| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel and facile synthesis of tetra branched derivatives of nociceptin/orphanin FQ
|
Guerrini, Remo
|
|
2014
|
22 |
14 |
p. 3703-3712
10 p.
|
artikel
|
| 2 |
Antiplasmodial activity of new 4-aminoquinoline derivatives against chloroquine resistant strain
|
Sinha, Manish
|
|
2014
|
22 |
14 |
p. 3573-3586
14 p.
|
artikel
|
| 3 |
Carbonic anhydrase inhibitors: Synthesis, molecular docking, cytotoxic and inhibition of the human carbonic anhydrase isoforms I, II, IX, XII with novel benzenesulfonamides incorporating pyrrole, pyrrolopyrimidine and fused pyrrolopyrimidine moieties
|
Ghorab, Mostafa M.
|
|
2014
|
22 |
14 |
p. 3684-3695
12 p.
|
artikel
|
| 4 |
Catechol–rhodanine derivatives: Specific and promiscuous inhibitors of Escherichia coli deoxyxylulose phosphate reductoisomerase (DXR)
|
Zinglé, Catherine
|
|
2014
|
22 |
14 |
p. 3713-3719
7 p.
|
artikel
|
| 5 |
Combination of 2-methoxy-3-phenylsulfonylaminobenzamide and 2-aminobenzothiazole to discover novel anticancer agents
|
Li, Huan
|
|
2014
|
22 |
14 |
p. 3739-3748
10 p.
|
artikel
|
| 6 |
Design and synthesis of novel and highly-active pan-histone deacetylase (pan-HDAC) inhibitors
|
Tashima, Toshihiko
|
|
2014
|
22 |
14 |
p. 3720-3731
12 p.
|
artikel
|
| 7 |
Design, synthesis and biological evaluation of novel 6,7-disubstituted-4-phenoxyquinoline derivatives bearing 4-oxo-3,4-dihydrophthalazine-1-carboxamide moieties as c-Met kinase inhibitors
|
Liu, Zijian
|
|
2014
|
22 |
14 |
p. 3642-3653
12 p.
|
artikel
|
| 8 |
Design, synthesis, antiviral and cytostatic activity of ω-(1H-1,2,3-triazol-1-yl)(polyhydroxy)alkylphosphonates as acyclic nucleotide analogues
|
Głowacka, Iwona E.
|
|
2014
|
22 |
14 |
p. 3629-3641
13 p.
|
artikel
|
| 9 |
Editorial board
|
|
|
2014
|
22 |
14 |
p. IFC-
1 p.
|
artikel
|
| 10 |
Graphical contents list
|
|
|
2014
|
22 |
14 |
p. 3545-3550
6 p.
|
artikel
|
| 11 |
Interaction analysis of a ladder-shaped polycyclic ether and model transmembrane peptides in lipid bilayers by using Förster resonance energy transfer and polarized attenuated total reflection infrared spectroscopy
|
Yamada, Kazuya
|
|
2014
|
22 |
14 |
p. 3773-3780
8 p.
|
artikel
|
| 12 |
Macrocyclic diterpenes resensitizing multidrug resistant phenotypes
|
Reis, Mariana A.
|
|
2014
|
22 |
14 |
p. 3696-3702
7 p.
|
artikel
|
| 13 |
New coumarin derivatives: Design, synthesis and use as inhibitors of hMAO
|
He, Xu
|
|
2014
|
22 |
14 |
p. 3732-3738
7 p.
|
artikel
|
| 14 |
Novel 3-arylfuran-2(5H)-one-fluoroquinolone hybrid: Design, synthesis and evaluation as antibacterial agent
|
Wang, Xu-Dong
|
|
2014
|
22 |
14 |
p. 3620-3628
9 p.
|
artikel
|
| 15 |
Novel synthetic route for antimalarial benzo[a]phenoxazine derivative SSJ-183 and two active metabolites
|
Mizukawa, Yuki
|
|
2014
|
22 |
14 |
p. 3749-3752
4 p.
|
artikel
|
| 16 |
4-Quinolone-3-carboxylic acids as cell-permeable inhibitors of protein tyrosine phosphatase 1B
|
Zhi, Ying
|
|
2014
|
22 |
14 |
p. 3670-3683
14 p.
|
artikel
|
| 17 |
Structure–activity relationship study of non-steroidal NPC1L1 ligands identified through cell-based assay using pharmacological chaperone effect as a readout
|
Karaki, Fumika
|
|
2014
|
22 |
14 |
p. 3587-3609
23 p.
|
artikel
|
| 18 |
Sulfur, selenium and tellurium pseudopeptides: Synthesis and biological evaluation
|
Shaaban, Saad
|
|
2014
|
22 |
14 |
p. 3610-3619
10 p.
|
artikel
|
| 19 |
Synthesis and biological evaluation of substituted 3-anilino-quinolin-2(1H)-ones as PDK1 inhibitors
|
O’Brien, Nathan J.
|
|
2014
|
22 |
14 |
p. 3781-3790
10 p.
|
artikel
|
| 20 |
Synthesis and evaluation of (E)-2-(acrylamido)cyclohex-1-enecarboxylic acid derivatives as HCA1, HCA2, and HCA3 receptor agonists
|
Bobileva, Olga
|
|
2014
|
22 |
14 |
p. 3654-3669
16 p.
|
artikel
|
| 21 |
Synthesis of truncated analogues of preptin-(1–16), and investigation of their ability to stimulate osteoblast proliferation
|
Kowalczyk, Renata
|
|
2014
|
22 |
14 |
p. 3565-3572
8 p.
|
artikel
|
| 22 |
The design and discovery of water soluble 4-substituted-2,6-dimethylfuro[2,3-d]pyrimidines as multitargeted receptor tyrosine kinase inhibitors and microtubule targeting antitumor agents
|
Zhang, Xin
|
|
2014
|
22 |
14 |
p. 3753-3772
20 p.
|
artikel
|
| 23 |
Triglyceride-lowering agents
|
Salakhutdinov, Nariman F.
|
|
2014
|
22 |
14 |
p. 3551-3564
14 p.
|
artikel
|
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