
|
Li, Zheng
|
|
2015
|
23 |
22 |
p. 7158-7164
7 p.
|
artikel
|
| 9 |
Editorial board
|
|
|
2015
|
23 |
22 |
p. IFC-
1 p.
|
artikel
|
| 10 |
Fine tuning of agonistic/antagonistic activity for vitamin D receptor by 22-alkyl chain length of ligands: 22S-Hexyl compound unexpectedly restored agonistic activity
|
Anami, Yasuaki
|
|
2015
|
23 |
22 |
p. 7274-7281
8 p.
|
artikel
|
| 11 |
Graphical contents list
|
|
|
2015
|
23 |
22 |
p. 7111-7117
7 p.
|
artikel
|
| 12 |
Inhibition of human topoisomerase I and II and anti-proliferative effects on MCF-7 cells by new titanocene complexes
|
Chimento, Adele
|
|
2015
|
23 |
22 |
p. 7302-7312
11 p.
|
artikel
|
| 13 |
Inhibition of mammalian carbonic anhydrase isoforms I–XIV with a series of phenolic acid esters
|
Maresca, Alfonso
|
|
2015
|
23 |
22 |
p. 7181-7188
8 p.
|
artikel
|
| 14 |
Interactions of a potent cyclic peptide inhibitor with the light chain of botulinum neurotoxin A: Insights from X-ray crystallography
|
Kumaran, Desigan
|
|
2015
|
23 |
22 |
p. 7264-7273
10 p.
|
artikel
|
| 15 |
New natural product carbonic anhydrase inhibitors incorporating phenol moieties
|
Karioti, Anastasia
|
|
2015
|
23 |
22 |
p. 7219-7225
7 p.
|
artikel
|
| 16 |
Novel derivatives of nitro-substituted salicylic acids: Synthesis, antimicrobial activity and cytotoxicity
|
Paraskevopoulos, Georgios
|
|
2015
|
23 |
22 |
p. 7292-7301
10 p.
|
artikel
|
| 17 |
Roles of aromatic side chains and template effects of the hydrophobic cavity of a self-assembled peptide nanoarchitecture for anisotropic growth of gold nanocrystals
|
Tomizaki, Kin-ya
|
|
2015
|
23 |
22 |
p. 7282-7291
10 p.
|
artikel
|
| 18 |
Structure–activity relationships of amide–phosphonate derivatives as inhibitors of the human soluble epoxide hydrolase
|
Kim, In-Hae
|
|
2015
|
23 |
22 |
p. 7199-7210
12 p.
|
artikel
|
| 19 |
Synthesis and activities of new indolopyrrolobenzodiazepine derivatives toward acute myeloid leukemia cells
|
Giraud, Francis
|
|
2015
|
23 |
22 |
p. 7313-7323
11 p.
|
artikel
|
| 20 |
Synthesis and biological evaluation of di-aryl urea derivatives as c-Kit inhibitors
|
Ravez, Séverine
|
|
2015
|
23 |
22 |
p. 7340-7347
8 p.
|
artikel
|
| 21 |
Synthesis and biological evaluation of new C-10 substituted dithranol pleiotropic hybrids
|
Bariamis, Stavros E.
|
|
2015
|
23 |
22 |
p. 7251-7263
13 p.
|
artikel
|
| 22 |
Synthesis and evaluation of C-5 modified 2′-deoxyuridine monophosphates as inhibitors of M. tuberculosis thymidylate synthase
|
Alexandrova, Liudmila A.
|
|
2015
|
23 |
22 |
p. 7131-7137
7 p.
|
artikel
|
| 23 |
Synthesis of potent urease inhibitors based on disulfide scaffold and their molecular docking studies
|
Taha, Muhammad
|
|
2015
|
23 |
22 |
p. 7211-7218
8 p.
|
artikel
|
| 24 |
Targeted Shiga toxin–drug conjugates prepared via Cu-free click chemistry
|
Kostova, Vesela
|
|
2015
|
23 |
22 |
p. 7150-7157
8 p.
|
artikel
|
| 25 |
Triazole linked mono carbonyl curcumin-isatin bifunctional hybrids as novel anti tubulin agents: Design, synthesis, biological evaluation and molecular modeling studies
|
Sharma, Sahil
|
|
2015
|
23 |
22 |
p. 7165-7180
16 p.
|
artikel
|
| 26 |
Ultrasmall dual-modality silica nanoparticle drug conjugates: Design, synthesis, and characterization
|
Yoo, Barney
|
|
2015
|
23 |
22 |
p. 7119-7130
12 p.
|
artikel
|
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